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Find Clinical Drug Pipeline Developments & Deals for TERN-201
Part 1 of AVIATION Trial met primary safety endpoint compared to placebo, for TERN-201, a highly selective, irreversible, covalent inhibitor of VAP-1, administered for 12 weeks to presumed NASH patients was generally well-tolerated with a similar incidence of adverse events.
The trial will evaluate the safety, pharmacokinetics, pharmacodynamics, and efficacy of TERN-201 in patients with presumed non-cirrhotic NASH and a cT1 value of greater than 800ms.
Terns recently completed a Phase 1 clinical study of TERN-201, which demonstrated that single and multiple oral administrations of TERN-201 were well tolerated with no significant safety findings observed.
Results from single and multiple ascending dose cohorts demonstrate TERN-201 is generally safe and well tolerated and results in potent and sustained inhibition of plasma SSAO activity.
The company will give an oral presentation reviewing Phase 1 data on TERN-201, its semicarbazide-sensitive amine oxidase (SSAO) inhibitor in development for NASH.