Biomea Fusion Announces Acceptance of Three Abstracts for its Novel Menin Inhibitor Highlighting Durable Glycemic Control in Diabetes Patients at the International Conference on Advanced Technologies & Treatments for Diabetes (ATTD) in 2024
27 Novembro 2023 - 10:30AM
Biomea Fusion, Inc. (“Biomea”) (Nasdaq: BMEA), a clinical-stage
biopharmaceutical company dedicated to discovering and developing
novel covalent small molecules to treat and improve the lives of
patients with genetically defined cancers and metabolic diseases,
today announced the acceptance of three abstracts presenting new
clinical data from the ongoing escalation portion of its
COVALENT-111 trial, evaluating BMF-219 as a potential treatment for
people with type 2 diabetes, at the 17th International Conference
on Advanced Technologies & Treatments for Diabetes (ATTD)
taking place in Florence, Italy, 6-9 March 2024. This new clinical
data from all dosing cohorts initiated to date from the escalation
portion of COVALENT-111 will be featured during a Poster Discussion
Presentation and two Poster Viewing Presentations at ATTD.
These abstracts further validate the mechanism of action of
covalently inhibiting menin in people with type 2 diabetes to
potentially provide long-term improvement in glycemic control
through beta cell regeneration.
Biomea will disclose additional information about the
presentations in accordance with the ATTD abstract embargo
policies.
Accepted 2024 ATTD Abstract Titles
- Abstract Submission
Number: 101 Presentation
Session: E-Poster Discussion SessionAbstract
Title: Durable Glycemic Control with BMF-219 during
off-Treatment Period at Week 26: a Phase 1/2 Trial of BMF-219 in
Patients with Type 2 Diabetes (COVALENT-111)
- Abstract Submission
Number: 751Presentation Session:
E-Poster Viewing Session Abstract
Title: Key Observations from the Dose – Escalation
Portion of COVALENT-111, a Phase 1/2 Trial of the Covalent Menin
Inhibitor BMF-219 in Patients with Type 2 Diabetes
- Abstract Submission
Number: 722 Presentation
Session: E-Poster Viewing Session Abstract
Title: Case Studies from COVALENT-111, a Phase 1/2
Trial of BMF-219, a Covalent Menin Inhibitor, in Patients with Type
2 Diabetes
COVALENT-111
COVALENT-111 is a multi-site, randomized, double-blind,
placebo-controlled Phase I/II study. In the completed Phase I
portion of the trial, healthy subjects were enrolled in single
ascending dose cohorts to ensure safety at the prospective dosing
levels for people with type 2 diabetes. Phase II consists of
multiple ascending dose cohorts and dose durations and includes
adult patients with type 2 diabetes uncontrolled by current
therapies. Additional information about the Phase I/II clinical
trial of BMF-219 in type 2 diabetes can be found at
ClinicalTrials.gov using the identifier NCT05731544.
About Menin’s Role in Diabetes
Loss of functional beta cell mass is a core component of the
natural history in both types of diabetes — type 1 diabetes
(mediated by autoimmune dysfunction) and type 2 diabetes (mediated
by metabolic dysfunction). Beta cells are found in the pancreas and
are responsible for the synthesis and secretion of insulin. Insulin
is a hormone that helps the body use glucose for energy and helps
control blood glucose levels. In patients with diabetes, beta cell
mass and function have been observed to be diminished, leading to
insufficient insulin secretion and hyperglycemia. Menin is thought
to act as a brake on beta-cell turnover and growth, supporting the
notion that inhibition of menin could lead to the regeneration of
normal, healthy beta cells. Based on these and other scientific
findings, Biomea is exploring the potential for BMF-219-mediated
menin inhibition as a viable therapeutic approach to potentially
halt or reverse progression of type 2 diabetes.
