Scilex Holding Company (Nasdaq: SCLX, “Scilex” or “Company”) and
IPMC Company, a representative company of the Bio Innovation
Consortium (“BOIC”), which holds the exclusive rights to
NeuroBiogen Company’s (“NB”) KDS2010 global license, today
announced a binding term sheet to create a commercial joint
venture, Scilex Bio, to develop and commercialize a next-generation
reversible MAO-B Inhibitor, a novel inhibitor of aberrant GABA
production in reactive astrocytes for the treatment of obesity and
neurodegenerative diseases including Alzheimer’s disease.
IPMC, a private biopharmaceutical company, represents the BOIC,
an innovative consortium committed to establishing 'Open
Innovation' as a transformative paradigm in biohealth research,
development, and commercialization.
“The partnership between IPMC and Scilex spans almost a decade.
At the 2017 IPMC International Conference in Seoul, leaders from
both companies pledged to undertake a bold challenge for the next
century, dedicated to upholding the dignity of human life. Since
then, we have been deeply impressed by Scilex's efforts in
advancing multiple non-opioid pain management programs, addressing
areas of significant unmet medical needs in the U.S. and beyond. We
believe Scilex is uniquely positioned to unlock the potential of
KDS2010, offering hope to individuals suffering from
neurodegenerative and cardiometabolic diseases. This potential
milestone represents a significant advancement in fulfilling the
vision of our bold challenge,” said Youngwoo Jang, President of
IPMC.
“We are thrilled to partner with IPMC and BOIC to advance
KDS2010, a promising oral therapy targeting some of the most
pressing global health challenges, including obesity and
neurodegenerative diseases, which affect over a billion people
globally. By leveraging IPMC’s groundbreaking work on KDS2010 and
Scilex’s strengths in development and commercialization, we believe
this novel oral therapy may redefine treatment standards, offering
a safer and more convenient solution for patients with obesity and
other CNS diseases,” said Jaisim Shah, President and Chief
Executive Officer of Scilex.
“KDS2010 has the potential to significantly advance treatment
options for obesity and neurodegenerative diseases, areas where
current therapies often fall short. With its innovative mechanism
and favorable safety profile, this small molecule offers a unique
opportunity to deliver better outcomes for patients. We are eager
to bring this groundbreaking therapy to market,” said Dr. Jay Chun,
M.D., Ph.D., board member of Scilex.
The formation and organizational structure of Scilex Bio JV is
subject to negotiation of definitive agreements between Scilex and
IPMC, with operations of Scilex Bio JV expected to commence during
Q1-2025.
For more information on Scilex Holding Company, refer to
www.scilexholding.com.
For more information on Semnur Pharmaceuticals, refer to
www.semnurpharma.com.
For more information on Scilex Holding Company Sustainability
Report, refer to
www.scilexholding.com/investors/sustainability.
For more information on ZTlido®, including Full Prescribing
Information, refer to www.ztlido.com.
For more information on ELYXYB®, including Full Prescribing
Information, refer to www.elyxyb.com.
For more information on Gloperba®, including Full Prescribing
Information, refer to www.gloperba.com.
https://www.facebook.com/scilex.pharm
https://www.linkedin.com/company/scilex-holding-company/
info@scilexholding.com
About Scilex Holding Company
Scilex Holding Company is an innovative revenue-generating
company focused on acquiring, developing and commercializing the
treatment for neurodegenerative and cardiometabolic diseases, and
non-opioid pain management products for the treatment of acute and
chronic pain. Scilex targets indications with high unmet needs and
large market opportunities with non-opioid therapies for the
treatment of patients with acute and chronic pain and is dedicated
to advancing and improving patient outcomes. Scilex’s commercial
products include: (i) ZTlido® (lidocaine topical system) 1.8%, a
prescription lidocaine topical product approved by the U.S. Food
and Drug Administration (the “FDA”) for the relief of neuropathic
pain associated with postherpetic neuralgia, which is a form of
post-shingles nerve pain; (ii) ELYXYB®, a potential first-line
treatment and the only FDA-approved, ready-to-use oral solution for
the acute treatment of migraine, with or without aura, in adults;
and (iii) Gloperba®, the first and only liquid oral version of the
anti-gout medicine colchicine indicated for the prophylaxis of
painful gout flares in adults.
In addition, Scilex has three product candidates: (i) SP-102 (10
mg, dexamethasone sodium phosphate viscous gel) (“SEMDEXA™” or
“SP-102”), a novel, viscous gel formulation of a widely used
corticosteroid for epidural injections to treat lumbosacral
radicular pain, or sciatica, for which Scilex has completed a Phase
3 study and was granted Fast Track status from the FDA in 2017;
(ii) SP-103 (lidocaine topical system) 5.4%, (“SP-103”), a
next-generation, triple-strength formulation of ZTlido, for the
treatment of acute pain and for which Scilex has recently completed
a Phase 2 trial in acute low back pain. SP-103 has been granted
Fast Track status from the FDA in low back pain; and (iii) SP-104
(4.5 mg, low-dose naltrexone hydrochloride delayed-release
capsules) (“SP-104”), a novel low-dose delayed-release naltrexone
hydrochloride being developed for the treatment of fibromyalgia,
for which Phase 1 trials were completed in the second quarter of
2022.
