PF-07304814 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial)
NCT05780541 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 58
Last updated 2024-02-09
Summary
This study looks at the safety and effectiveness of PF-07304814 in treating COVID-19 in people who have been hospitalized with the infection. Participants in the study will be treated with either PF-07304814 plus current standard of care (SOC), or with placebo plus current SOC. This is ACTIV-3/TICO Treatment Trial H6.
Conditions
Interventions
- DRUG
-
PF-07304814
PF-07304814 is a phosphate ester prodrug of PF-00835231 (active moiety), a potent and selective inhibitor of the SARS-CoV-2 3CLpro.
- DRUG
-
Commercially available 0.9% sodium chloride solution
- BIOLOGICAL
-
Remdesivir
Antiviral agent
Sponsors & Collaborators
-
International Network for Strategic Initiatives in Global HIV Trials (INSIGHT)
collaborator NETWORK -
University of Copenhagen
collaborator OTHER - collaborator OTHER_GOV
-
Kirby Institute
collaborator OTHER_GOV -
Washington D.C. Veterans Affairs Medical Center
collaborator FED -
Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
collaborator NETWORK -
National Heart, Lung, and Blood Institute (NHLBI)
collaborator NIH -
US Department of Veterans Affairs
collaborator FED -
Prevention and Early Treatment of Acute Lung Injury
collaborator OTHER -
Cardiothoracic Surgical Trials Network
collaborator OTHER - collaborator INDUSTRY
- collaborator OTHER
-
National Institute of Allergy and Infectious Diseases (NIAID)
lead NIH
Principal Investigators
-
Jens Lundgren, Prof. · INSIGHT Copenhagen International Coordinating Centre, Rigshospitalet, University of Copenhagen
-
James Neaton, Prof. · INSIGHT Statistical and Data Management Center, University of Minnesota
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-09-15
- Primary Completion
- 2022-04-06
- Completion
- 2023-07-14
- FDA Drug
- Yes
Countries
- United States
- Denmark
Study Locations
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