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 metabolic diseases, obesity and genetically defined
cancers, today announced the formation of Biomea Fusion’s Global
Scientific Advisory Board (SAB) with internationally renowned
experts in beta cell science and diabetes therapeutics. The SAB
will work closely with Biomea’s leadership team as they unlock
menin science and beta cell biology to design disease modifying
agents that address a root cause of diabetes – beta cell
dysfunction. The SAB will also provide strategic guidance for the
further clinical development of Biomea’s lead candidate BMF-219 –
an investigational novel covalent menin inhibitor developed to
regenerate, restore, and improve the health and function of
insulin-producing beta cells.
“We are excited to welcome these extraordinary
and prestigious scientific leaders to the Biomea Scientific
Advisory Board,” said Thomas Butler, CEO and Chairman of Biomea.
“Each of these visionaries has made groundbreaking contributions to
diabetes therapeutics and beta cell research. Together, they form a
powerhouse of expertise and innovation for Biomea, which will be
invaluable as we leverage our deep understanding of menin science
to regenerate insulin-producing beta cells."
Juan Pablo Frias, Chief Medical Officer and Head
of Diabetes at Biomea said, “We are honored to convene a
world-class SAB, that represents remarkable experience and
knowledge across diabetes drug development, data-driven global
clinical trial design, and beta cell biology. With our advisors’
leadership, expertise and collaboration, we will optimize our
clinical development and commercialization path for BMF-219."
“I’ve had the privilege of collaborating with
Biomea since mid-2022, witnessing firsthand the groundbreaking
FUSION platform poised to revolutionize beta cell science and the
diabetes space,” said Rohit N. Kulkarni, M.D. Ph.D, Chair of
Biomea’s SAB. “I am excited to lead this effort for Biomea and
welcome this group of world-renowned leaders to Biomea's SAB at
this crucial juncture in the company’s evolution. Together, we will
start with taking a deep dive into the clinical data generated to
date with BMF-219 and review the overall path towards
commerciality. We will explore the potential for BMF-219 as a
monotherapy as well as in combination with standard of care agents
and provide our advice to the clinical and scientific team at the
company. We look forward to further unlock the immense potential of
menin science and islet cell biology.”
The inaugural members of the Global Biomea SAB are listed below.
Full biographies of SAB members can be found at
https://biomeafusion.com/leadership/.
Alex Abitbol, MD, is an
accomplished endocrinologist and Assistant Medical Director at LMC
Healthcare in Toronto, Ontario. He completed his medical education
and specialized in Endocrinology and Metabolism at McGill
University. Dr. Abitbol focuses on diabetes care and management,
particularly applying technology to improve patient outcomes,
including developing the artificial pancreas and automated insulin
therapy. He is a principal investigator at Centricity Research,
involved in clinical trials for diabetes and cardiovascular
disease. Board-certified in Internal Medicine and Endocrinology,
Dr. Abitbol frequently speaks at conferences and is dedicated to
advancing diabetes management technologies and patient care.
Pablo Aschner Montoya, MD is an
endocrinologist and diabetes researcher, serving as an Associate
Professor of Endocrinology at Javeriana University School of
Medicine in Bogotá, Colombia. He is also the Senior Research
Advisor at San Ignacio University Hospital and the Scientific
Director of the Colombian Diabetes Association. Dr. Aschner holds a
medical degree from Javeriana University, specialized in internal
medicine and endocrinology, and obtained a master’s in clinical
Epidemiology. His research focuses on the prevention, diagnosis,
control, and treatment of diabetes, emphasizing type 2 diabetes and
its complications has significantly contributed to understanding
diabetes care practices through influential studies like the
International Diabetes Management Practices Study (IDMPS). He has
held leadership roles in the Colombian Endocrine Society and the
Latin American Diabetes Association (ALAD) and has been a member of
the WHO Expert Advisory Panel and the IDF taskforce on
Guidelines.
