Clinical trial
AN INTERVENTIONAL EFFICACY AND SAFETY, PHASE 2/3, DOUBLE-BLIND, 2-ARM STUDY TO INVESTIGATE ORALLY ADMINISTERED PF-07321332/RITONAVIR COMPARED WITH PLACEBO IN NONHOSPITALIZED SYMPTOMATIC ADULT PARTICIPANTS WITH COVID-19 WHO ARE AT INCREASED RISK OF PROGRESSING TO SEVERE ILLNESS
NCT04960202 is registered in ClinicalTrials.gov with Pfizer as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- AN INTERVENTIONAL EFFICACY AND SAFETY, PHASE 2/3, DOUBLE-BLIND, 2-ARM STUDY TO INVESTIGATE ORALLY ADMINISTERED PF-07321332/RITONAVIR COMPARED WITH PLACEBO IN NONHOSPITALIZED SYMPTOMATIC ADULT PARTICIPANTS WITH COVID-19 WHO ARE AT INCREASED RISK OF PROGRESSING TO SEVERE ILLNESS
- Lead sponsor
- Pfizer
- Phase
- Phase 2/3
- Overall status
- Completed
- Start date
- July 16, 2021
- Completion date
- April 25, 2022
- Enrollment
- 2,091 (actual)
- Sites
- 201
Conditions
As the registry lists them; a condition with its own page is linked.