Genelux Corporation Receives FDA Fast Track Designation for Olvi-Vec in Platinum Resistant/Refractory Ovarian Cancer
27 Novembro 2023 - 9:00AM
Genelux Corporation (NASDAQ: GNLX), a late clinical-stage
immuno-oncology company, today announced that the United States
Food and Drug Administration (FDA) has granted Fast Track
designation for the development program of Olvi-Vec (olvimulogene
nanivacirepvec) for the treatment of patients with platinum
resistant/refractory ovarian cancer.
“The Fast Track designation granted for Olvi-Vec
underscores its potential to address unmet medical needs in ovarian
cancer, a significant recognition as we continue to enroll our
Phase 3 OnPrime study,” said Thomas Zindrick, President, Chairman
and CEO of Genelux. “We eagerly anticipate ongoing engagement with
the FDA as we progress in the development of this promising
treatment.”
Genelux is currently conducting
OnPrime/GOG-3076, a Phase 3 multi-center, randomized, open-label
registrational trial evaluating the efficacy and safety of Olvi-Vec
in combination with platinum-based chemotherapy in patients with
platinum-resistant/refractory ovarian cancer. More information
about the trial is accessible at www.ClinicalTrials.gov, identifier
NCT05281471.
The purpose of Fast Track designation is to
facilitate the development and hasten the review process of drugs
aimed at treating serious and life-threatening conditions, ensuring
that an approved product can swiftly enter the market. Notable
aspects of Fast Track designation encompass regular engagements
with the FDA review team, and, if specific criteria are satisfied,
potential eligibility for Priority Review and Rolling Review.
About Genelux
CorporationGenelux is a late clinical-stage
biopharmaceutical company focused on developing a pipeline of
next-generation oncolytic immunotherapies for patients suffering
from aggressive and/or difficult-to-treat solid tumor types. The
Company's most advanced product candidate, Olvi-Vec (olvimulogene
nanivacirepvec), is a proprietary, modified strain of the vaccinia
virus. Olvi-Vec currently is being evaluated in OnPrime/GOG-3076, a
multi-center, randomized, open-label Phase 3 registrational trial
evaluating the efficacy and safety of Olvi-Vec in combination with
platinum-doublet + bevacizumab compared to platinum-doublet +
bevacizumab in patients with platinum-resistant/refractory ovarian
cancer. The core of Genelux' discovery and development efforts
revolves around the company's proprietary CHOICE™ platform from
which the Company has developed an extensive library of isolated
and engineered oncolytic vaccinia virus immunotherapeutic product
candidates, including Olvi-Vec. For more information, please visit
www.genelux.com and follow us on Twitter @Genelux_Corp and on
LinkedIn.
Forward-Looking StatementsThis
release contains “forward-looking statements” within the meaning of
Section 27A of the Securities Act of 1933, as amended, and Section
21E of the Securities Exchange Act of 1934, as amended, and such
forward-looking statements are made pursuant to the safe harbor
provisions of the Private Securities Litigation Reform Act of 1995.
“Forward-looking statements” describe future expectations, plans,
results, or strategies and are generally preceded by words such as
“believes,” “anticipates,” “expect,” “may,” “plan” or “will”.
Forward-looking statements in this release include, but are not
limited to, statements related to Genelux’s future, the execution
of its corporate strategy and operating plan, clinical trials for
Olvi-Vec and their potential success, and Olvi-Vec’s potential to
address unmet medical needs in ovarian cancer. Such statements are
subject to a multitude of risks and uncertainties that could cause
future circumstances, events, or results to differ materially from
those projected in the forward-looking statements. These and other
risks are identified under the caption “Risk Factors” in Genelux’
filings with the Securities and Exchange Commission. All
forward-looking statements contained in this press release speak
only as of the date on which they were made and are based on
management’s assumptions and estimates as of such date. Genelux
does not undertake any obligation to publicly update any
forward-looking statements, whether as a result of the receipt of
new information, the occurrence of future events or otherwise.
Investor and Media Contacts
Ankit Bhargava, MDAllele Communications,
LLCgenelux@allelecomms.com
Source: Genelux Corporation
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