Genprex to Participate at the Diamond Equity Research Emerging Growth Invitational on December 1
November 24 2020 - 8:16AM
Business Wire
Presentation to Highlight the Promise of Novel
Gene Therapies to Transform Cancer and Diabetes Treatments
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 participate at the Diamond
Equity Research Emerging Growth Invitational taking place virtually
on December 1, 2020. Genprex’s Executive Vice President and Chief
Operating Officer, Michael Redman, will virtually deliver a company
overview to investors followed by a guided question and answer
session.
Event: Diamond Equity Research Emerging Growth
Invitational Date: Tuesday, December 1 Time: 11:40
a.m. EST Registration Link: https://bit.ly/2UJS3Si
A live audio webcast and archive of the conference presentation
will be available for a period of time using the registration link
above. For more information on the Diamond Equity Research Emerging
Growth Invitational, please contact your Diamond Equity Research
representative.
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 and planned clinical trials, 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 FDA approval of REQORSA and our other
potential product candidates including whether we receive 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/20201124005208/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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