Genprex Receives Safety Review Committee Approval to Advance to Highest Dose Group in Phase 1 Portion of Acclaim-3 Clinical Trial of Reqorsa® Gene Therapy in Combination with Tecentriq® in...
Genprex, Inc. (GNPX)
Last genprex, inc. earnings: 11/14 12:08 pm
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Source: Yahoo! Finance
AUSTIN, Texas Oct. 15, 2024 /PRNewswire/ -- Genprex, Inc. ("Genprex" or the "Company") (NASDAQ: ), a clinical-stage gene therapy company focused on developing life-changing therapies for patients with cancer and diabetes, today announced that it has completed the 0.09 mg/kg dose group of the Phase 1 dose escalation portion of the Acclaim-3 clinical trial of Reqorsa ® Gene Therapy (quaratusugene ozeplasmid) in combination with Tecentriq ® (atezolizumab) as maintenance therapy for patients with extensive stage small cell lung cancer (ES-SCLC). In addition, the Safety Review Committee (SRC) has approved escalation to the highest dose group of 0.12 mg/kg. The combination of REQORSA and atezolizumab previously received U.S. Food and Drug Administration's (FDA) Fast Track Designation for the treatment of the Acclaim-3 patient population and the FDA has also granted Orphan Drug Designation to REQORSA for the treatment of SCLC. "We believe the SRC's recommendation to advance to the highest
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News
- Genprex Signs Exclusive License to Additional Gene Therapy Technologies with the University of Michigan for the Treatment of Lung Cancer [Yahoo! Finance]Yahoo! Finance
- Genprex Signs Exclusive License to Additional Gene Therapy Technologies with the University of Michigan for the Treatment of Lung CancerPR Newswire
- Genprex Collaborators Present Positive Preclinical Data on Reqorsa® Gene Therapy at the Society for Immunotherapy of Cancer 2024 Annual MeetingPR Newswire
- Genprex to Participate in 2024 BIO Europe Conference [Yahoo! Finance]Yahoo! Finance
- Genprex to Participate in 2024 BIO Europe ConferencePR Newswire
GNPX
Sec Filings
- 11/20/24 - Form 8-K
- 11/19/24 - Form 8-K
- 11/13/24 - Form 10-Q
- GNPX's page on the SEC website