Scilex Holding Company is headquartered in Palo Alto,
California.
For more information on Scilex Holding Company, refer to
www.scilexholding.com
About Semnur Pharmaceuticals, Inc.
Semnur Pharmaceuticals, Inc. (“Semnur”) is a clinical,
late-stage specialty pharmaceutical company focused on the
development and commercialization of novel non-opioid pain
therapies. Semnur’s lead program, SP-102 (SEMDEXA™), is the first
non-opioid novel gel formulation administered epidurally in
development for patients with moderate to severe chronic radicular
pain/sciatica.
Semnur Pharmaceuticals, Inc. is headquartered in Palo Alto,
California.
For more information on Semnur Pharmaceuticals, refer to
www.semnurpharma.com
About IPMC
IPMC is a private biopharmaceutical company, represents the
BOIC, an innovative consortium committed to establishing 'Open
Innovation' as a transformative paradigm in biohealth research,
development, and commercialization.
Forward-Looking Statements
This press release and any statements made for and during any
presentation or meeting concerning the matters discussed in this
press release contain forward-looking statements related to Scilex
and its subsidiaries and are subject to risks and uncertainties
that could cause actual results to differ materially from those
projected. Forward-looking statements include statements Scilex and
its subsidiaries, including but not limited to Semnur, statements
regarding the terms of the potential joint venture transaction,
statements regarding KDS2010 and the potential efficacy and
preclinical results, the potential for KDS2010 to be an innovative
new treatment for obesity and Alzheimer’s disease benefitting
people living with neurodegenerative and cardiometabolic diseases,
the potential market size and growth opportunity for the weight
loss and Alzheimer’s global drug market, the timing of formation
and operations of Scilex Bio JV , the expectation that Semnur
common stock will be publicly traded on Nasdaq during Q1-2025,
statements regarding the Company’s outlook, goals and expectations
for 2024, and the Company’s development and commercialization
plans. Although Scilex and its subsidiaries believe that they have
a reasonable basis for each forward-looking statement contained in
this press release Scilex and its subsidiaries caution you that
these statements are based on a combination of facts and factors
currently known and projections of the future, which are inherently
uncertain.
Risks and uncertainties that could cause actual results of
Scilex to differ materially and adversely from those expressed in
our forward-looking statements, include, but are not limited to:
the inability of the parties to complete the joint venture
transaction, changes in timing of the proposed joint venture
transaction and the ability of the parties to achieve the benefits
of the proposed joint venture transaction risks associated with the
unpredictability of trading markets; general economic, political
and business conditions; the risk that the potential product
candidates that Scilex develops may not progress through clinical
development or receive required regulatory approvals within
expected timelines or at all; risks relating to uncertainty
regarding the regulatory pathway for Scilex’s product candidates;
the risk that Scilex will be unable to successfully market or gain
market acceptance of its product candidates; the risk that Scilex’s
product candidates may not be beneficial to patients or
successfully commercialized; the risk that Scilex has overestimated
the size of the target patient population, their willingness to try
new therapies and the willingness of physicians to prescribe these
therapies; risks that the outcome of the trials and studies for
SP-102, SP-103 or SP-104 may not be successful or reflect positive
outcomes; risks that the prior results of the clinical and
investigator-initiated trials of SP-102 (SEMDEXA™), SP-103 or
SP-104 may not be replicated; regulatory and intellectual property
risks; and other risks and uncertainties indicated from time to
time and other risks described in Scilex’s most recent periodic
reports filed with the SEC, including the Annual Report on Form
10-K for the year ended December 31, 2023 and subsequent Quarterly
Reports on Form 10-Q that the Company has filed or may file,
including the risk factors set forth in those filings. Investors
are cautioned not to place undue reliance on these forward-looking
statements, which speak only as of the date of this release, and
Scilex undertakes no obligation to update any forward-looking
statement in this press release except as may be required by
law.
Contacts:
Investors and MediaScilex Holding Company 960 San Antonio
RoadPalo Alto, CA 94303Office: (650) 516-4310
Email: investorrelations@scilexholding.com
Website: www.scilexholding.com
References
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www.reuters.com/business/healthcare-pharmaceuticals/weight-loss-drug-forecasts-jump-150-billion-supply-grows-2024-05-28/
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www.ihealthcareanalyst.com/global-alzheimers-disease-market/
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https://idf.org/news/one-billion-people-globally-estimated-to-be-living-with-obesity-by-2030/
SEMDEXA™ (SP-102) is a trademark owned by Semnur
Pharmaceuticals, Inc., a wholly-owned subsidiary of Scilex Holding
Company. A proprietary name review by the FDA is planned.
ZTlido® is a registered trademark owned by
Scilex Pharmaceuticals Inc., a wholly-owned subsidiary of Scilex
Holding Company.
Gloperba® is the subject of an exclusive,
transferable license to Scilex Holding Company to use the
registered trademark.
ELYXYB® is a registered trademark owned by
Scilex Holding Company.
Scilex Bio™ is a trademark owned by Scilex
Holding Company.
All other trademarks are the property of their
respective owners.
© 2024 Scilex Holding Company All Rights
Reserved.
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