Emetine for Viral Outbreaks: Randomized, Double-Blind, Placebo-Controlled, Clinical Trial to Evaluate Oral Emetine Against Covid-19 (EVOLVE)

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

The goal of this clinical trial (phase 2/phase 3) is to evaluate the efficacy and safety of emetine administered orally for symptomatic Covid-19 patients in patients ages 30 years and above. Participants will be asked to: * Take Emetine 6mg orally for 10 consecutive days * Be monitored by healthcare staff or self-monitor for daily vital signs and symptoms * Undergo blood draws Researchers will compare the control group given placebo medicine to assess if emetine improved the symptoms of Covid-19.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 30
Healthy Volunteers: f
View:

• 30 years of age or older at time of randomization

• RT-PCR positive for SARS-CoV-2 infection within ≤ 10 days of the screening visit.

• In addition to confirmed RT-PCR, symptomatic Covid-19 patients with at least two or more symptoms within 7 days of the screening visit: Cough, shortness of breath, fever/chills, sore throat, nausea, vomiting, diarrhea, fatigue, body aches, headache

• Ability to give informed consent (administered in local language)

Locations
United States
Maryland
Johns Hopkins University, Division of Infectious Diseases
NOT_YET_RECRUITING
Baltimore
Other Locations
Nepal
Bharatpur Hospital
RECRUITING
Bharatpur
Contact Information
Primary
Kunchok Dorjee, MBBS, PhD
kdorjee1@jhmi.edu
4105027135
Time Frame
Start Date: 2024-05-15
Estimated Completion Date: 2026-09-14
Participants
Target number of participants: 600
Treatments
Active_comparator: Emetine
Participant takes Emetine 6mg for 10 consecutive days
Placebo_comparator: Placebo
Participant takes a placebo for 10 consecutive days
Related Therapeutic Areas
Sponsors
Collaborators: Nepal Health Research Council, Rutgers University, Bharatpur Hospital Chitwan, Stony Brook University
Leads: Johns Hopkins University

This content was sourced from clinicaltrials.gov