REG - Indivior PLC - 1st Quarter Results
29/04/2021 12:00
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RNS Number : 0556X Indivior PLC 29 April 2021
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April 29, 2021
Q1 2021 Results Announced; FY 2021 Guidance Reiterated.
Quarter to March 31 2021 2020
$m $m
Net Revenue 180 153
Operating Profit/(Loss) 57 (189)
Net Income/(Loss) 80 (163)
EPS/(LPS) (cents per share) 11 (22)
Adjusted Operating Profit* 51 3
Adjusted Net Income/(Loss)* 38 (3)
Adjusted EPS* (cents per share) 5 -
(*)Adjusted (Adj.) basis excludes the impact of exceptional items as
referenced in Notes 3 and 4.
Comment by Mark Crossley, CEO of Indivior PLC
"We have seen an encouraging start in FY 2021 with growth in net revenue,
operating profit and cash from execution against our strategic priorities.
Despite the ongoing impacts of COVID-19, SUBLOCADE® (buprenorphine
extended-release) injection achieved solid net revenue growth both on a
sequential and year-over-year basis, and we expanded our Organized Health
Systems (OHS) platform to build the foundation for future growth. Looking
ahead, we are seeing healthcare restrictions in the US begin to ease from the
rapid pace of COVID-19 vaccinations, which supports our expectation of
increased in-person interactions with healthcare practitioners in the second
half of the year. As such, we are reiterating our FY 2021 base case guidance."
Q1 2021 Financial Highlights
· Net revenue (NR) of $180m (+18% vs. Q1 2020) primarily benefited
from higher NR from SUBLOCADE, continued growth in the buprenorphine
medication-assisted (BMAT) market and relative market share stability in the
US for SUBOXONE® (buprenorphine and naloxone) Film.
· Reported operating profit of $57m (Q1 2020 op. loss: $189m).
Excluding exceptional benefits of $6m, adjusted operating profit was $51m
(adj. Q1 2020: $3m). The increase over the prior period reflects higher NR and
lower SG&A expense principally related to the direct-to-consumer (DTC)
advertising campaign for SUBLOCADE in Q1 2020 and lower legal costs primarily
due to resolving the Department of Justice (DOJ) matter.
· Reported net income was $80m which includes an exceptional tax
benefit of $36m recognized in relation to development credits for SUBLOCADE.
Adjusted net income of $38m (Q1 2020 adj. net loss: $3m), primarily reflecting
higher operating profit as described above.
· Cash of $945m at the end of Q1 2021 (+$87m vs. FY 2020). Net cash
of $711m (+$88m vs. FY 2020). The higher cash balance primarily reflects the
timing of government rebate payables related to SUBOXONE Film and $26m of cash
collateral returned by a surety bond holder.
Q1 2021 Operating Highlights
· SUBLOCADE NR of $43m (+48% vs. Q1 2020 and +10% vs. Q4 2020);
strong growth in the OHS channel, new US patient enrollments increasing and
favorable trade spend accrual updates. Q1 2021 US dispenses approx. 35,700
units (+51% vs. Q1 2020 and +11% vs. Q4 2020).
· PERSERIS® (risperidone) extended-release injection NR of $3m
(unchanged vs. Q1 2020 and -25% vs. Q4 2020).
· SUBOXONE® Film share averaged 20% in Q1 2021 (Q1 2020: 22%) and
exited Q1 2021 at 20% (Q1 2020: 22%).
Reiterating FY 2021 Guidance
FY 2021 guidance issued by Indivior on February 18, 2021 is unchanged.
U.S. Opioid Use Disorder (OUD) Market Update
In Q1 2021, growth of the U.S. buprenorphine medication-assisted treatment
(BMAT) market was 6%. The moderation in the growth rate versus 2020 reflects
the high base period for comparison in the year-ago quarter, when the BMAT
market grew in the low- to mid-teens as a result of COVID-19-related demand
and the implementation of new federal and state government actions to
facilitate access to medication-assisted treatment (MAT) for OUD patients.
The Group continues to expect long-term U.S. market growth to be sustained in
the high single-digit to low double-digit percentage range due to increased
overall public awareness of the opioid epidemic and approved treatments,
together with regulatory and legislative actions that have expanded OUD
treatment funding and treatment capacity. The number of physicians, nurse
practitioners and physician assistants who have received a waiver to
administer MAT and those able to treat up to the permitted level of 275
patients continued to grow in Q1 2021. As a result, there is increasing
patient access to BMAT. Indivior supports efforts to encourage more eligible
healthcare practitioners (HCPs) to provide BMAT, and the Group continues to
resource its compliance capabilities for the growing number of BMAT
prescribers and patients.
The Group's focus is to continue to expand access to SUBLOCADE amongst OHS and
core HCPs, in order to ensure availability of this potentially important
treatment option to the estimated 1 million+ patients per month who are
prescribed BMAT by HCPs.
Financial Performance in Q1 2021
Total net revenue in Q1 2021 increased 18% to $180m (Q1 2020: $153m) at actual
exchange rates and by 14% at constant FX.
U.S. net revenue increased 25% to $131m (Q1 2020: $105m). Growth in the
overall U.S. BMAT market was in-line with Group expectations discussed above
("U.S. Market Update"). Underlying market growth, together with SUBLOCADE net
revenue growth of 38% to $40m (Q1 2020: $29m), relative stability in SUBOXONE
Film share (avg. Q1 2021: 20% vs. avg. Q1 2020: 22%) and favorable trade spend
accrual updates drove the net revenue increase. PERSERIS net revenue was flat
year-on-year at $3m (Q1 2020: $3m).
Rest of World net revenue increased 2% at actual exchange rates to $49m (Q1
2020: $48m) and -8% at constant FX. ROW SUBLOCADE net revenue contributed $3m
in the Q1 2021 period. This benefit along with favourable foreign currency
translation was partially offset by continued austerity measures and generic
competition in Western European markets.
Gross margin as reported was 82% (Q1 2020: 85%). On an adjusted basis,
excluding $7m of exceptional costs related to inventory provisions due to the
adverse impact of COVID-19, Q1 2020 gross margin was 90%. The expected gross
margin decline on a reported and adjusted basis reflects unfavourable product
mix due to the continued market share resilience of SUBOXONE film, which is
less profitable due to the high proportion of revenue now coming from
government channels.
SG&A expenses as reported were $82m (Q1 2020: $309m). Q1 2021 SG&A
expenses included an exceptional $5m release of DOJ related matters provisions
and a benefit of $1m related to the out-licensing of nasal naloxone patents.
Q1 2020 SG&A included exceptional costs of $185m. The exceptional costs
comprised $183m related to the Department of Justice (DOJ) matter and $2m for
restructuring-related lease impairments.
On an adjusted basis, Q1 2021 SG&A expenses decreased 29% to $88m (Q1
2020: $124m). The decrease reflects lower marketing expenses, mainly resulting
from the Q1 2020 U.S. DTC television advertising campaign for SUBLOCADE, as
well as a decline in legal expenses following the resolution with the DOJ in
2020. The year-ago period benefitted from Executive Committee members forgoing
any bonus payment associated with the Group's Annual Incentive Bonus Plan
(AIP).
R&D expenses were $9m (Q1 2020: $10m). Both periods primarily reflect
R&D activities as part of the completed strategic alignment to principally
support SUBLOCADE Health Economics and Outcomes Research (HEOR) and
post-marketing study commitments for SUBLOCADE and PERSERIS, as well as lower
than expected investments for supply-related projects.
Operating profit as reported was $57m (Q1 2020 op. loss: $189m). Exceptional
benefits of $6m are included in the current period. Exceptional costs of $192m
were included in the Q1 2020 results.
On an adjusted basis, Q1 2021 operating profit was $51m versus $3m in Q1 2020.
The increase primarily reflects higher net revenue along with the decrease in
operating expenses (principally SG&A) related to the promotional
initiatives for SUBLOCADE (primarily the DTC campaign) in the prior-year
period and lower legal expenses following the DOJ resolution in 2020.
Net finance expense in the quarter was $4m (Q1 2020 net finance expense: $2m).
The net expense primarily reflects lower interest income on the Group's cash
balance due to lower short-term interest rates versus the year-ago period and
additional interest expense associated with legal provisions/liabilities.
Tax benefit in the quarter was $27m at a rate of -51% (Q1 2020 tax benefit:
$28m, 15%). On an adjusted basis, excluding a $36m tax exceptional benefit for
the approval of prior year orphan drug credits, Q1 2021 tax expense was $9m at
a rate of 19% (Q1 2020 a non-meaningful rate excluding $32m of tax benefits on
exceptional costs).
Net income was $80m (Q1 2020 net loss: $163m), and $38m on an adjusted basis
excluding the $42m after-tax impact from exceptional items (Q1 2020 adj. net
loss: $3m). Q1 2020 adjusted net loss excludes $160m after-tax impact from
exceptional items.
Basic earnings per share was 11 cents and 5 cents on an adjusted basic basis
(Q1 2020 basic loss per share of 22 cents and nil on an adjusted basis).
