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Anti-viral
Treatment Arm for Chronic Hepatitis C
Phase 4
Waitlist Available
Research Sponsored by Peter J. Ruane, M.D., Inc.
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 sustained virologic response 12 weeks after treatment completion
Awards & highlights
Study Summary
This study is evaluating the safety and efficacy of a 12 week treatment LDV/SOF FDC in patients with Chronic GT1 or GT4 HCV infection and autoimmune disease
Eligible Conditions
- Chronic Hepatitis C
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ sustained virologic response 12 weeks after treatment completion
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~sustained virologic response 12 weeks after treatment completion
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
SVR12 (Sustained Virologic Response)
Trial Design
1Treatment groups
Experimental Treatment
Group I: Treatment ArmExperimental Treatment1 Intervention
12 Week treatment with LDV/SOF FDC
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
LDV/SOF FDC
2014
Completed Phase 2
~20
Find a Location
Who is running the clinical trial?
Gilead SciencesIndustry Sponsor
1,084 Previous Clinical Trials
843,439 Total Patients Enrolled
Peter J. Ruane, M.D., Inc.Lead Sponsor
2 Previous Clinical Trials
60 Total Patients Enrolled
Frequently Asked Questions
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