Licensed technologies include use of Genprex’s TUSC2 gene therapy combined with immunotherapy drugs, including:
- Pembrolizumab (Merck’s largest selling drug Keytruda®)
- Nivolumab (Bristol-Myers Squibb’s Opdivo®)
- Ipilimumab (Bristol-Myers Squibb’s Yervoy®)
Genprex, Inc. (“Genprex” or the “Company”) (Nasdaq:
GNPX),
a clinical-stage gene therapy company developing potentially
life-changing technologies for patients with cancer and diabetes, today
announced that it has entered into a Patent and Technology License
Agreement (“License Agreement”) with The University of Texas MD Anderson
Cancer Center (“MD Anderson”) in which MD Anderson granted to Genprex
an exclusive worldwide license to a portfolio of 16 patent applications
and related technology (“Licensed IP”) for the treatment of cancer using
Genprex’s lead drug candidate and TUSC2 gene therapy, known as
“Oncoprex” or “GEN-001,” in combination with immunotherapies. This is a
distinct therapeutic approach from that of combining Oncoprex with
targeted therapies such as osimertinib (marketed as Tagrisso® by
AstraZeneca).
Genprex was recently awarded U.S. FDA Fast Track designation for use
of Oncoprex combined with Tagrisso for the treatment of non-small cell
lung cancer (NSCLC) patients with EGFR mutations whose tumors progressed
after treatment with Tagrisso alone. The Company is now preparing to
file an Investigational New Drug application to initiate a clinical
trial of Oncoprex in combination with pembrolizumab (marketed as
Keytruda® by Merck) in NSCLC.
https://www.businesswire.com/news/home/20200505005133/en/Genprex-Enters-Exclusive-Worldwide-Patent-Technology-License
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