Balance Sheet & Cash Flow
Cash and cash equivalents at the end of Q1 2021 were $945m (FY 2020: $858m).
Borrowings, net of issuance costs, were $234m at the end of Q1 2021 (FY 2020:
$235m). As a result, net cash stood at $711m at the end of Q1 2021 (FY 2020:
$623m).
Net working capital (inventory plus trade receivables and other assets, less
trade and other payables) was negative $250m at the end of Q1 2021 versus
negative $202m at the end of FY 2020. The $48m change in the period was
primarily driven by $26m of cash collateral returned by a surety bond holder.
Trade and other payables remained relatively unchanged primarily due sustained
government rebate payables related to SUBOXONE Film.
Cash generated from operations in Q1 2021 was $95m (Q1 2020 cash used in
operations: $141m), a change of $236m primarily due positive Q1 2021 operating
profit, timing of government rebate payables related to SUBOXONE Film and $26m
of cash collateral returned by a surety bond holder. Net cash inflow from
operating activities was $89m in the quarter (Q1 2020 net cash outflow: $146m)
reflecting the higher cash from operating activities and tax and interest
payments in the quarter.
Q1 2021 cash inflow from investing activities was $1m (Q1 2020: nil)
reflecting proceeds received from out-licensing of nasal naloxone patents.
Q1 2021 cash outflow from financing activities was $3m (Q1 2020: $2m),
reflecting the principal portion of lease payments and the quarterly
amortisation on the term loan facility. In Q1 2020 cash used in financing
activities was partially offset by proceeds from issuance of shares to satisfy
the vesting of options under an employee stock purchase plan.
R&D / Pipeline Update
Indivior's quarterly R&D and pipeline update may be found
at: http://www.indivior.com/research-and-development/
(http://www.indivior.com/research-and-development/) .
Principal Risk Factors
The Group utilizes a formal process to identify, evaluate and manage
significant risks. The Directors have reviewed the principal risks and
uncertainties for the remainder of the 2021 financial year and do not consider
there to be any changes from those reported within the 2020 Indivior PLC
Annual Report. The principal risks and uncertainties affecting the Group's
business activities are detailed on pages 38 to 45 of the 2020 Indivior PLC
Annual Report. These include the following: business operations; product
pipeline, regulatory and safety; commercialization; economic and financial;
supply; legal and intellectual property; and compliance. Please click here
(http://www.indivior.com/annual-reports/) to access the report or go to
www.indivior.com/annual-reports/.
Exchange Rates
The average and period end exchange rates used for the translation of
currencies into U.S. dollars that have most significant impact on the Group's
results were:
Q1 2021 Q1 2020
GB £ period end 1.3778 1.2460
GB £ average rate 1.3785 1.2820
€ Euro period end 1.1774 1.1143
€ Euro average 1.2069 1.1026
Webcast Details
There will be a webcast today (April 29, 2021) at 1:00 PM BST (8:00 am EDT)
hosted by Mark Crossley, CEO. The details are below. All required materials
are available on the Group's website at www.indivior.com
(http://www.indivior.com) .
Webcast link:
https://edge.media-server.com/mmc/p/k5suipmj
(https://edge.media-server.com/mmc/p/k5suipmj)
Confirmation Code: 7968136
Participants, Local - London, United Kingdom: +44 (0) 2071 928338
Participants, Local - New York, United States of America: +1 646 741 3167
For Further Information
Investor Enquiries Jason Thompson VP Investor Relations, Indivior PLC +1 804 402 7123
jason.thompson@indivior.com
Media Enquiries Jonathan Sibun Tulchan Communications +44 207 353 4200
+1 804 594 0836
US Media Inquiries
Indiviormediacontacts@indivior.com
Corporate Website www.indivior.com
This announcement does not constitute an offer to sell, or the solicitation of
an offer to subscribe for or otherwise acquire or dispose of shares in the
Group to any person in any jurisdiction to whom it is unlawful to make such
offer or solicitation.
Forward-Looking Statements
This announcement contains certain statements that are forward-looking. By
their nature, forward-looking statements involve risks and uncertainties as
they relate to events or circumstances that may or may not occur in the
future. Actual results may differ materially from those expressed or implied
in such statements because they relate to future events. Forward-looking
statements include, among other things, statements regarding the Indivior
Group's financial guidance for 2021 and its medium- and long-term growth
outlook, its operational goals, its product development pipeline and
statements regarding ongoing litigation and other statements containing the
words "subject to", "believe", "anticipate", "plan", "expect", "intend",
"estimate", "project", "may", "will", "should", "would", "could", "can", the
negatives thereof, variations thereon and similar expressions.
Various factors may cause differences between Indivior's expectations and
actual results, including, among others (including those described in the risk
factors described in the most recent Indivior PLC Annual Report and in
subsequent releases): factors affecting sales of Indivior Group's products and
financial position; the outcome of research and development activities;
decisions by regulatory authorities regarding the Indivior Group's drug
applications or authorizations; the speed with which regulatory
authorizations, pricing approvals and product launches may be achieved, if at
all; the outcome of post-approval clinical trials; competitive developments;
difficulties or delays in manufacturing and in the supply chain; disruptions
in or failure of information technology systems; the impact of existing and
future legislation and regulatory provisions on product exclusivity; trends
toward managed care and healthcare cost containment; legislation or regulatory
action affecting pharmaceutical product pricing, reimbursement or access;
challenges in the commercial execution; claims and concerns that may arise
regarding the safety or efficacy of the Indivior Group's products and product
candidates; risks related to legal proceedings, including compliance with the
Group's agreements with the U.S. Department of Justice and with the Office of
Inspector General of the Department of Health and Human Services,
noncompliance with which could result in potential exclusion from U.S. Federal
health care programs; the ongoing investigative and antitrust litigation
matters; the opioid multi-district litigation; the Indivior Group's ability to
protect its patents and other intellectual property; the outcome of patent
infringement litigation relating to Indivior Group's products, including the
ongoing ANDA lawsuits; changes in governmental laws and regulations; issues
related to the outsourcing of certain operational and staff functions to third
parties; risks related to the evolving COVID-19 pandemic and the potential
impact of COVID-19 on the Indivior Group's operations and financial condition,
which cannot be predicted with confidence; uncertainties related to general
economic, political, business, industry, regulatory and market conditions; and
the impact of acquisitions, divestitures, restructurings, internal
reorganizations, product recalls and withdrawals and other unusual items.
Consequently, forward-looking statements speak only as of the date that they
are made and should be regarded solely as our current plans, estimates and
beliefs. You should not place undue reliance on forward-looking statements. We
cannot guarantee future results, events, levels of activity, performance, or
achievements. Except as required by law, we do not undertake and specifically
decline any obligation to update, republish or revise forward-looking
statements to reflect future events or circumstances or to reflect the
occurrences of unanticipated events.
SUBOXONE® (BUPRENORPHINE AND NALOXONE) SUBLINGUAL FILM (CIII)
Indication
SUBOXONE (buprenorphine and naloxone) Sublingual Film (CIII) is a prescription
medicine indicated for treatment of opioid dependence and should be used as
part of a complete treatment plan to include counseling and psychosocial
support.
Treatment should be initiated under the direction of healthcare providers
qualified under the Drug Addiction Treatment Act.
Important Safety Information
Do not take SUBOXONE Film if you are allergic to buprenorphine or naloxone as
serious negative effects, including anaphylactic shock, have been reported.
SUBOXONE Film can be abused in a manner similar to other opioids, legal or
illicit.
SUBOXONE Film contains buprenorphine, an opioid that can cause physical
dependence with chronic use. Physical dependence is not the same as addiction.
Your healthcare provider can tell you more about the difference between
physical dependence and drug addiction. Do not stop taking SUBOXONE Film
suddenly without talking to your healthcare provider. You could become sick
with uncomfortable withdrawal symptoms because your body has become used to
this medicine.
SUBOXONE Film can cause serious life-threatening breathing problems, overdose
and death, particularly when taken by the intravenous (IV) route in
combination with benzodiazepines or other medications that act on the nervous
system (i.e., sedatives, tranquilizers, or alcohol). It is extremely dangerous
to take nonprescribed benzodiazepines or other medications that act on the
nervous system while taking SUBOXONE Film.
You should not drink alcohol while taking SUBOXONE Film, as this can lead to
loss of consciousness or even death.
Death has been reported in those who are not opioid dependent.
Your healthcare provider may monitor liver function before and during
treatment.
SUBOXONE Film is not recommended in patients with severe hepatic impairment
and may not be appropriate for patients with moderate hepatic impairment.
However, SUBOXONE Film may be used with caution for maintenance treatment in
patients with moderate hepatic impairment who have initiated treatment on a
buprenorphine product without naloxone.
Keep SUBOXONE Film out of the sight and reach of children. Accidental or
deliberate ingestion of SUBOXONE Film by a child can cause severe breathing
problems and death.
Do not take SUBOXONE Film before the effects of other opioids (e.g., heroin,
hydrocodone, methadone, morphine, oxycodone) have subsided as you may
experience withdrawal symptoms.
