Peptides and proteins company Relief Therapeutics Holdings AG (SIX:RLF)(OTC:RLFTF) said on Thursday that NeuroRx Inc has received the Investigational New Drug (IND) permission to test RLF-100 (aviptadil) for inhaled use in patients with moderate and severe COVID-19.
The company added that the clinical trial of the inhaled formulation of RLF-100 is expected to begin on or before 1 September 2020. The first phase will commence with patients hospitalized for severe COVID-19 who do not yet have respiratory failure and the trial will expand to patients at home with mild and moderate COVID-19 in order to prevent the need for hospital admission.
According to the company, RLF-100 (aviptadil) is a patented formulation of Vasoactive Intestinal Polypeptide (VIP), which is highly concentrated in the lungs and inhibits a variety of inflammatory cytokines.
COVID-19-related death is primarily caused by respiratory failure, but there is evidence of early viral infection of the alveolar type 2 cells. Injury to the type 2 alveolar cells is an increasingly plausible mechanism of COVID-19 disease progression (Mason 2020). These specialized cells replenish the more common type 1 cells that line the lungs, concluded the company.
Tyra Biosciences doses first patient in TYRA-300 Phase 2 study for bladder cancer
argenx advances ARGX-119 to registrational study for congenital myasthenic syndromes
hVIVO supports Cidara Therapeutics' positive Phase 2b influenza study results
Sanofi's riliprubart receives orphan drug designation in Japan for CIDP
HUTCHMED gains China approval for ORPATHYS and TAGRISSO combination in lung cancer
Hikma Pharmaceuticals USA announces USD1bn of new US investment
UCB reports positive Phase 3 results for fenfluramine in CDKL5 deficiency disorder