Pacira Announces the Presentation of 104-Week Safety and Efficacy Data Following Local Administration of PCRX-201 for Moderate to Severe Osteoarthritis of the Knee
September 26 2024 - 8:00AM
Pacira BioSciences, Inc. (NASDAQ: PCRX), the industry leader in the
delivery of innovative, non-opioid pain therapies, today announced
the upcoming presentation of new data in support of its gene
therapy candidate, PCRX-201 (enekinragene inzadenovec). The data
will be presented at the American College of Rheumatology’s annual
ACR Convergence meeting, being held in Washington, D.C. November
14–19.
Presentation Title: Sustained
Clinical Effects After a Single Intra-articular Injection of
PCRX-201 for Moderate-to-Severe Osteoarthritis of the Knee
Presented By: Stanley Cohen, MD,
a board-certified rheumatologist and Co-Medical Director of the
Metroplex Clinical Research Center in Dallas, TX
Date & Time: Sunday, November
17 from 10:30 am – 12:30 pm EST
PCRX-201 is a locally administered gene therapy,
designed to produce interleukin-1 receptor antagonist (IL-1Ra), a
naturally occurring, anti-inflammatory protein with a proven
mechanism of action that reduces interleukin-1 (IL-1) signaling, a
known factor in the development and progression of osteoarthritis
of the knee. Unlike systemically administered gene therapies,
PCRX-201 delivers the medicine where it matters and uses an
inducible promoter to mimic the body’s natural response to
inflammation by “turning on” the expression of IL-1Ra when
inflammation is present in the joint to reduce pain and disability
and potentially slow structural progression.
In March 2024, PCRX-201 became the first-ever gene
therapy product candidate in osteoarthritis to receive Regenerative
Medicine Advanced Therapy (RMAT) designation from the U.S. Food and
Drug Administration (FDA).
RMAT designation provides the benefits of
intensive FDA guidance on efficient drug development, including the
ability for early interactions with the FDA to discuss surrogate or
intermediate endpoints, potential ways to support accelerated
approval and satisfy post-approval requirements, potential priority
review of the Biologics License Application (BLA), and other
opportunities to expedite development and review. PCRX-201 was also
granted Advanced Therapy Medicinal Products (ATMP) designation by
the European Medicines Agency in May 2023.
About Pacira BioSciences Pacira
BioSciences delivers innovative, non-opioid pain therapies to
transform the lives of patients. Pacira has three commercial-stage
non-opioid treatments: EXPAREL® (bupivacaine liposome injectable
suspension), a long-acting local analgesic currently approved for
infiltration, fascial plane block, and as an interscalene brachial
plexus nerve block for postsurgical pain management; ZILRETTA®
(triamcinolone acetonide extended-release injectable suspension),
an extended-release, intra-articular injection indicated for the
management of osteoarthritis knee pain; and ioveraº®, a novel,
handheld device for delivering immediate, long-acting, drug-free
pain control using precise, controlled doses of cold temperature to
a targeted nerve. The company is also advancing the development of
PCRX-201, a novel locally administered gene therapy with the
potential to treat large prevalent diseases like osteoarthritis. To
learn more about Pacira, visit www.pacira.com.
Investor Contact:
Susan Mesco, (973) 451-4030
susan.mesco@pacira.com
Media Contact:
Sara Marino, (973) 248-7005
Sara.marino@pacira.com
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