The Prevent Severe COVID-19 (PRESECO) Study

NCT04600895 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 1187

Last updated 2024-03-29

Study results available
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Summary

Double-blinded, placebo control, randomized, phase-3 clinical trial to evaluate clinical efficacy of Favipiravir in patients with mild to moderate symptoms related to COVID-19 infection

Conditions

  • Covid19

Interventions

DRUG

Favipiravir

Favipiravir

DRUG

Placebo

Placebo

Sponsors & Collaborators

  • Appili Therapeutics Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-11-30
Primary Completion
2021-10-20
Completion
2021-10-20
FDA Drug
Yes

Countries

  • United States
  • Brazil
  • Mexico

Study Locations

More Related Trials

Entities

Drugs

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 NCT04600895 on ClinicalTrials.gov