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

Study results available
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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

Placebo

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
  • Medical Research Council

    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
  • Pfizer

    collaborator INDUSTRY
  • University of Minnesota

    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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05780541 on ClinicalTrials.gov