Injecting the SUBOXONE Film product may cause serious withdrawal symptoms such
as pain, cramps, vomiting, diarrhea, anxiety, sleep problems, and cravings.
Before taking SUBOXONE Film, tell your healthcare provider if you are pregnant
or plan to become pregnant. If you are pregnant, tell your healthcare provider
as withdrawal signs and symptoms should be monitored closely and the dose
adjusted as necessary. If you are pregnant or become pregnant while taking
SUBOXONE Film, alert your healthcare provider immediately and you should
report it using the contact information provided below.
Opioid‐dependent women on buprenorphine maintenance therapy may require
additional analgesia during labour.
Neonatal opioid withdrawal syndrome (NOWS) is an expected and treatable
outcome of prolonged use of opioids during pregnancy, whether that use is
medically authorized or illicit. Unlike opioid withdrawal syndrome in adults,
NOWS may be life-threatening if not recognized and treated in the neonate.
Healthcare professionals should observe newborns for signs of NOWS and manage
accordingly.
Before taking SUBOXONE Film, talk to your healthcare provider if you are
breastfeeding or plan to breastfeed your baby. The active ingredients of
SUBOXONE Film can pass into your breast milk. You and your healthcare provider
should consider the development and health benefits of breastfeeding along
with your clinical need for SUBOXONE Film and should also consider any
potential adverse effects on the breastfed child from the drug or from the
underlying maternal condition.
Do not drive, operate heavy machinery, or perform any other dangerous
activities until you know how SUBOXONE Film affects you. Buprenorphine in
SUBOXONE Film can cause drowsiness and slow reaction times during
dose-adjustment periods.
Common side effects of SUBOXONE Film include nausea, vomiting, drug withdrawal
syndrome, headache, sweating, numb mouth, constipation, painful tongue,
redness of the mouth, intoxication (feeling lightheaded or drunk), disturbance
in attention, irregular heartbeat, decrease in sleep, blurred vision, back
pain, fainting, dizziness, and sleepiness.
This is not a complete list of potential adverse events associated with
SUBOXONE Film. Please see full Prescribing Information www.suboxoneREMS.com
(http://www.suboxoneREMS.com) for a complete list.
*To report pregnancy or side effects associated with taking SUBOXONE Film,
please call 1-877-782-6966. You are encouraged to report negative side effects
of prescription drugs to the FDA. Visit www.fda.gov/medwatch
(http://www.fda.gov/medwatch) or call 1-800-FDA-1088
For more information about SUBOXONE Film, SUBOXONE (buprenorphine and
naloxone) Sublingual Tablets (CIII), or SUBUTEX(®) (buprenorphine) Sublingual
Tablets (CIII), please see the respective full Prescribing Information and
Medication Guide at www.suboxoneREMS.com (http://www.suboxoneREMS.com) .
SUBLOCADE (buprenorphine extended-release) injection, for subcutaneous use
(CIII)
INDICATION AND HIGHLIGHTED SAFETY INFORMATION
INDICATION
SUBLOCADE is indicated for the treatment of moderate to severe opioid use
disorder in patients who have initiated treatment with a transmucosal
buprenorphine-containing product, followed by dose adjustment for a minimum of
7 days.
SUBLOCADE should be used as part of a complete treatment plan that includes
counseling and psychosocial support.
HIGHLIGHTED SAFETY INFORMATION
WARNING: RISK OF SERIOUS HARM OR DEATH WITH INTRAVENOUS ADMINISTRATION;
SUBLOCADE RISK EVALUATION AND MITIGATION STRATEGY
● Serious harm or death could result if administered
intravenously. SUBLOCADE forms a solid mass upon contact with body fluids and
may cause occlusion, local tissue damage, and thrombo-embolic events,
including life threatening pulmonary emboli, if administered intravenously.
● Because of the risk of serious harm or death that could
result from intravenous self-administration, SUBLOCADE is only available
through a restricted program called the SUBLOCADE REMS Program.
Healthcare settings and pharmacies that order and dispense SUBLOCADE must be
certified in this program and comply with the REMS requirements.
Prescription use of this product is limited under the Drug Addiction Treatment
Act.
CONTRAINDICATIONS
SUBLOCADE should not be administered to patients who have been shown to be
hypersensitive to buprenorphine or any component of the ATRIGEL® delivery
system
WARNINGS AND PRECAUTIONS
Addiction, Abuse, and Misuse: SUBLOCADE contains buprenorphine, a Schedule
III controlled substance that can be abused in a manner similar to other
opioids. Monitor patients for conditions indicative of diversion or
progression of opioid dependence and addictive behaviors.
Respiratory Depression: Life threatening respiratory depression and death
have occurred in association with buprenorphine. Warn patients of the
potential danger of self-administration of benzodiazepines or other CNS
depressants while under treatment with SUBLOCADE.
Opioids can cause sleep-related breathing disorders e.g., central sleep apnea
(CSA), sleep-related hypoxemia. Opioid use increases the risk of CSA in a
dose-dependent fashion. Consider decreasing the opioid using best practices
for opioid taper if CSA occurs.
Strongly consider prescribing naloxone at SUBLOCADE initiation or renewal
because patients being treated for opioid use disorder have the potential for
relapse, putting them at risk for opioid overdose. Educate patients and
caregivers on how to recognize respiratory depression and how to treat with
naloxone if prescribed.
Risk of Serious Injection Site Reactions: The most common injection site
reactions are pain, erythema and pruritis with some involving abscess,
ulceration, and necrosis. The likelihood of serious injection site reactions
may increase with inadvertent intramuscular or intradermal administration.
Neonatal Opioid Withdrawal Syndrome: Neonatal opioid withdrawal syndrome is
an expected and treatable outcome of prolonged use of opioids during
pregnancy.
Adrenal Insufficiency: If diagnosed, treat with physiologic replacement of
corticosteroids, and wean patient off the opioid.
Risk of Opioid Withdrawal With Abrupt Discontinuation: If treatment with
SUBLOCADE is discontinued, monitor patients for several months for withdrawal
and treat appropriately.
Risk of Hepatitis, Hepatic Events: Monitor liver function tests prior to and
during treatment.
Risk of Withdrawal in Patients Dependent on Full Agonist Opioids: Verify that
patient is clinically stable on transmucosal buprenorphine before injecting
SUBLOCADE.
Treatment of Emergent Acute Pain: Treat pain with a non-opioid analgesic
whenever possible. If opioid therapy is required, monitor patients closely
because higher doses may be required for analgesic effect.
ADVERSE REACTIONS
Adverse reactions commonly associated with SUBLOCADE (in ≥5% of subjects)
were constipation, headache, nausea, injection site pruritus, vomiting,
increased hepatic enzymes, fatigue, and injection site pain.
For more information about SUBLOCADE, the full Prescribing Information
including BOXED WARNING, and Medication Guide, visit www.sublocade.com
(file:///C:/Users/jthompson/Desktop/Earnings/Q1%202021/Release/www.sublocade.com)
.
PERSERIS® (risperidone) for extended-release injectable suspension
INDICATION AND HIGHLIGHTED SAFETY INFORMATION
PERSERIS (risperidone) is indicated for the treatment of schizophrenia in
adults.
WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED
PSYCHOSIS
See full prescribing information for complete boxed warning.
• Elderly patients with dementia-related psychosis treated
with antipsychotic drugs are at an increased risk of death.
• PERSERIS is not approved for use in patients with
dementia-related psychosis.
CONTRAINDICATIONS
PERSERIS should not be administered to patients with known hypersensitivity to
risperidone, paliperidone, or other components of PERSERIS.
WARNINGS AND PRECAUTIONS
Cerebrovascular Adverse Reactions, Including Stroke in Elderly Patients with
Dementia-Related Psychosis: Increased risk of cerebrovascular adverse
reactions (e.g., stroke, transient ischemic attack), including fatalities.
PERSERIS is not approved for use in patients with dementia-related psychosis.
Neuroleptic Malignant Syndrome (NMS): Manage with immediate discontinuation
and close monitoring.
Tardive Dyskinesia: Discontinue treatment if clinically appropriate.
Metabolic Changes: Monitor for hyperglycemia, dyslipidemia and weight gain.
Hyperprolactinemia: Prolactin elevations occur and persist during chronic
administration. Long-standing hyperprolactinemia, when associated with
hypogonadism, may lead to decreased bone density in females and males.
Orthostatic Hypotension: Monitor heart rate and blood pressure and warn
patients with known cardiovascular disease or cerebrovascular disease, and
risk of dehydration or syncope.
Leukopenia, Neutropenia, and Agranulocytosis: Perform complete blood counts
(CBC) in patients with a history of a clinically significant low white blood
cell count (WBC) or history of leukopenia or neutropenia. Consider
discontinuing PERSERIS if a clinically significant decline in WBC occurs in
absence of other causative factors.
Potential for Cognitive and Motor Impairment: Use caution when operating
machinery.
Seizures: Use caution in patients with a history of seizures or with
conditions that lower the seizure threshold.
ADVERSE REACTIONS
The most common adverse reactions in clinical trials (≥ 5% and greater than
twice placebo) were increased weight, sedation/somnolence and musculoskeletal
pain. The most common injection site reactions (≥ 5%) were injection site
pain and erythema (reddening of the skin).
