Success Metrics

Clinical Success Rate
100.0%

Based on 28 completed trials

Completion Rate
100%(28/28)
Active Trials
0(0%)
Results Posted
82%(23 trials)

Phase Distribution

Ph phase_3
13
46%
Ph phase_1
1
4%
Ph phase_2
11
39%

Phase Distribution

1

Early Stage

11

Mid Stage

13

Late Stage

Phase Distribution25 total trials
Phase 1Safety & dosage
1(4.0%)
Phase 2Efficacy & side effects
11(44.0%)
Phase 3Large-scale testing
13(52.0%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

100.0%

28 of 28 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

0

trials recruiting

Total Trials

28

all time

Status Distribution
Completed(28)

Detailed Status

Completed28

Development Timeline

Analytics

Development Status

Total Trials
28
Active
0
Success Rate
100.0%
Most Advanced
Phase 3

Trials by Phase

Phase 11 (4.0%)
Phase 211 (44.0%)
Phase 313 (52.0%)

Trials by Status

completed28100%

Recent Activity

Clinical Trials (28)

Showing 20 of 28 trialsScroll for more
NCT03487107Phase 3

Phase 3 Study of Yimitasvir Phosphate Capsules

Completed
NCT03458481Phase 2

Phase 2 Study of Yimitasvir Phosphate Capsules

Completed
NCT02175758Phase 2

Safety and Efficacy of Sofosbuvir + Ribavirin in Adolescents and Children With Genotype 2 or 3 Chronic HCV Infection

Completed
NCT01826981Phase 2

Efficacy and Safety of Sofosbuvir Containing Regimens for the Treatment of Chronic HCV Infection in Participants With Chronic Genotype 1, 2, 3, or 6 HCV Infection

Completed
NCT02201953Phase 3

Comparison of Sofosbuvir/Velpatasvir Fixed Dose Combination for 12 Weeks With Sofosbuvir and Ribavirin for 24 Weeks in Adults With Chronic Genotype 3 HCV Infection

Completed
NCT02738333Phase 3

Ledipasvir/Sofosbuvir Fixed-Dose Combination for 12 Weeks in Participants With Chronic Genotype 2 HCV Infection

Completed
NCT02220998Phase 3

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

Completed
NCT01909804Phase 2

Safety and Efficacy of Sofosbuvir Plus Velpatasvir With or Without Ribavirin in Treatment-experienced Subjects With Chronic HCV Infection

Completed
NCT01858766Phase 2

Safety and Efficacy of Sofosbuvir + Velpatasvir With or Without Ribavirin in Treatment-Naive Adults With Chronic HCV Infection

Completed
NCT01958281Phase 2

Sofosbuvir Plus Ribavirin, or Ledipasvir/Sofosbuvir in Adults With HCV Infection and Renal Insufficiency

Completed
NCT02592057

Safety and Efficacy of Sofosbuvir-based Regimens in Clinical Practice for the Treatment of Chronic Hepatitis C Virus Infection in India

Completed
NCT02673489Phase 3

A Study of Daclatasvir and Sofosbuvir With Ribavirin in Subjects With Cirrhosis and Genotype 3 Hepatitis C Infection

Completed
NCT02562742

Use-Results Surveillance Study of Sovaldi® Plus Rebetol® in Japanese Patients With Chronic Genotype 2 Hepatitis C Virus Infection

Completed
NCT02537379

Use-Results Surveillance Study of Sovaldi® Plus Copegus® in Japanese Patients With Chronic Genotype 2 Hepatitis C Virus Infection

Completed
NCT01962441Phase 3

SOF (Sovaldi®) +RBV for 16 or 24 Weeks and SOF+RBV+Peg-IFN for 12 Weeks in Adults With Genotype 2 or 3 Chronic HCV Infection

Completed
NCT02120300Phase 2

Efficacy and Safety of Ledipasvir/Sofosbuvir Fixed-Dose Combination and Sofosbuvir + Ribavirin for Subjects With Chronic Hepatitis C Virus (HCV) and Inherited Bleeding Disorders

Completed
NCT01687257Phase 2

Sofosbuvir and Ribavirin in Patients With Chronic HCV With Cirrhosis and Portal Hypertension With or Without Liver Decompensation

Completed
NCT01625338Phase 3

Open-Label Study of Sofusbuvir+Ribavirin With or Without Peginterferon Alfa-2a in Subjects With Chronic HCV Infection Who Participated in Prior Gilead HCV Studies

Completed
NCT01896193Phase 3

Safety and Efficacy Study of Sofosbuvir Plus Ribavirin in Treatment-Naive Adults With Genotype 1 and 3 Chronic HCV Infection

Completed
NCT01838590Phase 3

Sofosbuvir Plus Ribavirin Administered for Either 12 or 24 Weeks in Treatment-Naive and Treatment-Experienced Egyptian Adults With Chronic Genotype 4 Hepatitis C Virus (HCV) Infection

Completed

Drug Details

Intervention Type
DRUG
Total Trials
28