Sorrento to Host Webcast to Discuss Newly Presented Clinical Data Demonstrating Significant Improvements in Therapeutic Outcomes in 10 of 10 Patients with Poorly Controlled Rheumatoid Arthritis
November 13 2022 - 2:02PM
Sofusa®, a wholly-owned division of Sorrento Therapeutics (Nasdaq:
SRNE, “Sorrento”), today announced that it will host a virtual Key
Opinion Leader (KOL) panel discussion titled “Empowering the
Lymphatics: Unleashing the Potential of Biologics that Target the
Immune System” to be held on Thursday, November 17, 2022 at 11:30
AM EST.
The event will feature a deep dive and discussion of the
clinical study design and clinical data demonstrating improved
therapeutic outcomes and lymphatic functioning in rheumatoid
arthritis (RA) patients receiving the Sofusa Lymphatic Drug
Delivery System (Sofusa) treatment. Patients who were enrolled in
this study had inadequate response to the standard dose of an
approved TNF inhibitor subcutaneous (SC) treatment, and 10 of 10
patients achieved a significant improvement in disease activity and
lymphatic function following initiation of Sofusa lymphatic
treatment, with dose levels at half of the prior SC dose or less.
This data was accepted and presented today at the American College
of Rheumatology (ACR) Convergence 2022 meeting in Philadelphia.
Chris Jeffers, Ph.D., J.D., Chief Executive Officer of Mayflower
BioVentures and Hibiscus BioTechnology, will moderate this panel
discussion following the ACR conference. Speakers for the event
include:
- Roel Querubin, M.D., Board Certified
Rheumatologist, Atlanta Research Center for Rheumatology and
Marrieta Rheumatology Associates
- Vibeke Strand, M.D. Adjunct Clinical
Professor, Division of Immunology and Rheumatology, Stanford
University School of Medicine
- Mike Royal, M.D., Chief Medical
Officer, Sorrento
- Brian Cooley, Senior Vice President,
Head of Sofusa Lymphatic Drug Development
- Russell Ross, Ph.D., Chief Technical
Officer, Sofusa Lymphatic Drug Development
To register for the live event, please visit the Online
Experiences website. Detailed biographies for all the speakers can
be accessed here.
Following the live webcast, an archived replay will be available
on the Company’s website at Events Calendar - Sorrento
Therapeutics.
About Sorrento’s Sofusa Business Unit
The Sofusa Business Unit is a wholly owned division of Sorrento
based in Atlanta, Georgia and is focused on lymphatic drug
development with pre-clinical, analytical, clinical development,
and device manufacturing capabilities. The Sofusa platform is a
novel microneedle technology that delivers both small and large
molecule drugs through the skin and into the initial lymphatic
capillaries resulting in significantly higher drug concentrations
in lymph nodes over sustained periods of time compared to
traditional injections or infusions. Drug targets for many diseases
of the immune system (e.g., autoimmune diseases and cancer) reside
in the lymphatic system and lymph nodes. In multiple pre-clinical
models, Sofusa’s proprietary nanotopography-draped microneedle
system has consistently demonstrated the ability to improve
therapeutic responses by delivering over 40-fold increases in drug
concentration to targeted lymph nodes when compared to traditional
subcutaneous injections or intravenous infusions. The Sofusa
Business Unit is currently conducting human proof of concept
studies in autoimmune disease and in cancer.
About Sorrento Therapeutics, Inc.
Sorrento is a clinical and commercial stage biopharmaceutical
company developing new therapies to treat cancer, pain (non-opioid
treatments), autoimmune disease and COVID-19. Sorrento's
multimodal, multipronged approach to fighting cancer is made
possible by its extensive immunooncology platforms, including key
assets such as next-generation tyrosine kinase inhibitors (“TKIs”),
fully human antibodies (“G-MAB™ library”), immuno-cellular
therapies (“DAR-T™”), antibody-drug conjugates (“ADCs”), and
oncolytic virus (“Seprehvec™”). Sorrento is also developing
potential antiviral therapies and vaccines against coronaviruses,
including STI-1558, Abivertinib, COVISHIELD™ and COVIDROPS™; and
diagnostic test solutions, including COVIMARK™.
Sorrento's commitment to life-enhancing therapies for patients
is also demonstrated by our effort to advance a (TRPV1 agonist)
non-opioid pain management small molecule, resiniferatoxin (“RTX”),
and SP-102 (10 mg, dexamethasone sodium phosphate viscous gel)
(SEMDEXA™), a novel, viscous gel formulation of a widely used
corticosteroid for epidural injections to treat lumbosacral
radicular pain, or sciatica, and to commercialize ZTlido®
(lidocaine topical system) 1.8% for the treatment of postherpetic
neuralgia (PHN). RTX has been cleared for a Phase II trial for
intractable pain associated with cancer and a Phase II trial in
osteoarthritis patients. Positive final results from the Phase III
Pivotal Trial C.L.E.A.R. Program for SEMDEXA™, its novel,
non-opioid product for the treatment of lumbosacral radicular pain
(sciatica), were announced in March 2022. ZTlido® was approved by
the FDA on February 28, 2018. For more information visit
www.sorrentotherapeutics.com
Forward Looking Statements
This press release and any statements made for and during any
presentation or meeting contain forward-looking statements related
to Sorrento Therapeutics, Inc., under the safe harbor provisions of
Section 21E of the Private Securities Litigation Reform Act of 1995
and subject to risks and uncertainties that could cause actual
results to differ materially from those projected. Forward-looking
statements include statements regarding the expectations for
Sorrento's and its subsidiaries' technologies and product
candidates, including clinical trial results. Risks and
uncertainties that could cause our actual results to differ
materially and adversely from those expressed in our
forward-looking statements, include, but are not limited to: risks
related to Sorrento's and its subsidiaries', affiliates’ and
partners’ technologies and prospects and collaborations with
partners; risks related to seeking regulatory approvals and
conducting clinical trials; risks related to leveraging the
expertise of its employees, subsidiaries, affiliates and partners
to assist Sorrento in the execution of its product candidates’
strategies; risks related to the global impact of COVID-19; and
other risks that are described in Sorrento's most recent periodic
reports filed with the Securities and Exchange Commission,
including Sorrento's Annual Report on Form 10-K for the year ended
December 31, 2021, and subsequent Quarterly Reports on Form 10-Q
filed with the Securities and Exchange Commission, 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 we undertake
no obligation to update any forward-looking statement in this press
release except as required by law.
Media and Investor Relations
Contact: Brian Cooley Email:
mediarelations@sorrentotherapeutics.com
Sorrento® and the Sorrento logo are registered trademarks of
Sorrento Therapeutics, Inc. G-MAB™, DAR-T™, Seprehvec™, SOFUSA™,
COVISHIELD™, COVIDROPS™, COVI-MSC™, COVIMARK™ and Fujovee™ are
trademarks of Sorrento Therapeutics, Inc. SEMDEXA™ (SP-102) is a
trademark of Semnur Pharmaceuticals, Inc. A proprietary name review
by the FDA is planned. ZTlido® is a registered trademark owned by
Scilex Pharmaceuticals Inc. All other trademarks are the property
of their respective owners. ©2022 Sorrento Therapeutics, Inc. All
Rights Reserved.
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