Hepatitis C Virus Infection Clinical Trial
Official title:
A Phase 3, Multicenter, Open-Label Study to Investigate the Efficacy and Safety of Sofosbuvir/GS-5816 Fixed Dose Combination for 12 Weeks in Subjects With Chronic HCV
The primary objectives of this study are to evaluate the efficacy, safety, and tolerability of treatment with sofosbuvir (SOF)/velpatasvir (VEL; GS-5816) fixed-dose combination (FDC) for 12 weeks in participants with chronic hepatitis C virus (HCV) infection.
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT02487030 -
Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed Dose Combination, With or Without Ribavirin, in Egyptian Adults With Chronic Genotype 4 HCV Infection
|
Phase 3 | |
| Active, not recruiting |
NCT05460130 -
Implementing HCV Treatment for High-risk Populations in Austin, Texas
|
N/A | |
| Completed |
NCT02220998 -
Comparison of Sofosbuvir/Velpatasvir Fixed Dose Combination for 12 Weeks With Sofosbuvir and Ribavirin for 12 Weeks in Adults With Chronic Genotype 2 HCV Infection
|
Phase 3 | |
| Terminated |
NCT01052090 -
Safety and Efficacy Study in Hepatitis C Patients With PHN121
|
Phase 1/Phase 2 | |
| Completed |
NCT02537379 -
Use-Results Surveillance Study of Sovaldi® Plus Copegus® in Japanese Patients With Chronic Genotype 2 Hepatitis C Virus Infection
|
N/A | |
| Recruiting |
NCT04156945 -
Interventions to Curb Hepatitis C Reinfections Among Men Who Have Sex With Men
|
N/A | |
| Terminated |
NCT02510300 -
A Registry for Adolescent and Pediatric Participants Who Received a Gilead Hepatitis C Virus Direct Acting Antiviral (DAA) in Gilead-Sponsored Chronic Hepatitis C Infection Trials
|
||
| Withdrawn |
NCT04309734 -
Study of AT-777 in Healthy Subjects and AT-777 in Combination With AT-527 in HCV-Infected Subjects
|
Phase 1/Phase 2 | |
| Active, not recruiting |
NCT04001608 -
Study of Seraprevir in Combination With Sofosbuvir in Chronic Genotype 1 Hepatitis C Virus Infection Patients
|
Phase 3 | |
| Completed |
NCT04112303 -
Study to Investigate the Efficacy and Safety of Sofosbuvir/Velpatasvir Fixed-Dose Combination for 12 Weeks in Adults With Chronic HCV Infection and Compensated Cirrhosis
|
Phase 3 | |
| Completed |
NCT02251717 -
Safety and Efficacy of Ledipasvir/Sofosbuvir (LDV/SOF) Fixed Dose Combination (FDC) for 12 or 24 Weeks in Kidney Transplant Recipients With Chronic HCV Infection
|
Phase 2 | |
| Recruiting |
NCT05092074 -
Sofosbuvir/Velpatasvir/Voxilaprevir (SOF/VEL/VOX) for Patients With Hepatitis C Virus Infection
|
||
| Recruiting |
NCT04005248 -
Prevalence of HCV in HIV-negative MSM
|
N/A | |
| Completed |
NCT02249182 -
Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed Dose Combination +/- Ribavirin in Adolescents and Children With Chronic HCV-Infection
|
Phase 2 | |
| Completed |
NCT02939989 -
Efficacy and Safety of Glecaprevir (ABT-493)/Pibrentasvir (ABT 530) (GLE/PIB) in Combination With Sofosbuvir and Ribavirin in Participants With Hepatitis C Virus Who Did Not Respond to Treatment in a Previous AbbVie Clinical Study
|
Phase 3 | |
| Completed |
NCT01718145 -
A Phase 3, Comparative Study of Asunaprevir and Daclatasvir Combination Therapy Versus Telaprevir Therapy in Japanese HCV Subjects
|
Phase 3 | |
| Completed |
NCT01482611 -
A Study in Healthy Participants Investigating the Safety, Tolerability and Plasma Pharmacokinetics (PK) of Single Oral Doses of JNJ-47910382
|
Phase 1 | |
| Completed |
NCT00255177 -
Antiviral Activity and Safety of 3 Different Doses of Mifepristone in Hepatitis C Infected Patients
|
Phase 2 | |
| Terminated |
NCT02600351 -
Efficacy and Safety of Ledipasvir/Sofosbuvir, With or Without Ribavirin, in HCV Infected Participants Who Have Failed Prior Treatment With Sofosbuvir-based Therapies
|
Phase 3 | |
| Completed |
NCT04980157 -
CARES-HCV: Promoting Screening Uptake Among Diverse Baby Boomers
|