Tetra Bio-Pharma and Cellvera have entered an agreement to jointly develop ARDS-003 as an oral combination therapeutic candidate with 400mg Qifenda (Favipiravir) for Covid-19.
A first-in-human drug product, ARDS-003 contains the active pharmaceutical agent, Onternabez.
Onternabez is a selective full agonist of the type 2 cannabinoid receptor (CB2R).
ARDS-003, in preclinical studies, was found to lower the hyperinflammatory response and decelerate the progression of the disease.
In the humanised ACE2 mouse model, ARDS-003 monotherapy showed to lower morbidity and mortality signs, including respiratory distress after Covid-19 in a dose-dependent manner, versus placebo.
It is claimed to have outperformed an antiviral drug in lowering various proinflammatory mediators linked to hyperinflammation and dysfunction of the immune system after viral infection.
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By GlobalDataQifenda is a broad-spectrum antiviral drug in the commercial stage.
Developed by FujiFilm Toyama Chemical, Favipiravir is currently owned by Cellvera.
A selective viral RNA-dependent RNA polymerase (RdRP) inhibitor, Favipiravir has antiviral activity against single-stranded RNA viruses, such as coronaviruses.
Based on findings from Prepaire, an artificial intelligence (AI)-based in-silico drug discovery platform, the companies estimate the Favipiravir plus ARDS-003 combination could aid in the quick clearance of virus and offer lasting benefits.
Additionally, the cytokine lowering properties of ARDS-003 may avert some consequences of Covid-19, such as severe pulmonary inflammation.
Tetra Bio-Pharma CEO and CRO Guy Chamberland said: “This partnership with a pharmaceutical company with global reach is a sign of the potential for the ARDS-003 drug asset.
“We look forward to working jointly with Cellvera to bring this combination drug product forward to improve treatment options for patients worldwide.”