Juliana Chan, MD is an
endocrinologist, clinical pharmacologist and a diabetes researcher,
currently serving as a Professor of Medicine and Therapeutics at
The Chinese University of Hong Kong (CUHK). She is the Founding
Director of the Hong Kong Institute of Diabetes and Obesity and the
CEO of the Asia Diabetes Foundation. Dr. Chan also directs the
CUHK-PWH International Diabetes Federation (IDF) Centre of
Education and Centre of Excellence in Diabetes Care. Dr. Chan's
research focuses on the epidemiology, genetics, clinical trials and
data-driven clinical management of diabetes. She established the
Hong Kong Diabetes Register and developed the Joint Asia Diabetes
Evaluation (JADE) Technology, a web-based platform used in 11 Asian
countries. This innovative approach has enrolled over 120,000
patients with diabetes and significantly contributed to a decline
in the death rate among people with diabetes in Hong Kong.
Alice YY Cheng, MD is an
endocrinologist and Associate Professor at the University of
Toronto, specializing in endocrinology and metabolism at Trillium
Health Partners and Unity Health Toronto. She completed her medical
education at the University of Toronto in 1998 and has since become
a leading expert in diabetes care. Dr. Cheng has been involved with
the development of the Diabetes Canada clinical practice guidelines
since 2003, serving as Chair for the 2013 version. She is
past-Chair of the Professional Section of Diabetes Canada. Her
contributions have earned her prestigious awards, including the
Charles H. Best Award and the Gerald S. Wong Service Award from
Diabetes Canada. In addition to her clinical work, Dr. Cheng served
as the Chair of the Scientific Planning Committee for the American
Diabetes Association (ADA) annual scientific sessions (2023-2024)
and is an Associate Editor for the journal, Diabetes Care, and
co-hosts the "Diabetes Care On-Air" podcast.
Melanie Davies, MD,
CBE, MB ChB, MD, FRCP, FRCGP, FMedSci is a highly esteemed
endocrinologist and Professor of Diabetes Medicine at the
University of Leicester. She directs the NIHR Leicester Biomedical
Research Centre and the Patient Recruitment Centre Leicester. With
over 25 years in diabetes research and clinical care, she has led
numerous global clinical trials on diabetes, obesity, physical
activity, and cardiovascular disease. Dr. Davies has published over
900 articles, significantly impacting international clinical
guidelines for insulin and GLP-1 therapy. Her co-leadership at the
Leicester Diabetes Centre has established it as a global leader in
diabetes research and education. Honored as a Commander of the
Order of the British Empire (CBE) and elected Fellow of the Academy
of Medical Sciences (FMedSci), Dr. Davies is recognized among the
top 100 female scientists in the UK.
Asma Deeb, MD, MBBS is a highly
respected Consultant and Chief of Pediatric Endocrinology at Sheikh
Shakhbout Medical City (SSMC) in Abu Dhabi, UAE. She is also a
clinical professor at Khalifa University and Gulf University. Dr.
Deeb trained in the UK, obtaining her MD from the University of
Newcastle and specializing in Pediatric Endocrinology at the
University of Cambridge. Her research focuses on disorders of
sexual differentiation, pediatric diabetes management technology,
and diabetes genetics. She has published extensively and conducted
significant studies on diabetes treatments and the effects of
fasting during Ramadan on young diabetes patients. Dr. Deeb is the
President of the Arab Society of Pediatric Endocrinology and
Diabetes (ASPED) and has held leadership roles in several
international pediatric endocrinology organizations. Her
contributions have earned her numerous awards, including the
Research Innovation Award from the Dubai Health Authority and the
Technology Innovation Pioneer award from SEHA.
Ralph A. DeFronzo, MD is a
renowned endocrinologist and diabetes researcher, currently serving
as Professor of Medicine and Chief of the Diabetes Division at the
University of Texas Health Science Center at San Antonio (UTHSCSA)
and Deputy Director of the Texas Diabetes Institute. He graduated
from Yale University and earned his medical degree from Harvard
Medical School, with further training in Internal Medicine at Johns
Hopkins Hospital and fellowships in Endocrinology and Nephrology.
Dr. DeFronzo focuses on the pathogenesis and treatment of type 2
diabetes, particularly insulin resistance. He pioneered the
euglycemic insulin clamp technique and played a key role in
developing and obtaining FDA approval for metformin and SGLT2
inhibitors. He has received numerous prestigious awards, including
the Banting Award and Claude Bernard Award, and published over 800
articles. His contributions have profoundly impacted diabetes
understanding and management, influencing guidelines such as the
ADA's 2022 Standards of Care.