For more information about PERSERIS, the full Prescribing Information
including BOXED WARNING, and Medication Guide visit www.perseris.com
(http://www.perseris.com) .
Condensed consolidated interim income statement
For the three months ended March 31 Notes Unaudited Unaudited
2021 2020
$m $m
Net Revenues 2 180 153
Cost of sales (32) (23)
Gross Profit 148 130
Gross profit before exceptional items 4 148 137
Exceptional items 3 - (7)
Selling, general and administrative expenses 3 (82) (309)
Research and development expenses 3 (9) (10)
Operating Profit/(Loss) 57 (189)
Operating profit before exceptional items 4 51 3
Exceptional items 3 6 (192)
Finance income 2 4
Finance expense (6) (6)
Net finance expense (4) (2)
Profit/(Loss) Before Taxation 53 (191)
Income tax benefit 27 28
Taxation before exceptional items 5 (9) (4)
Exceptional items within taxation 3,5 36 32
Net Income/(loss) 80 (163)
Earnings/(loss) per ordinary share (cents)
Basic earnings/(loss) per share 6 11 (22)
Diluted earnings/(loss) per share 6 10 (22)
Condensed consolidated interim statement of comprehensive income/(loss)
For the three months ended March 31 Unaudited Unaudited
2021
2020
$m
$m
Net income/(loss) 80 (163)
Other comprehensive income/(loss)
Items that may be reclassified to profit or loss in subsequent years:
Net exchange adjustments on foreign currency translation
1 (10)
Other comprehensive income/(loss) 1 (10)
Total comprehensive income/(loss) 81 (173)
The notes are an integral part of these condensed consolidated interim
financial statements.
Condensed consolidated interim balance sheet
Unaudited Audited
Mar 31, 2021 Dec 31, 2020
Notes $m $m
ASSETS
Non-current assets
Intangible assets 60 62
Property, plant and equipment 59 60
Right-of-use assets 41 43
Deferred tax assets 81 75
Other assets 7 103 104
344 344
Current assets
Inventories 91 93
Trade receivables 165 179
Other assets 7 23 50
Current tax receivable 5 43 7
Cash and cash equivalents 8 945 858
1,267 1,187
Total assets 1,611 1,531
LIABILITIES
Current liabilities
Borrowings 8 (4) (4)
Provisions and other liabilities 9 (89) (48)
Trade and other payables 12 (529) (524)
Lease liabilities (8) (8)
Current tax liabilities 5 (26) (15)
(656) (599)
Non-current liabilities
Borrowings 8 (229) (230)
Provisions and other liabilities 9 (521) (577)
Lease liabilities (41) (43)
(791) (850)
Total liabilities (1,447) (1,449)
Net assets 164 82
EQUITY
Capital and reserves
Share capital 13 73 73
Share premium 6 6
Other Reserves (1,295) (1,295)
Foreign currency translation reserve (12) (13)
Retained earnings 1,392 1,311
Total equity 164 82
The notes are an integral part of these condensed consolidated interim
financial statements.
Condensed consolidated interim statement of changes in equity
Share Share Other Foreign Retained Total equity
capital premium reserve currency earnings
translation
reserve
Unaudited $m $m $m $m $m $m
Balance at January 1, 2021 73 6 (1,295) (13) 1,311 82
Comprehensive income
Net income - - - - 80 80
Other comprehensive income - - - 1 - 1
Total comprehensive income - - - 1 80 81
Transactions recognised directly in equity
Share-based plans - - - - 1 1
Balance at March 31, 2021 73 6 (1,295) (12) 1,392 164
Balance at January 1, 2020 73 5 (1,295) (23) 1,449 209
Comprehensive loss
Net loss - - - - (163) (163)
Other comprehensive loss - - - (10) - (10)
Total comprehensive loss - - - (10) (163) (173)
Transactions recognised directly in equity
Share-based plans - 1 - - 2 3
Balance at March 31, 2020 73 6 (1,295) (33) 1,288 39
The notes are an integral part of these condensed consolidated interim
financial statements.
Condensed consolidated interim cash flow statement
For the three months ended March 31 Unaudited Unaudited
2021 2020
$m $m
CASH FLOWS FROM OPERATING ACTIVITIES
Operating Profit/(Loss) 57 (189)
Depreciation, amortization, and impairment 3 6
Depreciation and impairment of right-of-use assets 2 3
Gain on disposal of ROU assets - (2)
Gain on disposal of intangible assets (1) -
Share-based payments - 2
Impact from foreign exchange movements - 5
Decrease in trade receivables 13 36
Decrease/(Increase) in other assets 28 (44)
Decrease/(increase) in inventories 3 (7)
Increase/(decrease) in trade and other payables 7 (133)
(Decrease)/increase in provisions* (17) 182
Cash generated from/(used in) operations 95 (141)
Interest paid (4) (5)
Interest received - 4
Taxes paid (2) (4)
Net cash inflow/(outflow) from operating activities 89 (146)
CASH FLOWS FROM INVESTING ACTIVITIES
Proceeds from disposal of intangible assets 1 -
Net cash inflow from investing activities 1 -
CASH FLOWS FROM FINANCING ACTIVITIES
Repayment of borrowings (1) (1)
Payment of lease liabilities (2) (2)
Proceeds from the issuance of ordinary shares - 1
Net cash outflow from financing activities (3) (2)
Net increase/(decrease) in cash and cash equivalents 87 (148)
Cash and cash equivalents at beginning of the period 858 1,060
Cash and cash equivalents at end of the period 945 912
* - Changes in provisions and other liabilities line includes an exceptional
payment of $10m to RB in accordance with the settlement agreement
The notes are an integral part of these condensed consolidated interim
financial statements.
Notes to the condensed consolidated interim financial statements
1. BASIS OF PREPARATION AND ACCOUNTING POLICIES
Indivior PLC (the 'Company') is a public limited company incorporated on
September 26, 2014 and domiciled in the United Kingdom. In these Condensed
consolidated interim financial statements ('Condensed Financial Statements'),
reference to the 'Group' means the Company and all its subsidiaries.
These Condensed Financial Statements have been prepared in conformity with
International accounting standard 34, 'Interim Financial Reporting', as
contained in UK-adopted international accounting standards ("IAS 34"). The
financial information herein has been prepared based on the accounting
policies set out in the annual accounts of the Group for the year ended
December 31, 2020 and should be read in conjunction with those annual
accounts. The Group prepared its annual accounts in accordance with
international accounting standards in conformity with the requirements of the
Companies Act 2006, and in accordance with International Financial Reporting
Standards adopted pursuant to Regulation (EC) No 1606/2002 as it applies in
the European Union (adopted IFRSs). In preparing these Condensed Financial
Statements, the significant judgments made by management in applying the
Group's accounting policies and the key sources of estimation uncertainty were
the same as those that applied to the consolidated financial statements for
the year ended December 31, 2020, with the exception of changes in estimates
that are required in determining the provision for income taxes. The Q1 2020
statement of cash flows has been expanded to present trade receivables and
other assets (current) in separate line items to improve the transparency and
consistency.
The Condensed Financial Statements do not include all the information and
disclosures required in the annual financial statements and should be read in
conjunction with the Group's annual financial statements as at December 31,
2020. These Condensed Financial Statements have been reviewed and not audited.
These Condensed Financial Statements were approved for issue on April 28,
2021.
As disclosed in Notes 9, 10 and 11, the Group has liabilities and provisions
totaling $555m (FY 2020: $568m) for the Department of Justice (DOJ) Resolution
and related matters and the Reckitt Benckiser (RB) settlement. The Directors
have assessed the Group's ability to comply with the financial covenants in
the Group's debt facility, maintain sufficient liquidity to fund its
operations, fulfill obligations under the DOJ and RB agreements, and address
the reasonably possible financial implications of the ongoing legal
proceedings. The Directors have modeled the risk that SUBLOCADE will not meet
revenue growth expectations due to the continued impact from the COVID-19
pandemic (considering a 15% decline on forecasts) as part of the Group's
going concern assessment and downside scenario. These risks were balanced
against the Group's current and forecast working capital position, impact of
the cost saving actions taken to date, and timing of the final
balloon payment on the term loan in Q4 2022 which is outside the going
concern assessment period. As a result of the factors set out above,
the Directors of the Group have a reasonable expectation that the Group has
adequate resources to continue in operational existence for at least one year
from the approval of these Condensed Financial Statements and therefore
consider it appropriate to adopt the going concern basis for accounting and
preparing these Condensed Financial Statements.
The financial information contained in this document does not constitute
statutory accounts as defined in section 434 and 435 of the Companies Act
2006. The Group's statutory financial statements for the year ended December
31, 2020 were approved by the Board of Directors on March 18, 2021 and will be
delivered to the Registrar of Companies.
2. SEGMENT INFORMATION
Operating segments are reported in a manner consistent with the internal
reporting provided to the chief operating decision-maker ('CODM'). The CODM,
who is responsible for allocating resources and assessing performance of the
operating segments, has been identified as the Chief Executive Officer (CEO).
