Genprex to Present its Cutting-Edge Gene Therapies at the MoneyShow Accredited Investors Virtual Expo
January 21 2021 - 8:30AM
Business Wire
Presentation to Highlight Company’s Recent
Advancements on its Upcoming Clinical Trials for the Treatment of
Non-Small Cell Lung Cancer
Genprex, Inc. (“Genprex” or the “Company”)
(NASDAQ: GNPX), a clinical-stage gene therapy company focused on
developing life-changing therapies for patients with cancer and
diabetes, today announced that the Company will present at the
MoneyShow Accredited Investors Virtual Expo taking place virtually
January 26-28, 2021. Genprex’s President and Chief Executive
Officer, Rodney Varner, will virtually deliver a company overview,
including recent progress made on its upcoming clinical trials, to
participating investors on Thursday, January 28.
Event: MoneyShow Accredited Investors Virtual Expo
Presentation Date: Thursday, January 28 Presentation
Time: 12:25 p.m. EST Registration Link:
http://bit.ly/3p0yJOl
The presentation will be available for replay on the Company's
website (www.genprex.com) for a period of time following the
conference, and the video will be archived on MoneyShow.com.
About Genprex, Inc.
Genprex, Inc. is a clinical-stage gene therapy company focused
on developing life-changing therapies for patients with cancer and
diabetes. Genprex’s technologies are designed to administer
disease-fighting genes to provide new therapies for large patient
populations with cancer and diabetes who currently have limited
treatment options. Genprex works with world-class institutions and
collaborators to develop drug candidates to further its pipeline of
gene therapies in order to provide novel treatment approaches. The
Company’s lead product candidate, REQORSA™ (quaratusugene
ozeplasmid), is being evaluated as a treatment for non-small cell
lung cancer (NSCLC). REQORSA has a multimodal mechanism of action
that has been shown to interrupt cell signaling pathways that cause
replication and proliferation of cancer cells; re-establish
pathways for apoptosis, or programmed cell death, in cancer cells;
and modulate the immune response against cancer cells. REQORSA has
also been shown to block mechanisms that create drug resistance. In
January 2020, the U.S. Food and Drug Administration granted Fast
Track Designation for REQORSA for NSCLC in combination therapy with
osimertinib (AstraZeneca’s Tagrisso®) for patients with EFGR
mutations whose tumors progressed after treatment with osimertinib
alone.
For more information, please visit the Company’s web site at
www.genprex.com or follow Genprex on Twitter, Facebook and
LinkedIn.
Forward-Looking Statements
Statements contained in this press release regarding matters
that are not historical facts are "forward-looking statements"
within the meaning of the Private Securities Litigation Reform Act
of 1995. Because such statements are subject to risks and
uncertainties, actual results may differ materially from those
expressed or implied by such forward-looking statements. Such
statements include, but are not limited to, statements regarding
the effect of Genprex’s product candidates, alone and in
combination with other therapies, on cancer and diabetes, regarding
potential, current, regarding the Company’s future growth and
financial status and regarding our commercial partnerships and
intellectual property licenses. Risks that contribute to the
uncertain nature of the forward-looking statements include the
presence and level of the effect of our product candidates, alone
and in combination with other therapies, on cancer; the timing and
success of our clinical trials and planned clinical trials of
REQORSA™ immunogene therapy drug, alone and in combination with
targeted therapies and/or immunotherapies, and whether our other
potential product candidates, including GPX-002, our gene therapy
in diabetes, advance into clinical trials; the success of our
strategic partnerships, including those relating to manufacturing
of our product candidates; the timing and success at all of
obtaining any FDA approvals of REQORSA and our other potential
product candidates including whether we receive necessary approvals
to commence clinical trials or benefit from fast track or similar
regulatory designations; costs associated with developing our
product candidates, whether we identify and succeed in acquiring
other technologies and whether patents will ever be issued under
patent applications that are the subject of our license agreements
or otherwise. These and other risks and uncertainties are described
more fully under the caption “Risk Factors” and elsewhere in our
filings and reports with the United States Securities and Exchange
Commission. All forward-looking statements contained in this press
release speak only as of the date on which they were made. We
undertake no obligation to update such statements to reflect events
that occur or circumstances that exist after the date on which they
were made.
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version on businesswire.com: https://www.businesswire.com/news/home/20210121005223/en/
Genprex, Inc. (877) 774-GNPX (4679) Investor
Relations GNPX Investor Relations (877) 774-GNPX (4679) ext. #2
investors@genprex.com Media Contact Genprex Media Relations
Kalyn Dabbs (877) 774-GNPX (4679) ext. #3 media@genprex.com
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