Thomas Danne, MD is a leading
pediatric endocrinologist and diabetes expert who currently serves
as the Chief Medical Officer International for JDRF (formerly JDRF)
and as a Professor of Pediatrics at Hannover Medical School in
Germany. He received his MD from the Medical School of the Freie
University of Berlin and further enhanced his expertise through a
Postdoctoral Fellowship at the German Research Council and a
research fellowship at Harvard's Joslin Research Laboratory. He has
held leadership roles in prominent organizations such as the
International Society for Pediatric and Adolescent Diabetes
(ISPAD), the German Diabetes Association, and INNODIA. With over
700 publications and more than 19,000 citations, Dr. Danne has made
a substantial impact on the field, leading the EDITION JUNIOR
clinical trials and co-authoring the International Consensus on
Time in Range. His innovative approaches, including color-coded
charts for children, have improved diabetes care and management.
Dr. Danne's significant contributions to diabetes research and care
have earned him numerous accolades, including ISPAD Prizes for
Innovation and Achievement, the Helmut-Otto Medal, and a Lifetime
Achievement Award from the International Diabetes Federation.
Linda DiMeglio, MD, MPH is a
celebrated pediatric endocrinologist and expert in type 1 diabetes
research. She is the Edwin Letzter Professor of Pediatrics at
Indiana University School of Medicine, Division Chief of Pediatric
Endocrinology and Diabetology at Riley Children's Health in
Indianapolis, and the co-director of Workforce Development for the
Indiana Clinical and Translational Sciences Institute. Dr. DiMeglio
graduated with honors from Harvard University and obtained her
medical degree from the University of Pennsylvania. She completed
her residency at Children's Memorial Hospital (now Lurie
Children’s) and a fellowship in pediatric endocrinology at Indiana
University-Purdue University, Indianapolis, where she also earned a
Master of Public Health degree. Her research focuses on type 1
diabetes prevention, beta-cell preservation, and new diabetes
management technologies and therapeutics. Dr. DiMeglio has led
numerous clinical trials contributing significantly to the
understanding of beta-cell stress biomarkers.
Steven V. Edelman, MD is a
renowned endocrinologist and diabetes specialist, currently serving
as a Professor of Medicine in the Division of Endocrinology,
Diabetes, and Metabolism at the University of California, San Diego
(UCSD). He is also the founder and director of Taking Control of
Your Diabetes (TCOYD), a not-for-profit organization dedicated to
educating and empowering individuals with diabetes to manage their
condition effectively. Dr. Edelman completed his medical education
at the University of California, Davis, followed by a residency in
internal medicine at the University of California, Los Angeles
(UCLA). He further specialized in endocrinology and metabolism
during his fellowship at the Joslin Diabetes Center in Boston. His
research interests include diabetes management, patient education,
and the development of new therapies for diabetes. Dr. Edelman has
been involved in numerous clinical trials and has published
extensively in the field of diabetes care.
Franco Folli, MD, PhD is an
internist and diabetes researcher, currently a Professor of
Endocrinology and Metabolism at the Department of Health Sciences,
Universita’ degli Studi di Milano and affiliated with ASST Santi
Paolo e Carlo in Milan, Italy. He earned his medical degree and
Ph.D. from the Università di Milano. Dr. Folli's research focuses
on inflammation, insulin signaling, and the pathophysiology of
diabetes, significantly advancing the understanding of insulin
resistance and inflammation in diabetes. Previously, he was a
Professor of Internal Medicine (with tenure) at the University of
Texas Health Science Center at San Antonio, where he conducted
groundbreaking clinical and basic research on diabetes. Supported
by grants, from the Italian Ministry of Health, Telethon, National
Institute of Health (USA), Dr. Folli has pioneered work on the
molecular mechanisms of insulin action and resistance.
Francesco Giorgino, MD, PhD is
an endocrinologist and diabetes researcher, currently Professor of
Endocrinology and Chairman of the Department of Precision and
Regenerative Medicine at the University of Bari Aldo Moro, and
Chief of the Division of Endocrinology at University Hospital
Policlinico Consorziale in Bari, Italy. He has held leadership
positions, including President of the Italian Society of
Endocrinology (SIE) and Senior Vice President of the European
Association for the Study of Diabetes (EASD). Dr. Giorgino has been
also the Director of the Specialty School of Endocrinology and
Metabolism at the University of Bari for several years, mentoring
future endocrinologists. Dr. Giorgino research focuses on insulin
resistance, beta-cell dysfunction, and the effects of diabetes
drugs on pancreatic islets and the cardiovascular system. His
notable studies include research on SGLT2 inhibitors and GLP-1
receptor agonists, impacting glycemic control and cardiovascular
outcomes.