The Group is predominantly engaged in a single business activity, which is the
development, manufacture and sale of buprenorphine-based prescription drugs
for treatment of opioid dependence and related disorders. The CEO reviews
disaggregated net revenue on a geographical and product basis. Financial
results are reviewed on a consolidated basis for evaluating financial
performance and allocating resources. Accordingly, the Group operates in a
single reportable segment.
Net revenues
Revenues are attributed to countries based on the country where the sale
originates. The following table represents net revenues from continuing
operations and non-current assets, net of accumulated depreciation and
amortization, by country. Non-current assets for this purpose consist of
intangible assets, property, plant and equipment, right-of-use assets, and
other assets. Net revenues and non-current assets for the three months to
March 31, 2021 and 2020 were as follows:
Net revenue:
For the three months ended March 31 2021 2020
$m $m
United States 131 105
Rest of World 49 48
Total net revenues 180 153
On a disaggregated basis, the Group's net revenue by major product line:
For the three months ended March 31 2021 2020
$m $m
Sublingual/other 134 121
SUBLOCADE 43 29
PERSERIS 3 3
Total 180 153
Non-current assets:
Mar 31, 2021 Dec 31, 2020
$m $m
United States 138 141
Rest of World 125 128
Total 263 269
3. OPERATING EXPENSES
The table below sets out selected operating expenses information:
For the three months ended March 31
2021 2020
$m $m
Research and development expenses (9) (10)
Selling and general expenses (37) (74)
Administrative expenses(1) (42) (229)
Depreciation, amortization and impairment(2) (3) (6)
Total (82) (309)
(1)Administrative expenses include exceptional items in the current and prior
period as outlined in the table below.
(2)Additional depreciation and amortization of $2m (2020: $3m) for intangibles
and ROU assets is included within cost of sales.
Exceptional Items
Where significant expenses or income occur that do not reflect the Group's
ongoing operations, these items are disclosed as exceptional items in the
income statement. Examples of such items could include restructuring and
related expenses for the reconfiguration of the Group's activities and/or
capital structure, impairment of current and non-current assets, certain costs
arising as a result of material and non-recurring regulatory and litigation
matters, and certain tax related matters.
The table below sets out exceptional items recorded in the quarter:
For the three months ended March 31
2021 2020
$m $m
Cost of sales(1) - (7)
Restructuring costs(2) - (2)
Legal expenses/provision(3) 5 (183)
Other operating income(4) 1 -
Total exceptional items before taxes 6 (192)
Tax benefit on exceptional items(3) - 32
Exceptional tax item(5) 36 -
Total exceptional items 42 (160)
1. $7m of exceptional cost of sales in Q1 2020 relate to inventory
provisions due to the adverse impact of Covid-19 on the business.
2. Restructuring costs in Q1 2020 consist primarily of lease
disposals. Restructuring costs are included in SG&A.
3. Negotiations with DOJ related plaintiffs in Q1 2021 led to a change
in the Group's provision for DOJ related matters which resulted in a provision
release of $5m. In Q1 2020, $183m of legal costs and an exceptional tax
benefit of $32m were recorded in relation to the DOJ Resolution. Exceptional
legal costs are included within SG&A.
4. Exceptional income in Q1 2021 relates to the proceeds received from
the out-licensing of nasal naloxone opioid overdose patents which are included
within SG&A.
5. $36m exceptional tax benefit item relates to the approval of tax
credits by the Internal Revenue Service in relation to development credits for
SUBLOCADE claimed for years 2014 to 2017.
4. ADJUSTED RESULTS
The Board and management team use adjusted results and measures to provide
incremental insight to the financial results of the Group and the way it is
managed. The tables below show the list of adjustments between the reported
and adjusted results for both Q1 2021 and 2020. Refer to Note 3 for more
information on exceptional items.
Reconciliation of gross profit to adjusted gross profit
For the three months ended March 31 2021 2020
$m $m
Gross profit 148 130
Exceptional cost of sales - 7
Adjusted gross profit 148 137
Reconciliation of operating profit/(loss) to adjusted operating profit
For the three months ended March 31 2021 2020
$m $m
Operating profit/(loss) 57 (189)
Exceptional cost of sales - 7
Exceptional selling, general and administrative expenses (6) 185
Adjusted operating profit 51 3
Reconciliation of profit/(loss) before taxation to adjusted profit before
taxation
For the three months ended March 31 2021 2020
$m $m
Profit/(loss) before taxation 53 (191)
Exceptional cost of sales - 7
Exceptional selling, general and administrative expenses (6) 185
Adjusted profit before taxation 47 1
Reconciliation of net income/(loss) to adjusted net income/(loss)
For the three months ended March 31 2021 2020
$m $m
Net income/(loss) 80 (163)
Exceptional cost of sales - 7
Exceptional selling, general and administrative expenses (6) 185
Tax benefit on exceptional items - (32)
Tax exceptional (36) -
Adjusted net income/(loss) 38 (3)
5. TAXATION
The Group calculates tax expense for interim periods using the expected full
year rates, considering the pre-tax income and statutory rates for each
jurisdiction. The resulting expense is allocated between current and deferred
taxes based upon the forecasted full year ratio.
In the three months ended March 31, 2021, the reported total tax benefit was
$27m, or a rate of -51% (Q1 2020 tax charge: $28m, 15%). On an adjusted basis
tax expense of $9m (Q1 2020: $4m) excluding tax exceptionals of $36m (Q1 2020:
tax benefit on exceptional costs $32m), on adjusted profit before tax of $47m
(Q1 2020: $1m) represented a 19% quarterly effective tax rate (Q1 2020: a
non-meaningful rate). The current period exceptional tax benefit of $36m
relates to the tax credit receivable in relation to development credits for
SUBLOCADE claimed in prior years.
The Group's balance sheet at March 31, 2021 includes a current tax receivable
of $43m (FY 2020: $7m), a current tax payable of $26m (FY 2020: $15m), and
deferred tax asset of $81m (FY 2020: $75m). The current tax receivable balance
has increased due to recording the receivable for SUBLOCADE development
credits and advance cash tax payments.
The change in the adjusted effective tax rate was primarily driven by the
relative contribution to pre-tax income by taxing jurisdiction in the quarter.
Other tax matters
The European Commission issued a press release on April 2, 2019 announcing its
conclusion that the United Kingdom ('UK') Finance Company Partial Exemption
Rules are partly justified. The UK government has made an annulment
application to the General Court against this decision. The UK government is
now required to initiate recovery of the alleged State Aid irrespective of any
appeal against the decision. The Group continues to monitor its position
regarding the potential State Aid challenge and based upon our fact pattern
has determined that no provision is required at this time. The Group has
benefited from the UK controlled foreign company financing exemption and the
tax thereon is approximately $25m including interest.
The enacted United Kingdom ("UK") Statutory Corporation Tax rate was 19% for
the year ended December 31, 2020. On March 3, 2021 the UK Chancellor announced
an increase in the corporation tax rate from 19% to 25% with effect from April
1, 2023. The rate is not substantively enacted or enacted at March 31, 2021.
The impact of the rate increase to the UK deferred tax assets held at March
31, 2021 would be less than $1m.
6. EARNINGS/(LOSS) PER SHARE
For the three months ended March 31 2021 2020
cents cents
Basic earnings/(loss) per share 11 (22)
Diluted earnings/(loss) per share 10 (22)
Adjusted basic earnings per share 5 -
Adjusted diluted earnings per share 5 -
Basic
Basic earnings/(loss) per share ("EPS" or "LPS") is calculated by dividing
profit/(loss) for the period attributable to owners of the Company by the
weighted average number of ordinary shares in issue during the period.
Diluted
Diluted earnings/(loss) per share is calculated by adjusting the weighted
average number of ordinary shares outstanding to assume conversion of all
dilutive potential ordinary shares. The Company has dilutive potential
ordinary shares in the form of stock options and awards. The weighted average
number of shares is adjusted for the number of shares granted assuming the
exercise of stock options.
Weighted average number of shares 2021 2020
Thousands thousands
On a basic basis 734,220 731,982
Dilution from share awards and options 47,124 45,106
On a diluted basis 781,344 777,088
Adjusted Earnings
The Directors believe that diluted earnings per share, adjusted for the impact
of exceptional items after the appropriate tax amount, provides more
meaningful information on underlying trends to shareholders in respect of
earnings per ordinary share. A reconciliation of net income to adjusted net
income is included in Note 4.
7. CURRENT AND NON-CURRENT OTHER ASSETS
Current and non-current other assets Mar 31 Dec 31
2021 2020
$m $m
Short-term prepaid expenses 17 17
Other current assets 6 33
Total other current assets 23 50
Long-term prepaid expenses 21 22
Other non-current assets 82 82
Total other non-current assets 103 104
Total 126 154
Other current and non-current assets as of December 31, 2020 primarily
represent the funding of surety bonds in relation to intellectual property
related matters (see Note 11 for further discussion). In Q1 2021, one of the
surety bond holders returned $26m causing a decrease in other current assets.
Long-term prepaid expenses relate primarily to payments for contract
manufacturing capacity.
