Clinical-stage biopharmaceutical company Vistagen (Nasdaq:VTGN) announced on Wednesday that it has received a US patent for AV-101, its oral non-opioid candidate for neuropathic pain.
The patent extends until at least 2034 and is part of the company's global intellectual property portfolio on AV-101's therapeutic applications.
Preclinical research published in The Journal of Pain demonstrated AV-101's antinociceptive effects comparable to gabapentin, but with a more favourable side effect profile. Additional studies using the Chung ligation model showed that AV-101 had a significant dose response, with efficacy similar to pregabalin.
Phase 1 clinical studies, published in the Scandinavian Journal of Pain, indicated AV-101 was well-tolerated, with no significant differences in adverse events compared to placebo. Though not designed for statistical significance, the study showed reductions in allodynia pain and hyperalgesia.
Vistagen plans to explore strategic collaborations to advance AV-101's clinical development and commercialisation for NMDA receptor-related disorders, particularly in pain management.
Akeso agrees clinical trial collaboration with INOVIO
Airiver Medical's Airiver Pulmonary DCB receives US FDA Breakthrough Device Designation
Frontage Laboratories acquires Teddy Clinical Research Laboratory in China
Allergy Therapeutics reports positive biomarker data from PROTECT trial
HUTCHMED doses first patient in global trial of ATTC candidate HMPL-A580
Ensorcell adds new senior leadership team members
Sino Biological launches 2026-2027 Northern Hemisphere influenza vaccine strain antigens
Sanaregen receives FDA clearance for retinal degeneration clinical trial
Lynk Pharmaceuticals reveals positive topline results from zemprocitinib Phase III clinical trial
ReviR Therapeutics doses first participant in First-in-Human Phase 1 clinical trial of RTX-117
Ono Pharmaceutical expands multi-target research collaboration with Congruence Therapeutics
United Therapeutics' ralinepag reduces risk of clinical worsening in pivotal PAH study
Genentech's fenebrutinib meets primary endpoint in pivotal Phase III study for multiple sclerosis
ValiRx establishes animal health subsidiary to target veterinary oncology market
FDA accepts rusfertide NDA and grants priority review for polycythemia vera