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Wednesday, July 29, 2020

Relief Therapeutics’s Aviptadil gets FDA expanded access protocol for COVID-19

FDA signs off expanded access protocol to Relief Therapeutics’s (OTCPK:RLFTF) and its U.S. partner NeuroRx, for RLF-100 (aviptadil) in COVID-19 patients with respiratory failure.
The protocol makes treatment available to patients who have exhausted approved therapies and are not eligible for the current phase 2/3 trial of RLF-100 because of other medical conditions.
RLF-100 is a patented formulation of Aviptadil (synthetic human Vasoactive Intestinal Polypeptide VIP), which inhibits pro-inflammatory cytokines and protects alveolar type 2 cells in the lungs inhibiting pro-inflammatory cytokines, essential for oxygen exchange.

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