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Arix Bioscience PLC (ARIX)
Portfolio Company Imara Announces Merger Agreement with Enliven
Therapeutics
14-Oct-2022 / 07:00 GMT/BST
Dissemination of a Regulatory Announcement, transmitted by EQS Group.
The issuer is solely responsible for the content of this announcement.
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Arix Bioscience plc
Portfolio Company Imara Announces Merger Agreement with Enliven
Therapeutics
Merger to create a Nasdaq-listed, clinical-stage biopharmaceutical company
focused on advancing Enliven’s pipeline of precision oncology product
candidates
Transaction to concurrently raise approximately $165 million in a private
financing co-led by new investors Fairmount and Venrock Healthcare Capital
Partners, with participation from additional new investors
LONDON, 14 October 2022: Arix Bioscience plc (LSE: ARIX), a global venture
capital company focused on investing in breakthrough biotechnology
companies, notes that its portfolio company, Imara Inc. (“Imara”) (Nasdaq:
IMRA), has entered into a definitive merger agreement with Enliven
Therapeutics, Inc. (“Enliven”) to create a Nasdaq-listed clinical-stage
biopharmaceutical company in an all-stock transaction. The combined
company will focus on advancing Enliven’s pipeline of precision oncology
product candidates. Upon shareholder approval, the combined company is
expected to operate under the name Enliven Therapeutics, Inc. and trade on
the Nasdaq Global Select Market under the ticker symbol ELVN.
In support of the merger, Enliven also intends to raise approximately $165
million in a concurrent private financing co-led by new investors
Fairmount and Venrock Healthcare Capital Partners, with participation from
additional new investors, which include Fidelity Management & Research
Company, RA Capital Management, Frazier Life Sciences and Commodore
Capital. With the cash expected from both companies at closing and the
proceeds of the planned concurrent financing, the combined company is
currently expected to have approximately $300 million of cash and cash
equivalents at closing, after transaction expenses. The cash resources are
expected to be used to advance Enliven’s pipeline through multiple
clinical milestones and provide runway into early 2026.
Robert Lyne, CEO of Arix Bioscience, stated: “The merger of Enliven with
Imara will bring a differentiated, clinical stage pipeline of precision
oncology assets to the public market. We are pleased to note that with the
proposed financing backed by a group of top tier investors, the combined
company will be well funded with sufficient cash to achieve multiple
clinical development milestones into 2026.”
ENDS
For more information on Arix, please contact:
Arix Bioscience plc
+44 (0)20 7290 1050
1 ir@arixbioscience.com
Powerscourt Group
Sarah MacLeod, Ibrahim Khalil, Nick Johnson
+44 (0)20 7250 1446
Notes to Editors
About Enliven Therapeutics, Inc.
Enliven Therapeutics is a clinical-stage biopharmaceutical company focused
on the discovery and development of small molecule inhibitors to help
patients with cancer live not only longer, but better. Enliven aims to
address existing and emerging unmet needs with a precision oncology
approach that improves survival and enhances overall patient well-being.
Enliven’s discovery process combines deep insights from clinically
validated biological targets and differentiated chemistry to design
potentially first-in-class or best-in-class therapies. Enliven is based in
Boulder, Colorado.
About Enliven’s Precision Oncology Portfolio
Enliven is a clinical-stage precision oncology company focused on the
discovery and development of potentially best-in-class or first-in-class
precision oncology therapies. Enliven’s programs are designed to address
issues such as tolerability, combinability, resistance and disease escape
through brain metastases. Enliven is advancing two parallel lead product
candidates:
ELVN-001: Enliven’s most advanced candidate, ELVN-001, is a potent, highly
selective, small molecule kinase inhibitor designed to specifically target
the BCR-ABL gene fusion, the oncogenic driver for patients with CML.
Although the approval of BCR-ABL TKIs has improved the life expectancy of
patients with CML significantly, tolerability, safety, resistance and
patient convenience concerns have become more prominent as patients can
now expect to live on therapy for decades. These issues can result in the
loss of molecular response and disease progression for many patients and
drive approximately 20% of patients to switch therapy within the first
year and approximately 40% to switch in the first 5 years. Enliven’s
preclinical studies showed that ELVN-001 does not meaningfully interfere
with the activity of kinases that we believe limit efficacy and
tolerability of approved ATP-competitive TKIs. Additionally, given
ELVN-001's mechanism of action, it potentially represents a complementary
option to allosteric BCR-ABL inhibitors, which may play an increasingly
important role in the standard of care. ELVN-001 was also designed to be
efficacious against the T315I mutation, the most common BCR-ABL mutation,
which confers resistance to nearly all approved TKIs. Importantly,
ELVN-001 was designed to be a more attractive option for patients with
comorbidities, on concomitant medications or desiring more freedom from
stringent administration requirements. ELVN-001 is currently being
evaluated in a Phase 1 clinical
trial in adults with CML. To learn more, please visit
www.clinicaltrials.gov (NCT05304377).
ELVN-002: Enliven’s second product candidate, ELVN-002, is a potent,
selective and irreversible HER2 inhibitor with activity against various
HER2 mutations, including Exon 20 insertion mutations (E20IMs) in
non-small cell lung cancer (NSCLC), for which there are currently no
approved small molecule inhibitors. ELVN-002 is designed to inhibit HER2
and key mutations of HER2, while sparing wild-type EGFR and avoiding
EGFR-related toxicities. Enliven believes that if ELVN-002 achieves this
profile, it will be able to achieve an improved therapeutic index compared
to current approved and investigational TKIs as well as provide a
meaningful therapeutic option to patients with brain metastases, a key
mechanism of resistance to current therapies in patients with NSCLC and
other HER2 driven diseases. While the initial focus for this program is
for HER2 mutant NSCLC, Enliven intends to seek to expand the opportunity
to patients with other HER2 mutations as well as HER2 amplified tumors
including breast, colorectal, and gastric cancers.
In addition to its two lead programs, Enliven is pursuing several
additional research stage opportunities that align with its development
approach. Enliven is in the process of screening and optimizing the
chemistry for multiple programs and expects to make a product candidate
nomination for its third program in the first half of 2023.
About Arix Bioscience plc
Arix Bioscience plc is a global venture capital company focused on
investing in breakthrough biotechnology companies around cutting-edge
advances in life sciences.
We collaborate with exceptional entrepreneurs and provide the capital,
expertise, and global networks to help accelerate their ideas into
important new treatments for patients. As a listed company, we are able to
bring this exciting growth phase of our industry to a broader range of
investors. 2 www.arixbioscience.com
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ISIN: GB00BD045071
Category Code: PFU
TIDM: ARIX
LEI Code: 213800OVT3AHQCXNIX43
OAM Categories: 3.1. Additional regulated information required to be
disclosed under the laws of a Member State
Sequence No.: 194477
EQS News ID: 1463613
End of Announcement EQS News Service
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