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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 weeks
Treatment ~ Varies
Follow Up ~sustained virologic response 12 weeks after treatment completion
This trial's timeline: 3 weeks for screening, Varies for treatment, and sustained virologic response 12 weeks after treatment completion for reporting.

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

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~4 spots leftby Apr 2025