Lexicon to Present Phase 3 Trial Design for Sotagliflozin in Hypertrophic Cardiomyopathy (HCM) at Upcoming Medical Congress
27 Settembre 2024 - 2:00PM
Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX) today announced that
it will unveil study design details of SONATA-HCM, the company’s
Phase 3 clinical trial of sotagliflozin as a potential new
treatment for adults with hypertrophic cardiomyopathy (HCM), at the
virtual Hypertrophic Cardiomyopathy Medical Society (HCMS) 2024
Scientific Sessions. Lexicon plans to conduct the multinational
study at 130 sites in 20 countries and enroll adults aged 18 years
or older diagnosed with symptomatic HCM, either obstructive (oHCM)
or non-obstructive (nHCM). Initial study sites have been activated
and patient randomization is underway.
Details for the presentation on “A Randomized, Double-Blind,
Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate
the Efficacy and Safety of
SOtaglifloziN in Patients with
SymptomATic obstructive And
non-obstructive Hypertrophic
CardioMyopathy (SONATA-HCM)” is
as follows:
- HCMS (virtual) – a moderated poster presentation, Friday,
September 27, 2:00-2:30p.m. ET, presented by Carolyn Y. Ho, M.D.,
Cardiology, Brigham and Women’s Hospital, Boston, MA
The estimated prevalence of HCM in the United States is about
1.1 million. The most common patient-reported symptoms include
shortness of breath, lightheadedness or dizziness, fatigue, heart
fluttering or palpitations, and limitations to physical
activities.
“SONATA-HCM will evaluate the efficacy of sotagliflozin, a dual
SGLT2 and SGLT1 inhibitor, on symptoms, function, and other
patient-reported outcomes, as well as safety in patients with
symptomatic HCM,” said Dr. Ho, M.D., Cardiology, Brigham and
Women’s Hospital, and a co-author of the study abstract.
“Despite recent advances in the treatment of HCM, there remain
significant needs among patients and clinicians for new therapeutic
options,” said Sharlene M. Day, M.D., Director, Translational
Research, Division of Cardiovascular Medicine and Cardiovascular
Institute, Presidential Associate Professor, University of
Pennsylvania Medicine, and a co-author of the study abstract.
“Although HCM is a unique condition, there are overlapping features
with other conditions that lead to heart failure, so I’m optimistic
that sotagliflozin could work in this patient population.”
“We are excited about the potential for sotagliflozin to become
a safe and effective treatment for HCM, either as standalone
therapy or in conjunction with currently available medications,”
said Craig Granowitz, M.D., Ph.D., Lexicon’s senior vice president
and chief medical officer. “Based on our interactions with FDA, and
if supported by positive study results, we plan to submit a
supplemental new drug application (sNDA) with a broad proposed
label to improve symptoms and physical limitations in adults with
HCM.”
For more information on the study, visit the SONATA-HCM page on
ClinicalTrials.gov.
About SotagliflozinDiscovered using Lexicon’s
unique approach to gene science, sotagliflozin is an oral inhibitor
of two proteins responsible for glucose regulation known as
sodium-glucose cotransporter types 2 and 1 (SGLT2 and SGLT1). SGLT2
is responsible for glucose and sodium reabsorption by the kidney
and SGLT1 is responsible for glucose and sodium absorption in the
gastrointestinal tract. Sotagliflozin has been studied in multiple
patient populations encompassing heart failure, diabetes, and
chronic kidney disease in clinical studies involving approximately
20,000 patients.
About Lexicon Pharmaceuticals Lexicon is a
biopharmaceutical company with a mission of pioneering medicines
that transform patients’ lives. Through the Genome5000™ program,
Lexicon’s unique genomics target discovery platform, Lexicon
scientists studied the role and function of nearly 5,000 genes and
identified more than 100 protein targets with significant
therapeutic potential in a range of diseases. Through the precise
targeting of these proteins, Lexicon is pioneering the discovery
and development of innovative medicines to treat disease safely and
effectively. Lexicon has commercially launched one of these
medicines, INPEFA® (sotagliflozin) in the United States, and has a
pipeline of other promising drug candidates in discovery and
clinical and preclinical development in neuropathic pain, diabetes
and metabolism and other indications. For additional information,
please visit www.lexpharma.com.
Safe Harbor Statement
This press release contains “forward-looking statements,”
including statements relating to Lexicon’s financial position and
long-term outlook on its business, including the commercialization
of its approved products and the clinical development of,
regulatory filings for, and potential therapeutic and commercial
potential of its other drug candidates. In addition, this press
release also contains forward looking statements relating to
Lexicon’s growth and future operating results, discovery,
development and commercialization of products, strategic alliances
and intellectual property, as well as other matters that are not
historical facts or information. All forward-looking statements are
based on management’s current assumptions and expectations and
involve risks, uncertainties and other important factors,
specifically including Lexicon’s ability to meet its capital
requirements, successfully commercialize its approved products,
successfully conduct preclinical and clinical development and
obtain necessary regulatory approvals of its other drug candidates
on its anticipated timelines, achieve its operational objectives,
obtain patent protection for its discoveries and establish
strategic alliances, as well as additional factors relating to
manufacturing, intellectual property rights, and the therapeutic or
commercial value of its approved products and other drug
candidates. Any of these risks, uncertainties and other factors may
cause Lexicon’s actual results to be materially different from any
future results expressed or implied by such forward-looking
statements. Information identifying such important factors is
contained under “Risk Factors” in Lexicon’s annual report on Form
10-K for the year ended December 31, 2023, as filed with the
Securities and Exchange Commission. Lexicon undertakes no
obligation to update or revise any such forward-looking statements,
whether as a result of new information, future events or
otherwise.
For Investor and Media
Inquiries:Lisa DeFrancesco Lexicon Pharmaceuticals,
Inc.lexinvest@lexpharma.com
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