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NNRTI
Doravirine for Human Immunodeficiency Virus Infection
Phase 4
Waitlist Available
Research Sponsored by Clinique du Quartier Latin
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 24 weeks
Awards & highlights
Study Summary
This trial will test the safety and efficacy of switching from the drug etravirine to doravirine in patients with resistance to multiple HIV medications who are also taking other ARV drugs. The other ARV drugs (protease inhibitor, entry inhibitor and integrase inhibitor) will not be changed. The trial will be performed at only two sites.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Percentage of subjects who maintain virologic control .
Side effects data
From 2020 Phase 3 trial • 15 Patients • NCT040794527%
Diarrhea
7%
Thoracic pain
100%
80%
60%
40%
20%
0%
Study treatment Arm
Doravirine+TAF/FTC Arm (Single Arm)
Trial Design
1Treatment groups
Experimental Treatment
Group I: switch from etravirine to doravirineExperimental Treatment1 Intervention
switches to doravirine,
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Etravirine
FDA approved
Find a Location
Who is running the clinical trial?
Clinique du Quartier LatinLead Sponsor
Merck Frosst Canada Ltd.Industry Sponsor
29 Previous Clinical Trials
12,367 Total Patients Enrolled
Frequently Asked Questions
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