Freddy Goldberg Eliaschewitz,
MD is a prominent endocrinologist and diabetes researcher,
currently the Director at CPClin Clinical Research Center in São
Paulo, Brazil. He completed his medical degree and master's in
Endocrinology at Universidade de São Paulo. Dr. Eliaschewitz has
contributed significantly to clinical research and patient care at
Hospital Israelita Albert Einstein in São Paulo. His research
focuses on diabetes, particularly glycemic control, insulin
therapy, and preventing diabetic complications. He has led numerous
clinical trials, including the GOAL study and IDMPS, exploring the
efficacy of ultra-long basal insulins like degludec. Dr.
Eliaschewitz has served as a consultant and advisory board member
for major pharmaceutical companies and published extensively in
peer-reviewed journals. His work on insulin therapy and diabetes
management has advanced treatment practices, especially in low- and
middle-income countries.
Mohamed Hassanein, MD is a
Senior Consultant in Endocrinology and Diabetes at Dubai Hospital,
UAE, since 2014, and a Senior Lecturer and Associate Director for
Postgraduate Diabetes Education at Cardiff University, UK, since
2007. He graduated from the Faculty of Medicine, Alexandria, Egypt,
and is renowned for his research on diabetes management during
Ramadan. Dr. Hassanein has co-authored influential guidelines,
including those for the American Diabetes Association and the
IDF-DAR practical guidelines. He has published over 70 papers and
presented at more than 50 conferences, focusing on the safety and
efficacy of diabetes treatments, like SGLT2 inhibitors, during
fasting. His research includes flash glucose monitoring and insulin
pump therapy. Dr. Hassanein has been recognized with several
awards, including the SAHF Lifetime Achievement Award in 2022.
Steven E. Kahn, MB, ChB is the
Leonard L. Wright & Marjorie C. Wright Term Chair of Medicine
and Professor of Medicine at the University of Washington (UW). He
also serves as a Staff Physician at the VA Puget Sound Health Care
System and Director of the UW Diabetes Research Center. Dr. Kahn
earned his medical degree from the University of Cape Town and
completed his endocrine fellowship at UW. His research focuses on
the pathophysiology of type 2 diabetes, specifically islet
beta-cell dysfunction and insulin resistance. He has significantly
contributed to understanding how islet amyloid formation leads to
beta-cell loss and hyperglycemia. Involved in major clinical trials
like the Diabetes Prevention Program (DPP) and the Restoring
Insulin Secretion (RISE) Study, Dr. Kahn has published over 730
peer-reviewed articles. He has received numerous awards, including
the American Diabetes Association Outstanding Achievement in
Clinical Diabetes Research Award and European Association for the
Study of Diabetes Claude Bernard Award. He currently serves as
editor-in-chief of Diabetes Care.
Rohit N. Kulkarni, MD, PhD is a
physician scientist and diabetes researcher, serving as a Professor
of Medicine at Harvard Medical School and holds the Diabetes
Research and Wellness Foundation Chair. He is Co-Head of the
Section on Islet and Regenerative Biology at the Joslin Diabetes
Center, Principle Faculty of the Harvard Stem Cell Institute and
Associate Member of the Broad Institute. Dr. Kulkarni's research
focuses on pathways in islet cell biology that are critical to
understand the pathophysiology of both type 1 and type 2 diabetes.
His lab investigates growth factor receptors (e.g. insulin, IGF-1),
mRNA modifications, and cross talk with incretin signaling. His lab
has expertise in generating patient-derived induced pluripotent
stem (iPS) cells for differentiation into insulin- or
glucagon-secreting cells for potential therapeutic applications.
Dr. Kulkarni has received numerous accolades, including the Ernst
Oppenheimer Award (Endocrine Society), the Albert Renold Prize
(European Association for Study of Diabetes) and Paul E. Lacy Medal
(Midwest Islet Consortium), and is an elected Fellow of the
American Society for Clinical Investigation, the Association of
American Physicians and the American Association for the
Advancement of Science.
