drugset / Trial / NCT04472728

Testing the Efficacy and Safety of BIO101 for the Prevention of Respiratory Deterioration in COVID-19 Patients

NCT04472728

Phase 2/3 Terminated 238 enrolled Biophytis
RandomizedSequentialQuadruple-blindTreatment

Summary

The COVA clinical study is a global multicentric, double-blind, placebo-controlled, group sequential and adaptive 2 parts phase 2-3 study targeting in patients with SARS-CoV-2 pneumonia. Part 1 is a Phase 2 exploratory Proof of Concept (PoC) study to provide preliminary data on the activity, safety and tolerability of BIO101 in the target population. Part 2 is a phase 3 pivotal randomized study to provide further evidence of safety and efficacy of BIO101 after 28 days of double-blind dosing. BIO101 is the investigational new drug that activates the Mas receptor (MasR) through the protective arm of the Renin Angiotensin System (RAS).

Timeline

Start
2020-08-26
Primary completion
2022-06-06
Completion
2022-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject 20-hydroxyecdysone Small molecule 350 mg Oral

Indications