8. FINANCIAL LIABILITIES - BORROWINGS
Bank loans Mar 31 Dec 31
2021 2020
$m $m
Bank loans - current (4) (4)
Bank loans - non-current (229) (230)
Total bank loans (233) (234)
Analysis of net debt Mar 31 Dec 31
2021 2020
$m $m
Cash and cash equivalents 945 858
Borrowings* (234) (235)
Total net cash 711 623
*Borrowings reflect the principal amount drawn before debt issuance costs of
$1m (FY 2020: $1m). These do not include lease liabilities of $49m (FY 2020:
$51m).
Reconciliation of net debt Mar 31 Dec 31
2021 2020
$m $m
The movements in the period were as follows:
Net cash at beginning of period 623 821
Net increase/(decrease) in cash and cash equivalents 87 (202)
Net repayment of borrowings 1 4
Net cash at end of period 711 623
Net cash is presented as it is relevant to our term loan maximum leverage
ratio. Net cash is not reduced for lease liabilities of $49m (FY 2020: $51m),
in accordance with the term loan ratio calculations.
At March 31, 2021, the term loan was trading at approximately 100% (FY 2020:
98%) of par value. Cash at bank, trade receivables, and trade payables are
assumed to approximate their fair values. The terms of the loan in effect at
March 31, 2021 are as follows:
Currency Nominal interest margin Maturity Required annual repayments Maximum leverage ratio
Term loan facility USD Libor* (1%) + 4.5% 2022 $4m 3.0
*The Term Loan matures after publication of LIBOR is expected to end. We have
engaged with the administrative agent and expect to work with other market
participants in the transition to a reasonable substitute base rate. No
financial impact is expected.
• Nominal interest margin is calculated over three-month LIBOR subject to
the LIBOR floor of 1%.
• The maximum leverage ratio (adjusted aggregated net debt divided by
Adjusted EBITDA) is a financial covenant to maintain net secured leverage
below 3.0x.
• A $50m revolving credit facility is available to the Group which remained
undrawn at the balance sheet date.
9. PROVISIONS AND OTHER LIABILITIES
Provisions & other liabilities Mar 31 Dec 31
2021 2020
$m $m
Provisions
DOJ related matters (27) (32)
Intellectual property related matters (48) (47)
Restructuring costs (3) (6)
Other (4) (4)
Total provisions (82) (89)
Other liabilities
DOJ resolution (488) (486)
RB indemnity settlement (40) (50)
Total other liabilities (528) (536)
Total provisions and other liabilities (610) (625)
The Group is involved in legal and intellectual property disputes as described
in Note 11, "Legal Proceedings."
Provisions
Provisions are recognized when the Group has a present legal or constructive
obligation as a result of past events, an outflow of resources to settle that
obligation is probable, and the amount can be reliably estimated. Provisions
are measured at the present value of management's best estimate of the
expenditure required to settle the present obligation at the reporting date.
The Group carries a provision of $27m (FY 2020: $32m) pertaining to DOJ
related matters as discussed in Note 11. Negotiations with DOJ related
plaintiffs resulted in an exceptional provision release of $5m in Q1 2021 (see
Note 3). DOJ related matters of $27m which are expected to be settled within
the year.
The Group carries provisions totaling $48m (FY 2020: $47m) for intellectual
property related matters, all of which relate to potential redress for ongoing
intellectual property litigation with DRL and Alvogen should the Group not be
successful with those cases outlined in Note 11, Intellectual property related
matters: ANDA litigation. The provision represents the Group's estimate of
potential damages for lost profits owed to DRL and Alvogen for the period
between FDA approval and lifting of the preliminary injunction based on
industry analogous for generic market share capture. Finance costs are
recognized in the income statement at an interest rate of 5.25%. In Q1 2021,
the Group recorded finance expense totaling $1m (Q1 2020: $1m). The Group does
not expect this matter to be settled within a year and therefore the provision
of $48m has been classified as non-current.
Other liabilities
Other liabilities represent contractual obligations to third parties where the
amount and timing of payments is fixed. Where other liabilities are not
interest-bearing and the impact of discounting is significant, other
liabilities are recorded at their present value, generally using rate
approximating the risk-free rate at the time the Group entered into the
obligation.
On July 24, 2020, the Group reached a resolution with the DOJ and other
litigants described in Note 11 under "DOJ Resolution", which was finalized in
November 2020 and the first payment of $103m (including interest) was made.
Subsequently, six annual instalments of $50m will be due every January 15 from
2022 to 2027 with the final instalment of $200m due in December 2027. Interest
accrues on certain portions of the resolution which will be paid together with
the annual instalment payments. For non-interest-bearing portions, the
liability has been recorded at the net present value based on timing of the
estimated payments. The discount rate and interest rate are 1.25%. In Q1 2021
the Group recorded interest expense totaling $2m (Q1 2020: nil). As of March
31, 2021, $51m has been classified as current on the Group's balance sheet.
On January 25, 2021, the Group reached a resolution with Reckitt Benckiser
(RB) to resolve claims which RB issued in the Commercial Court in London on
November 13, 2020, seeking indemnity under the 2014 Demerger Agreement.
Pursuant to the settlement, RB withdrew the US $1.4b claim to release Indivior
from any claim for indemnity under the Demerger Agreement relating to the DOJ
and FTC settlements which RB entered into in July 2019, as well as other
claims for indemnity arising from those matters. The Group has agreed to pay
RB a total of $50m and has agreed to release RB from any claims to seek
damages relating to its settlement with the DOJ and the FTC. The Group made a
$10m payment in February 2021, following the resolution. Subsequently, annual
instalment payments of $8m will be due every January from 2022 to 2026. The
Group carries a liability totaling $40m (FY 2020: $50m) related to this
settlement. The effect of discounting was not material.
10. CONTINGENT LIABILITIES
The Group has assessed certain legal and other matters to be not probable
based upon current facts and circumstances, including any potential impact the
DOJ resolution could have on these matters. These represent contingent
liabilities. Except for those matters discussed in Note 11 under "DOJ Related
Matters" and "Intellectual Property Related Matters", for which provisions
have been recognized, Note 11 sets out the contingent liabilities for legal
and other disputes for which the Group has assessed as contingent liabilities.
The Group has also assessed the State Aid matter discussed in Note 5 to be a
contingent liability.
11. LEGAL PROCEEDINGS
DOJ Resolution
Agreement to Resolve Criminal Charges and Civil Complaints Related to SUBOXONE
Film
· The Group settled with the United States Department of Justice
(Justice Department or DOJ), the U.S. Federal Trade Commission (FTC), and U.S.
state attorneys general the criminal and civil liability in connection with a
multi-count indictment brought in April 2019 by a grand jury in the Western
District of Virginia, a civil lawsuit joined by the Justice Department in
2018, and an FTC investigation. Under the terms of the resolution agreement
with the Justice Department, the Group has agreed to compliance terms
regarding its sales and marketing practices. Compliance with these terms is
subject to annual Board and CEO certifications submitted to the U.S.
Attorney's Office.
· As part of the resolution with the FTC and as detailed in the
text of the stipulated order, for a ten-year period Indivior Inc. is required
to make specified disclosures to the FTC and is prohibited from certain
conduct.
· Under the terms of the five-year Corporate Integrity Agreement
with the HHS Office of the Inspector General (HHS-OIG), the Group will
continue its commitment to promote compliance with laws and regulations and
its ongoing evolution of an effective compliance program, including written
standards, training, reporting, and monitoring procedures. The Group will be
subject to reporting and monitoring requirements, including annual reports and
compliance certifications from key management and the Board Nominating &
Governance Committee submitted to HHS-OIG. In addition, the Group will be
subject to monitoring by an Independent Review Organization, who will submit
audit findings to HHS-OIG, and review by a Board Compliance Expert, who will
prepare two compliance assessment reports in the first and third reporting
periods of the Corporate Integrity Agreement.
In November 2020, the Group made a payment of $103 million (including
interest) when the resolution was approved by a judge. Subsequently, six
annual instalments of $50 million will be due every January 15 from 2022
through 2027. The final instalment of $200 million will be due in December
2027. The Group carries a liability totaling of $488 million (FY 2020: $486m)
pertaining to the DOJ resolution.
DOJ Related Matters
Federal FCA Qui Tam Suits
· In August 2018, the United States unsealed three qui tam suits
pending in the Western District of Virginia that made a variety of allegations
under state and federal False Claims Act statutes regarding marketing and
promotion practices related to SUBOXONE, and in some instances claiming
unlawful retaliation. The suits also seek reasonable attorney's fees and
costs. Many of the civil claims concern the same conduct at issue in the
Superseding Indictment filed by the Justice Department. Indivior is aware of
additional claims pending in the District of New Jersey regarding similar
allegations about marketing and promotion practices which were resolved along
with the three Western District of Virginia qui tam suits in the federal civil
settlement agreement with the Justice Department; and resolved with the state
Attorney Generals in civil settlement agreements with the fifty states, D.C.,
and Puerto Rico. The Group is in discussions with certain relators aimed
toward resolving the retaliation claims and claims for attorney's fees and
costs.