Chantal Mathieu, MD is a
renowned endocrinologist and diabetes researcher, currently a
Professor of Medicine at KU Leuven in Belgium and Chair of
Endocrinology at University Hospital Gasthuisberg Leuven. She
earned her M.D. and Ph.D. from the University of Leuven and trained
in internal medicine and endocrinology there. Dr. Mathieu's
research focuses on the prevention of type 1 diabetes, the effects
of vitamin D on the immune system, and the functioning of
insulin-producing beta cells. Notably, she coordinates the EDENT1FI
project, a European initiative aimed at exploring screening
strategies and early diagnosis of type 1 diabetes. She is Chair of
the Board of the INNODIA initiative, a network of clinical trial
sites for interventions in type 1 diabetes in Europe. Her
contributions have earned her prestigious awards, including the
InBev-Baillet Latour Prize for Clinical Research and the David
Rumbough Award from the JDRF for her research on the
pathophysiology of type 1 diabetes. Dr. Mathieu is also the
President of the European Association for the Study of Diabetes
(EASD).
Jeremy Pettus, MD is an
Associate Professor of Medicine in the Department of Endocrinology
at the University of California, San Diego (UCSD), where he
specializes in diabetes care and research. After earning his
medical degree from Boston University School of Medicine, he
completed his residency and fellowship in Endocrinology at UCSD.
Dr. Pettus is actively involved in clinical trials, focusing on new
therapies for type 1 diabetes, including glucagon receptor
antagonists and the development of the artificial pancreas. His
work is widely recognized, and he is a frequent speaker at national
and international conferences. In addition to his research, Dr.
Pettus is committed to patient education through his involvement
with the non-profit Taking Control of Your Diabetes (TCOYD), where
he leads the Type 1 Diabetes track at national conferences. His
clinical practice emphasizes personalized care, understanding the
unique challenges faced by people with diabetes. With a focus on
patient empowerment and innovative treatments, Dr. Pettus continues
to make impactful contributions to the field of diabetes
management.
Julio Rosenstock, MD is a
renowned endocrinologist and expert in type 2 diabetes, serving as
the Director of the Dallas Diabetes Research Center at Medical City
Dallas and Clinical Professor of Medicine at the University of
Texas Southwestern Medical Center. He earned his medical degree
from Universidad Nacional Autónoma de México and completed his
residency and fellowship at UT Southwestern. Dr. Rosenstock's
research focuses on novel therapeutic strategies for optimal
glycemic control in type 2 diabetes. He has led numerous clinical
trials, contributing to the development of new oral antidiabetic
agents, incretin-based therapies, and insulin preparations. His
recent work includes research on insulin icodec, a potential
once-weekly basal insulin. Dr. Rosenstock holds leadership
positions, including Senior Scientific Advisor for Velocity
Clinical Research, and serves on advisory boards for pharmaceutical
companies.
Desmond Schatz, MD is a highly
esteemed pediatric endocrinologist and expert in type 1 diabetes
research. He serves as a Professor of Pediatrics and the Medical
Director of the Diabetes Institute at the University of Florida
(UF), as well as the Director of the Clinical Research Center
within UF's Clinical and Translational Science Institute (CTSI).
Dr. Schatz earned his medical degree in South Africa. His research
focuses on the prediction, natural history, genetics,
immunopathogenesis, and prevention of type 1 diabetes, alongside
developing new treatment strategies. He has been a key investigator
in the Diabetes Prevention Trial and TrialNet and other multicenter
studies. Dr. Schatz has received numerous accolades, including the
Banting Award and JDRF's highest research award. He was honored
with the UF College of Medicine Lifetime Achievement Award in 2020
and is a member of the Academy of Science and Medicine for Florida,
and was a past president of the American Diabetes Association
(ADA).