About Type 2 Diabetes
Diabetes is considered a chronic health condition that affects
how the body turns food into energy and results in too much sugar
in the bloodstream. Over time, this can cause serious health
problems and damage vital organs. Most people with diabetes have a
shorter life expectancy than people without this disease. The CDC
estimates about 2 in 5 of the adult population in the USA are now
expected to develop diabetes during their lifetime. More than 37
million people of all ages (about 11% of the US population) have
diabetes today. 96 million adults (more than 1 in 3) have
pre-diabetes, blood sugars that are higher than normal but not high
enough to be classified as diabetes. Diabetes is also one of the
largest economic burdens on the United States health care system
with $1 out of every $4 in US health care costs being spent on
caring for people with diabetes. Despite the current availability
of many diabetes medications, there remains a significant need in
the treatment and care of patients with diabetes.
About Biomea Fusion
Biomea Fusion is a clinical stage biopharmaceutical company
focused on the discovery and development of covalent small
molecules to treat patients with genetically defined cancers and
metabolic diseases. A covalent small molecule is a synthetic
compound that forms a permanent bond to its target protein and
offers a number of potential advantages over conventional
non-covalent drugs, including greater target selectivity, lower
drug exposure, and the ability to drive a deeper, more durable
response. We are utilizing our proprietary FUSION™ System to
discover, design and develop a pipeline of next-generation
covalent-binding small molecule medicines designed to maximize
clinical benefit for patients with various cancers and metabolic
diseases, including diabetes. We aim to have an outsized impact on
the treatment of disease for the patients we serve. We aim to
cure.
Visit us at biomeafusion.com and follow us on LinkedIn, Twitter
and Facebook.
Forward-Looking Statements
Statements we make in this press release may include statements
which are not historical facts and are considered forward-looking
statements within the meaning of Section 27A of the Securities Act
of 1933, as amended (the “Securities Act”), and Section 21E of the
Securities Exchange Act of 1934, as amended (the “Exchange Act”).
These statements may be identified by words such as “aims,”
“anticipates,” “believes,” “could,” “estimates,” “expects,”
“forecasts,” “goal,” “intends,” “may,” “plans,” “possible,”
“potential,” “seeks,” “will,” and variations of these words or
similar expressions that are intended to identify forward-looking
statements. Any such statements in this press release that are not
statements of historical fact, including statements regarding the
clinical and therapeutic potential of our product candidates and
development programs, including BMF-219, the potential of BMF-219
as a treatment for diabetes, our research, development and
regulatory plans, including our pursuit of BMF-219 in metabolic
diseases, our plans to continue the evaluation of BMF-219 for type
2 diabetes in our COVALENT-111 study, that initial results may not
be indicative of final results in later clinical trials, the
availability of future data from the Phase II portion of the study,
and the timing of such events, may be deemed to be forward-looking
statements. We intend these forward-looking statements to be
covered by the safe harbor provisions for forward-looking
statements contained in Section 27A of the Securities Act and
Section 21E of the Exchange Act and are making this statement for
purposes of complying with those safe harbor provisions.
Any forward-looking statements in this press release are based
on our current expectations, estimates and projections only as of
the date of this release and are subject to a number of risks and
uncertainties that could cause actual results to differ materially
and adversely from those set forth in or implied by such
forward-looking statements, including the risk that we may
encounter delays or unforeseen results in preclinical development,
IND-filing and acceptance, patient enrollment and in the
initiation, conduct and completion of our planned clinical trials
and other research, development and regulatory activities. These
risks concerning Biomea Fusion’s business and operations are
described in additional detail in its periodic filings with the
U.S. Securities and Exchange Commission (the “SEC”), including its
most recent periodic report filed with the SEC and subsequent
filings thereafter. Biomea Fusion explicitly disclaims any
obligation to update any forward-looking statements except to the
extent required by law.
Contact:
Investor Relations
Chunyi Zhao, PhD
Sr. Manager of Investor Relations & Corporate Development
czhao@biomeafusion.com
Media Relations
Neera Chaudhary, PhD
Chief Commercial Officer – Diabetes
nchaudhary@biomeafusion.com
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