State and Local Matters
· In October 2016, Indivior was served with a subpoena for records
from the State of Connecticut Office of the Attorney General under its
Connecticut civil false claims act authority. The subpoena requests documents
related to the Group's marketing and promotion of SUBOXONE products and its
interactions with a non-profit third-party organization. The Group has reached
an agreement to resolve this matter and has finalized the settlement
agreement.
· In November 2016, Indivior was served with a subpoena for records
from the State of California Department of Insurance under its civil
California insurance code authority. The subpoena requests documents related
to SUBOXONE® Film, SUBOXONE® Tablet, and SUBUTEX® Tablet. The State of
California served additional deposition subpoenas on Indivior in 2017 and
served a subpoena in 2018 requesting documents relating to the bioavailability
/ bioequivalency of SUBOXONE Film, manufacturing records for the product and
its components, and the potential to develop dependency on SUBOXONE Film. The
Group has fully cooperated in this civil investigation and is in discussions
aimed toward resolving the matter. Certain of the qui tam suits filed in the
Western District of Virginia and the District of New Jersey assert claims
under the civil California insurance code. The Group is in discussions toward
resolving these claims and claims for associated attorney's fees and costs.
· In June 2019, the Group learned that the State of Illinois
Insurance Department is investigating potential violations of its civil
Insurance Claims Fraud Prevention Act with respect to its sales and marketing
activity. Certain of the qui tam suits filed in the Western District of
Virginia and the District of New Jersey assert claims under this statute,
including claims for associated attorney's fees and costs. The Group is in
discussions aimed toward resolving this matter.
· In addition to the federal and state health program claims,
claims have been asserted under the city false claims acts of Chicago and New
York City regarding the promotion of Suboxone film. The Group has resolved the
matter with the City of Chicago.
False Claims Act Allegations
· In August 2018, the United States District Court for the Western
District of Virginia unsealed a declined qui tam complaint alleging causes of
action under the Federal and state False Claims Acts against certain entities
within the Group predicated on best price issues and claims of retaliation
(United States ex rel. Miller v. Reckitt Benckiser Group PLC et al., Case No.
1:15-cv-00017 (W.D. Va.)). The suit also seeks reasonable attorneys' fees and
costs. We understand that all government plaintiffs have declined to
intervene. The Group was served with the complaint in January 2021. We are in
discussions regarding this matter with the plaintiff-relator.
· In May 2018, Indivior Inc. received an informal request from the
Office of the United States Attorney for the Southern District of New York,
seeking records relating to the Suboxone manufacturing process. We are in
discussions with the government regarding the matter.
Securities Class Action Litigation
· In April 2019, Michael Van Dorp filed a putative class action
lawsuit in the United States District Court for the District of New Jersey on
behalf of holders of publicly traded Indivior securities alleging violations
of U.S. federal securities laws under the Securities Exchange Act of 1934. The
complaint names Indivior PLC, Shaun Thaxter, Mark Crossley and Cary J.
Claiborne as defendants. In February 2021, the parties reached a settlement
agreement. A Motion for Entry of Order Preliminarily Approving Settlement is
pending with the court.
Intellectual Property Related Matters
ANDA Litigation
· Litigation against DRL is currently pending in the District of
New Jersey regarding U.S. Patent No. 9,687,454 and 9,931,305 ("the '454 and
'305 Patents"). DRL received final FDA approval for all four strengths of its
generic buprenorphine/naloxone film product in June 2018, and immediately
launched its generic buprenorphine/naloxone film product "at-risk." In July
2018, the District Court issued a ruling granting Indivior a Preliminary
Injunction (PI) pending the outcome of a trial on the merits of the '305
Patent. Indivior was required to post a surety bond for $72 million in
connection with the PI. In November 2018, the CAFC issued a decision vacating
the PI against DRL. DRL launched its product at-risk in February 2019. In June
2019, DRL filed a motion for leave to file their first amended Answer,
Affirmative Defenses, and Counterclaims to add various antitrust counterclaims
resulting from the injunction that was issued against DRL. The motion was
granted in November 2019. In January 2020, Indivior and DRL entered into a
joint stipulation that DRL did not infringe the '305 Patent based on the
District Court's claim construction ruling, but that Indivior retained its
right to appeal the issue of infringement of the '305 Patent. Indivior
maintains its infringement claims on the '454 patent, and DRL maintains its
counterclaims. No trial date has been set for either the patent claims or the
antitrust counterclaims.
· In November 2018, DRL filed two separate petitions for inter
partes review ("IPR") of the '454 Patent with the USPTO. The USPTO denied
institution of one of the IPR petitions but granted institution for the second
IPR petition. The Patent Trial and Appeal Board (USPTO) issued a decision in
June 2020, holding that claims 1-5, 7, and 9-14 were unpatentable, but that
DRL had not shown that claim 8 is unpatentable. Claim 6 was not challenged and
therefore was not addressed in the PTAB decision. Indivior appealed to the
Court of Appeals for the Federal Circuit in July 2020. No court date has been
set yet.
· Litigation against Alvogen is pending in the United States
District Court for the District of New Jersey regarding the '454 and '305
Patents. In January 2019, Indivior filed a motion for a temporary restraining
order ("TRO") and preliminary injunction in the District of New Jersey,
requesting that the Court restrain the launch of Alvogen's generic
buprenorphine/naloxone film product until a trial on the merits of the '305
Patent. Alvogen received approval for its generic product in January 2019. The
same day, the District of New Jersey granted a TRO until February 7, 2019. In
January 2019, Indivior and Alvogen entered in to an agreement whereby Alvogen
was enjoined from the use, offer to sell, or sale within the United States, or
importation into the United States, of its generic buprenorphine and naloxone
sublingual film product unless and until the CAFC issued a mandate vacating
the PI against DRL. The mandate vacating the DRL PI issued in February 2019,
and Alvogen launched its generic product. Any sales in the US are on an
"at-risk" basis, subject to the ongoing litigation against Alvogen in the
District of New Jersey. In August 2019, Alvogen filed a motion for leave to
file an amended Answer to Complaint and Separate Defenses and Counterclaims to
add various antitrust counterclaims. The motion was granted in November 2019.
In January 2020, Indivior and Alvogen entered into a joint stipulation that
Alvogen did not infringe the '305 Patent based on the District Court's claim
construction ruling, but that Indivior retained its right to appeal the issue
of infringement of the '305 Patent. Indivior maintains its infringement claims
on the '454 patent, and Alvogen maintains its counterclaims. No trial date has
been set for either the patent claims or the antitrust counterclaims.
Opposition to SUBLOCADE European Patent
· In October 2018, Teva Pharmaceutical Industries Ltd. ("Teva")
filed a Notice of Opposition with the European Patent Office seeking to revoke
European Patent No. EP 2579874 ("EP 874"), which relates to the formulation
for SUBLOCADE. Oral proceedings are scheduled to take place in September 2021.
· In March 2021, the law firm Elkington & Fife LLP filed a
Notice of Opposition with the European Patent Office seeking to revoke
European Patent No. EP 3215223 ("EP 223"), which relates to the dosing regimen
for SUBLOCADE. The Opposition alleges that the claims of EP 223 lack inventive
step and extend beyond the content of the application as originally filed. The
Group will respond to the Opposition on or before the deadline in August 2021.
Antitrust Litigation and Consumer Protection
Antitrust Class and State Claims
· Civil antitrust claims have been filed by (a) a class of direct
purchasers, (b) a class of end payor plaintiffs, and (c) a group of states,
now numbering 41, and the District of Columbia. Each set of plaintiffs filed
generally similar claims alleging, among other things, that Indivior violated
U.S. federal and/or state antitrust and consumer protection laws in attempting
to delay generic entry of alternatives to SUBOXONE Tablets. Plaintiffs further
allege that Indivior unlawfully acted to lower the market share of these
products. These antitrust cases are pending in federal court in the Eastern
District of Pennsylvania. The court has not set a trial date. Summary judgment
motions related to the Direct Purchaser, End Payor, and States actions were
filed in March 2021. Opposition briefs were filed in April 2021 and reply
briefs are due in May 2021.
· In 2013, Reckitt Benckiser Pharmaceuticals, Inc. (now known as
Indivior Inc.) received notice that it and other companies were defendants in
a lawsuit initiated by writ in the Philadelphia County (Pennsylvania) Court of
Common Pleas. See Carefirst of Maryland, Inc. et al. v. Reckitt Benckiser
Inc., et al., Case. No. 2875, December Term 2013. The plaintiffs include
approximately 79 entities, most of which appear to be insurance companies or
other providers of health benefits plans. The Carefirst Plaintiffs have not
served a complaint, but they have indicated that their claims are related to
those asserted by the plaintiffs in re Suboxone, MDL No. 2445 (E.D. Pa.). In
February 2021, the Court sent a Notice of Proposed Termination. The Carefirst
case remains pending.
The Group has evaluated the antitrust class and state claims in light of the
DOJ settlement under which a Group subsidiary plead guilty to one count of
making a false statement relating to health care matters in one state in 2012.