Jay S. Skyler, MD is a
distinguished endocrinologist and diabetes researcher, currently a
Professor of Medicine, Pediatrics, and Psychology at the University
of Miami Miller School of Medicine, where he also serves as Deputy
Director for Clinical Research and Academic Programs at the
Diabetes Research Institute. Dr. Skyler earned his medical degree
from Jefferson Medical College and completed his training in
Internal Medicine and Endocrinology at Duke University Medical
Center. His research focuses on type 1 diabetes, particularly
immune intervention strategies. He has led numerous clinical
trials, including the NIH-sponsored Diabetes Prevention Trial for
Type 1 Diabetes (DPT-1) and the Type 1 Diabetes TrialNet Clinical
Trials Study Group. Dr. Skyler has received numerous awards, such
as the Banting Medal, the Distinction in Endocrinology Award from
the American College of Endocrinology, and the JDRF's Mary Tyler
Moore/S. Robert Levine Award. Dr. Skyler has held leadership roles
as President of the ADA, Vice-President of the International
Diabetes Federation, and President of the International Diabetes
Immunotherapy Group. He was the founding Editor-in-Chief of
Diabetes Care and serves on multiple editorial boards.
Kohjiro Ueki, MD, PhD is a
distinguished endocrinologist and diabetes researcher, currently
serving as the Director of the Diabetes Research Center at the
National Center for Global Health, Japan. He also served as
Professor of the Department of Molecular Diabetology, Graduate
School of Medicine, the University of Tokyo where he earned his
medical degree and PhD. Dr. Ueki's research focuses on insulin
resistance, insulin secretion, and the pathogenesis of type 2
diabetes. He serves as the Chair of the Board of Directors of the
Japan Diabetes Society and has been instrumental in developing
clinical practice guidelines, including the "Kumamoto Declaration
2013". He has conducted significant studies on the efficacy and
safety of diabetes treatments and the role of pancreatic alpha-cell
function in insulin sensitivity. Supported by grants from
prestigious organizations, Dr. Ueki has received numerous awards
for his contributions.
About 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 patients were enrolled in
single ascending dose cohorts to evaluate safety at the prospective
dosing levels for type 2 diabetic patients. Phase II consists of
multiple ascending dose cohorts and includes adult patients with
type 2 diabetes uncontrolled by standard of care medicines. Once
the Escalation Phase of COVALENT-111 was completed, the study
advanced into an Expansion Phase (Ph IIb) consisting of multiple
cohorts dosing type 2 diabetes patients for longer dose durations.
Additional information about this Phase I/II clinical trial of
BMF-219 in type 2 diabetes can be found at ClinicalTrials.gov using
the identifier NCT05731544.
About COVALENT-112
COVALENT-112 is a multi-site, randomized,
double-blind, placebo-controlled Phase II study in adults with
stage 3 type 1 diabetes. This stage describes the period following
clinical diagnosis of type 1 diabetes when symptoms are present due
to significant beta cell loss. COVALENT-112 will be a multi-arm
trial comparing two different doses of BMF-219 to placebo (1:1:1)
to evaluate the efficacy, safety, and durability of BMF-219 in
adults with type 1 diabetes. Approximately 150 patients will be
enrolled in the trial and will receive either BMF-219 or placebo
over 12 weeks, followed by a 40-week off treatment period.
This trial also includes an open-label portion
for adults with type 1 diabetes up to 15 years since diagnosis. The
open-label portion (n=40) is examining the efficacy, safety, and
durability of BMF-219 at two oral dose levels, 100 mg and 200 mg
over 12-week treatment followed by a 40-week off treatment
period.
Additional information about the Phase II
clinical trial of BMF-219 in type 1 diabetes can be found at
ClinicalTrials.gov using the identifier NCT06152042.
About Biomea Fusion
Biomea Fusion is a clinical stage
biopharmaceutical company focused on the discovery and development
of oral covalent small molecules to treat patients with metabolic
diseases and genetically defined cancers. 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. 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 expected contributions of our scientific
advisory board, the clinical and therapeutic potential of our
product candidates and development programs, including BMF-219, the
potential of BMF-219 as a treatment for type 1 and type 2 diabetes,
our research, development and regulatory plans, the progress of our
ongoing and upcoming clinical trials, including our Phase I/II
COVALENT-111 study of BMF-219 in type 2 diabetes, and our Phase II
COVALENT-112 study of BMF-219 in type 1 diabetes, 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 in preclinical or clinical development,
patient enrollment and in the initiation, conduct and completion of
our ongoing and planned clinical trials and other research and
development 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
Associate Director of Investor Relations & Corporate Development
czhao@biomeafusion.com
Media Relations
Neera Chaudhary, MHSc RD
nchaudhary@biomeafusion.com
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