============
Arix Bioscience PLC (ARIX)
Portfolio Company Disc Medicine Enters Definitive Merger Agreement with
Gemini Therapeutics
10-Aug-2022 / 17:46 GMT/BST
Dissemination of a Regulatory Announcement, transmitted by EQS Group.
The issuer is solely responsible for the content of this announcement.
══════════════════════════════════════════════════════════════════════════
Arix Bioscience plc
Portfolio Company Disc Medicine Enters Definitive Merger Agreement with
Gemini Therapeutics
Merger to create a Nasdaq-listed, clinical stage biopharmaceutical company
focused on advancing Disc Medicine’s portfolio of haematology programmes
Transaction will fund multiple clinical studies, including clinical trials
of bitopertin for erythropoietic porphyrias, DISC-0974 for anaemia of
myelofibrosis, and DISC-0974 for anaemia of chronic kidney disease
LONDON, 10 August 2022: Arix Bioscience plc (LSE: ARIX), a global venture
capital company focused on investing in breakthrough biotechnology
companies, notes that its portfolio company, Disc Medicine, Inc. (“Disc”),
has entered into a definitive merger agreement with Gemini Therapeutics,
Inc. (Nasdaq: GMTX) (“Gemini”) to create a Nasdaq-listed clinical-stage
biopharmaceutical company in an all-stock transaction. The combined
company will focus on advancing Disc’s pipeline of haematology programmes,
including multiple patient studies for its clinical stage programmes. Upon
shareholder approval, the combined company is expected to operate under
the name Disc Medicine, Inc, and trade on the Nasdaq Global Market under
the ticker symbol IRON.
In support of the merger, Arix will participate in a $53.5 million
financing in a syndicate of healthcare investors led by Access
Biotechnology and including OrbiMed, Atlas Venture, 5AM Ventures, Novo
Holdings A/S, Rock Springs Capital and Janus Henderson Investors. With the
cash expected from both companies at closing and the proceeds of the
concurrent financing, the combined company is expected to have
approximately $175 million of cash or cash equivalents, which will be used
to advance Disc’s pipeline through multiple clinical studies and provide
runway into 2025. The merger and related financing are expected to close
in the fourth quarter of 2022.
Disc also announced the initiation of BEACON, a Phase 2 clinical study of
bitopertin in patients with Erythropoietic Protoporphyria (EPP) or
X-linked Protoporphyria (XLP). Bitopertin is an oral, selective inhibitor
of glycine transporter 1 (GlyT1) designed to modulate heme biosynthesis
and has been shown in preclinical studies to reduce accumulation of
protoporphyrin in IX (PPIX), the toxic metabolite that causes disease
pathology in EPP and XLP patients.
Robert Lyne, CEO of Arix Bioscience, stated: “The merger with Gemini
represents an exciting opportunity for Disc Medicine. Led by a highly
credible management team, Disc has built a diversified, clinical stage
pipeline of products focused on diseases of unmet medical need. In less
than one year since our initial investment, Disc has made rapid clinical
progress, advancing two programmes into patient studies in the past few
months. Today’s announcement of the merger agreement follows a thorough
and thoughtful strategic review process by Gemini and is validation of our
refocused strategy to invest in companies with nearer-term value
inflection points.”
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 Gemini Therapeutics, Inc.
Gemini Therapeutics is a clinical-stage precision medicine company
previously focused on developing novel therapeutic compounds to treat
genetically defined age-related macular degeneration (AMD).
For more information, visit www.geminitherapeutics.com.
About Disc Medicine, Inc.
Disc Medicine is a clinical-stage biopharmaceutical company that is
dedicated to transforming the lives of patients with hematologic
disorders. Disc is building a portfolio of innovative, first-in-class
therapeutic candidates that affect fundamental pathways of red blood cell
biology. Disc Medicine is committed to developing treatments that empower
and bring hope to the many patients who suffer from hematologic disease.
For more information, please visit www.discmedicine.com.
About Disc Medicine’s Haematology Portfolio
Disc has a clinical-stage development pipeline composed of investigational
product candidates that affect heme biosynthesis and iron metabolism.
Disc’s programs are designed to target pathways with established,
clinically-validated biology and have the potential to address multiple
indications. This includes:
Bitopertin (Heme Synthesis Modulator): Bitopertin is an inhibitor of
glycine transporter, GlyT1, and has demonstrated effects on heme
biosynthesis in clinical studies. Bitopertin was in-licensed by Disc from
Roche in 2021 and has been extensively studied, including a safety data
package reflecting clinical experience in over 4,000 individuals.
Inhibition of heme biosynthesis has the potential to address a wide range
of hematologic disorders. Disc has initiated BEACON, an open-label, phase
2 trial of bitopertin in patients with erythropoietic porphyria, a rare,
debilitating and potentially fatal genetic disorder that results in
dysregulated heme biosynthesis and where bitopertin has the potential to
become the first disease-modifying treatment. Additional clinical studies
in Diamond-Blackfan Anemia (DBA) and other indications are being planned.
DISC-0974 (Hepcidin Suppression): DISC-0974 is a monoclonal antibody
targeting a co-receptor called hemojuvelin (HJV) and is designed to
suppress hepcidin production and increase serum iron levels in patients
suffering from the anemia of inflammation. DISC-0974 was in-licensed by
Disc from AbbVie in 2019. Anemia of inflammation arises from abnormally
elevated hepcidin and is the most common form of anemia, affecting
millions of patients across numerous diseases such as chronic kidney
disease, myelofibrosis, cancer, autoimmune diseases, and other conditions
with an inflammatory component. Disc has established clinical
proof-of-mechanism of DISC-0974 in a phase 1 study of healthy volunteers
and initiated a phase 1b/2 clinical study of DISC-0974 in patients with
anemia of myelofibrosis. Disc plans to initiate a phase 1b/2 clinical
study of DISC-0974 in patients with anemia of chronic kidney disease
(non-dialysis) in late 2022.
Matriptase-2 Inhibitor (Hepcidin Induction): Disc has a research program
designed to identify orally-available, small molecules to inhibit
Matriptase-2 (referred to as Mat-2 or TMPRSS6) and increase the production
of hepcidin and restrict iron availability. The therapeutic role of
hepcidin has been established in patients with polycythemia vera and
hereditary hemochromatosis, and is being studied for the treatment of
diseases associated with iron overload, including beta-thalassemia,
myelodysplastic syndromes, and sickle cell disease.
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
══════════════════════════════════════════════════════════════════════════
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.: 180589
EQS News ID: 1417989
End of Announcement EQS News Service
══════════════════════════════════════════════════════════════════════════
3 fncls.ssp?fn=show_t_gif&application_id=1417989&application_name=news&site_id=reuters9
References
Visible links
1. mailto:ir@arixbioscience.com
2. https://eqs-cockpit.com/cgi-bin/fncls.ssp?fn=redirect&url=889c637ce21c3a47a35c39202ebd9825&application_id=1417989&site_id=reuters9&application_name=news
============