Name (Synonyms) | Correlation | |
---|---|---|
drug2148 | SBI-101 Wiki | 1.00 |
drug1822 | Placebo Wiki | 0.06 |
There is one clinical trial.
The objectives of this study are to evaluate the safety, tolerability and efficacy of AT-527 in older subjects (ages 45-80 years) with moderate COVID-19 and risk factors for poor outcomes (such as obesity (BMI>30), hypertension, diabetes or asthma). Eligible subjects will be randomized to blinded AT-527 (nucleotide analog) tablets or matching placebo tablets to be administered orally for 5 days. Local supportive standard of care (SOC) will be allowed for all subjects. Efficacy and safety observations will be compared for treatment with active AT-527 tablets + SOC vs. placebo tablets + SOC.
Description: Progressive respiratory insufficiency defined as a ≥ 2-tier increase in respiratory support methods required to maintain satisfactory oxygenation (SpO2 ≥ 93%), using the 6-tier hierarchical scale of respiratory support methods
Measure: Proportions (active vs. placebo) of subjects with progressive respiratory insufficiency. Time: Day 14Description: Clinical recovery defined as time from randomization to disease resolution status on an 8 point Clinical Status scale
Measure: Time to clinical recovery Time: Day 14