Clinical-stage gene therapy company Genprex, Inc. (NASDAQ:GNPX) announced on Wednesday that it has secured an exclusive worldwide license from the University of Michigan for its lead drug candidate, Reqorsa Gene Therapy (quaratusugene ozeplasmid).
This agreement allows Genprex to develop Reqorsa in combination with ALK inhibitors for treating ALK-EML4 positive translocated lung cancer. Reqorsa targets the TUSC2 gene, a tumour suppressor often deleted in lung cancer and could offer a new approach for patients with ALK+ non-small cell lung cancer (NSCLC).
Preclinical data presented at the 2024 American Association for Cancer Research (AACR) Annual Meeting showed Reqorsa induced apoptosis in alectinib-resistant EML4-ALK positive NSCLC cell lines. The results suggest that REQORSA could effectively reduce cell growth and proliferation in these cancer cells by activating apoptotic pathways. Genprex views these findings as a foundation for further clinical investigation of Reqorsa in treating ALK+ NSCLC.
Reqorsa utilizes Genprex's ONCOPREX Delivery System, encapsulating the TUSC2 gene in lipid-based nanoparticles to specifically target cancer cells. This non-viral, electrically charged formulation enhances the delivery of TUSC2 to cancer cells while minimizing normal tissue uptake. Genprex aims to develop Reqorsa in combination with existing therapies, positioning it as a potentially improved treatment for NSCLC, SCLC and other cancers.
Neurizon Therapeutics reports breakthrough preclinical results for ALS treatment candidate NUZ-001
Cytokinetics and Bayer partner on aficamten for Japanese HCM patients
Nektar Therapeutics announces 2024 ACR conference oral presentation of NKTR-422 preclinical data
GRAIL reports first patient tested with blood-based assay in TROPION-Lung12 Phase 3 study
SK Biopharmaceuticals enters radiopharmaceutical therapy research agreement
Adicet Bio doses first patient in Phase 1 trial of ADI-001 for lupus nephritis
Cybin's CYB003 shows 12-month efficacy in Phase 2 MDD trial
Scancell reports promising SCOPE trial data for SCIB1 in advanced melanoma
AstraZeneca's Tagrisso Recommended for EU approval for unresectable EGFR-mutated lung cancer
Martin Pharmaceuticals announces DREAM study results at 75th Annual Liver Meeting of AASLD
Rona Therapeutics reveals positive outcome from RN0191 phase one clinical trial
Merck's KEYTRUDA plus chemotherapy receives positive EU opinion for first-line MPM treatment
Sanofi seeks FDA approval for Dupixent in chronic spontaneous urticaria