drugset / Trial / NCT04472494

Study of Abatacept in the Treatment of Hospitalized COVID-19 Participants With Respiratory Compromise

NCT04472494 ↗

Phase 2 Terminated 61 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of intravenous abatacept administered to hospitalized COVID-19 participants with respiratory compromise.

Timeline

Start
2020-10-14
Primary completion
2021-08-12
Completion
2021-09-13

Outcome

Missed primary endpoint

Stopped (Enrollment): “Slow accrual”

registry analysis (superiority test); Abatacept vs Placebo; p = 0.9297; Odds Ratio (OR) 1.07 (95% CI 0.26 to 4.49); NCT04472494 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Abatacept Other / unclassified — Intravenous

Indications