The Group continues to believe in its defenses and continues to vigorously
defend itself. Select plaintiffs in these matters have previously made
settlement demands (which were not accepted and most of which are not current
offers), totaling approximately $290m, which was used for contingency planning
only to model possible downside financial effects. The final aggregate cost of
these matters, whether resolved by litigation or by settlement, may be
materially different. If the Group were to entertain further settlement
discussions, we make no representations as to what amounts, if any, it may
agree to pay, nor regarding what amounts the plaintiffs will demand.
Other Antitrust and Consumer Protection Claims
· In July 2019, the Indiana Attorney General issued a Civil
Investigative Demand investigating potential violations of Indiana's Civil
Deceptive Consumer Sales Act with respect to sales and marketing activity by
the Company. The Group is cooperating fully in this civil investigation.
· In 2020, the Group was served with lawsuits from a number of
insurance companies, some of whom are proceeding both on their own claims and
through the assignment of claims from affiliated companies. Cases filed by (1)
Humana Inc. and (2) Centene Corporation, Wellcare Healthcare Plans, Inc., New
York Quality Healthcare Corp. (d/b/a Fidelis Care), and Health Net, LLC are
pending in the Eastern District of Pennsylvania. Cases filed by (1) Blue Cross
and Blue Shield of Massachusetts, Inc., Blue Cross and Blue Shield of
Massachusetts HMO Blue, Inc., (2) Health Care Service Corp., (3) Blue Cross
and Blue Shield of Florida, Inc., Health Options, Inc., (4) BCBSM, Inc. (d/b/a
Blue Cross and Blue Shield of Minnesota) and HMO Minnesota (d/b/a Blue Plus),
and (5) Molina Healthcare, Inc. are pending in the Circuit Court for the
County of Roanoke, Virginia. The allegations in these cases include many
allegations made in other litigations, including prior antitrust complaints,
indictments, and qui tam complaints. These plaintiffs have asserted claims
under federal and state RICO statutes, state antitrust statutes, state
statutes prohibiting unfair and deceptive practices, state statutes
prohibiting insurance fraud, and common law fraud, negligent
misrepresentation, and unjust enrichment. Defendants' motions to dismiss are
fully briefed and pending.
The Group has begun its preliminary evaluation of the claims, believes in its
defenses, and intends to vigorously defend itself. Currently, engagement with
the claimants has been minimal and the Group's evaluation of the various
claims is in preliminary stages. Accordingly, no estimate of the range of
potential loss can be made at this time.
Civil Opioid Litigation
· Indivior has been named as a defendant in fewer than 400 civil
lawsuits brought by state and local governments, public health agencies, and
individuals against manufacturers, distributors and retailers of opioids
alleging that they engaged in a longstanding practice to market opioids as
safe and effective for the treatment of long term chronic pain in order to
increase the market for opioids and their own market share. The vast majority
of these cases have been consolidated and are pending in a federal
multi-district litigation (MDL) in U.S. District Court for the Northern
District of Ohio. At the present time, litigation against Indivior in the MDL
is stayed. There remain three (3) cases against Indivior pending in state
courts located in Arizona, Pennsylvania and Virginia, which are similarly
stayed at the current time. Given the status and preliminary stage of
litigation in both the MDL and state courts, no estimate of possible loss in
the opioid litigation can be made at this time.
12. TRADE AND OTHER PAYABLES
Mar 31 Dec 31
2021 2020
$m $m
Sales returns and rebates (408) (396)
Trade payables (25) (20)
Accruals (85) (99)
Other tax and social security payables (11) (9)
Total (529) (524)
Sales return and rebate accruals, primarily in the U.S., are provided in
respect of the estimated rebates, discounts or allowances payable to direct
and indirect customers. Accruals are made at the time of sale while the actual
amounts to be paid are based on claims made some time after the initial
recognition of the sale. As the amounts are estimated, they may not fully
reflect the final outcome and are subject to change dependent upon, amongst
other things, the payor channel (e.g. Medicaid, Medicare, Managed Care, etc.)
and product mix. The level of accrual is reviewed and adjusted in the light of
historical experience of actual rebates, discounts or allowances given and
returns made, and any changes in arrangements or rules. Future events may
cause the assumptions on which the accruals are based to change, which could
affect the future results of the Group.
13. SHARE CAPITAL
Equity ordinary shares Nominal value paid per share Aggregate nominal value
$m
Issued and fully paid
At January 1, 2021 733,635,511 $0.10 73
Allotments 985,478 $0.10 -
At March 31, 2021 734,620,989 73
Equity ordinary shares Nominal value paid per share Aggregate nominal value
$m
Issued and fully paid
At January 1, 2020 730,787,719 $0.10 73
Allotments 1,620,613 $0.10 -
At March 31, 2020 732,408,332 73
Allotment of ordinary shares
During the period, 985,478 ordinary shares (2020: 1,620,613) were allotted to
satisfy vestings/exercises under the Group's Long-Term Incentive Plan and U.S.
Employee Stock Purchase Plan.
14. POST BALANCE SHEET EVENTS
On April 12, 2021 the Internal Revenue Service approved a tax credit in
relation to development credits for SUBLOCADE claimed in prior years and
issued a refund for approximately $36m. The Group accounted for this event as
an adjusting post balance sheet event. See Notes 3 and 5 for further
discussion.
DIRECTORS' RESPONSIBILITY STATEMENT
The Directors declare that, to the best of their knowledge:
· This set of Condensed Consolidated Interim Financial Statements,
which have been prepared in accordance with International account standard 34,
'Interim Financial Reporting', as contained in UK-adopted international
accounting standards ("IAS 34"), gives a true and fair view of the assets,
liabilities, financial position, and profit or loss of Indivior; and
· The interim management report gives a fair review of the
information in line with regulations 4.2.7 and 4.2.8 of the Disclosure
Guidance and Transparency Rules.
The Directors are responsible for the maintenance and integrity of the Group's
website. Legislation in the United Kingdom governing the preparation and
dissemination of financial statements may differ from legislation in other
jurisdictions.
Indivior PLC's Directors are listed in the Annual Report and Accounts for
2020. Jerome Lande, Jo Le Couilliard, Mark Stejbach and Juliet Thompson were
appointed as Non-Executive Directors on March 23, 2021.
Details of all current Directors are available on our website at
www.indivior.com (http://www.indivior.com)
By order of the Board
Mark
Crossley
Ryan Preblick
Chief Executive
Officer
Chief Financial Officer
April 28, 2021
Independent review report to Indivior PLC
Report on the Condensed consolidated interim financial statements
Our conclusion
We have reviewed Indivior PLC's Condensed consolidated interim financial
statements (the "interim financial statements") in the Q1 2021 Results of
Indivior PLC for the three month period ended 31 March 2021 (the "period").
Based on our review, nothing has come to our attention that causes us to
believe that the interim financial statements are not prepared, in all
material respects, in accordance with International Accounting Standard 34,
'Interim Financial Reporting', as contained in UK-adopted international
accounting standards ("IAS 34").
What we have reviewed
The interim financial statements comprise:
· the Condensed consolidated interim balance sheet as at
31 March 2021;
· the Condensed consolidated interim income statement and Condensed
consolidated interim statement of comprehensive income/(loss) for the period
then ended;
· the Condensed consolidated interim statement of changes in equity
for the period then ended;
· the Condensed consolidated interim cash flow statement for the
period then ended; and
· the explanatory notes to the interim financial statements.
The interim financial statements included in the Q1 2021 Results of Indivior
PLC have been prepared in accordance with IAS 34.
As disclosed in note 1 to the interim financial statements, the financial
reporting framework that will be applied in the preparation of the next full
annual financial statements of the group is applicable law and UK-adopted
international accounting standards.
Responsibilities for the interim financial statements and the review
Our responsibilities and those of the directors
The Q1 2021 Results, including the interim financial statements, is the
responsibility of, and has been approved by the directors. The directors are
responsible for preparing the Q1 2021 Results in accordance with IAS 34.
Our responsibility is to express a conclusion on the interim financial
statements in the Q1 2021 Results based on our review. We do not, in giving
this conclusion, accept or assume responsibility for any other purpose or to
any other person to whom this report is shown or into whose hands it may come
save where expressly agreed by our prior consent in writing.
What a review of interim financial statements involves
We conducted our review in accordance with International Standard on Review
Engagements (UK and Ireland) 2410, 'Review of Interim Financial Information
Performed by the Independent Auditor of the Entity' issued by the Auditing
Practices Board for use in the United Kingdom. A review of interim financial
information consists of making enquiries, primarily of persons responsible for
financial and accounting matters, and applying analytical and other review
procedures.
A review is substantially less in scope than an audit conducted in accordance
with International Standards on Auditing (UK) and, consequently, does not
enable us to obtain assurance that we would become aware of all significant
matters that might be identified in an audit. Accordingly, we do not express
an audit opinion.
We have read the other information contained in the Q1 2021 Results and
considered whether it contains any apparent misstatements or material
inconsistencies with the information in the interim financial
statements.
PricewaterhouseCoopers LLP
Chartered Accountants
London
28 April 2021
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