Lexicon Announces Completion of Enrollment in Phase 2B PROGRESS Study of LX9211 in Diabetic Peripheral Neuropathic Pain (DPNP)
November 26 2024 - 8:00AM
Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX) today announced the
completion of patient enrollment in the
PROGRESS (A
Phase 2b,
Dose-ranging,
Randomized, Double-blind,
Placeb
O-controlled,
Parallel-
GRoup,
Multic
Enter
Study with an
Open-label Extension in Patient
S with
Diabetic Peripheral Neuropathic Pain) study evaluating LX9211,
a novel, orally-delivered, selective investigational small molecule
inhibitor of adaptor-associated kinase 1 (AAK1), for the treatment
of diabetic peripheral neuropathic pain (DPNP).
The study successfully enrolled 494 patients, approximately 20
percent more than originally targeted, marking a significant
milestone in the trial and increasing study power. Top-line data
from PROGRESS is expected to be announced in Q1 2025.
"We are pleased to have completed enrollment for the PROGRESS
study of LX9211 in DPNP, a condition for which there is significant
need for new, non-opioid treatment options," said Craig Granowitz,
M.D., Ph.D., Lexicon’s senior vice president and chief medical
officer. "The strong interest in this study resulted in enrollment
significantly exceeding the target and completion of enrollment
eight weeks ahead of schedule, underscoring the urgent demand in
DPNP. We are confident that the greater-than-expected enrolled
patient population will lead to critical insights, inform our Phase
3 design and add to the body of evidence supporting the use of
LX911 in treating neuropathic pain and we look forward to sharing
top-line findings from the study early next year."
About the PROGRESS StudyPROGRESS commenced in
December of 2023 with the goal of enrolling adult patients with a
diagnosis of diabetes (type 1 or type 2) with moderate to severe
DPNP. The study is placebo-controlled with a primary endpoint of
reduction of Average Daily Pain Score (ADPS) at 8 weeks. Secondary
endpoints include change from baseline in burning pain and pain
interference with sleep. Study design permitted patients to
maintain one stable-dose DPNP therapy (gabapentin, pregabalin or
duloxetine) without being forced to withdraw from therapies that,
although inadequate, may be providing benefit – aligning with how
new DPNP drugs are likely to be used in practice.
About DPNPDPNP is a type of nerve damage
caused by chronically high blood sugar and is a major disabling and
devastating consequence of long-term diabetes. It can result in
pain, numbness, and other symptoms in the hands, feet, legs, and
arms. There are approximately 20 million patients in the U.S. who
are suffering with some type of neuropathic pain, of which about 5
million have DPNP.
About LX9211Discovered using Lexicon’s unique
approach to gene science, LX9211 is a potent, orally delivered,
selective, investigational small molecule inhibitor of AAK1.
Lexicon identified AAK1 in its target discovery efforts as a
promising approach for the treatment of neuropathic pain.
Preclinical studies of LX9211 demonstrated central nervous system
penetration and reduction in pain behavior in models of neuropathic
pain without affecting opiate pathways. LX9211 received Fast Track
designation from the U.S. Food and Drug Administration for
development in DPNP.
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 a pipeline of promising drug candidates in
discovery and clinical and preclinical development in neuropathic
pain, hypertrophic cardiomyopathy (HCM), obesity, metabolism and
other indications. For additional information, please visit
www.lexpharma.com.
Safe Harbor StatementThis press
release contains “forward-looking statements,” including statements
relating to Lexicon’s financial position and long-term outlook on
its business, growth and future operating results, discovery and
development 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,
conduct preclinical and clinical development and obtain necessary
regulatory approvals of sotagliflozin, LX9211, LX9851 and 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 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 and other subsequent
disclosure documents 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.
Investors and MediaLisa DeFrancescoLexicon
Pharmaceuticals, Inc.lexinvest@lexpharma.com
Lexicon Pharmaceuticals (NASDAQ:LXRX)
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