Your session is about to expire
← Back to Search
mTOR inhibitor
Sirolimus for Coronavirus (SCOPE Trial)
Phase 2
Waitlist Available
Led By Nishant Gupta, MD
Research Sponsored by University of Cincinnati
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 28 days
Awards & highlights
SCOPE Trial Summary
This trial is testing whether the drug sirolimus can help improve outcomes for people hospitalized with COVID-19. 30 people will be randomly assigned to either receive sirolimus or a placebo, and will be monitored for changes in their condition.
Eligible Conditions
- Coronavirus
- COVID-19
SCOPE Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 28 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~28 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Percentage of Patients Who Are Alive and Free From Advanced Respiratory Support Measures at Day 28.
Secondary outcome measures
Drug Safety Profile
Duration of Hospital Stay
Number of Patients Who Require Initiation of Off-label Therapies
+1 moreSCOPE Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: SirolimusActive Control1 Intervention
Sirolimus 6mg on day 1 followed by 2mg daily for the next 13 days or until hospital discharge, whatever happens sooner.
Group II: PlaceboPlacebo Group1 Intervention
Matching placebo
Find a Location
Who is running the clinical trial?
University of CincinnatiLead Sponsor
428 Previous Clinical Trials
634,362 Total Patients Enrolled
Nishant Gupta, MD5.02 ReviewsPrincipal Investigator - University of Cincinnati
University of Cincinnati
2 Previous Clinical Trials
129 Total Patients Enrolled
5Patient Review
This professional was terrific. They had excellent knowledge and provided terrific explanations.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Share this study with friends
Copy Link
Messenger