Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

0.0%

0 terminated out of 20 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

45%

9 trials in Phase 3/4

Results Transparency

56%

9 of 16 completed with results

Key Signals

9 with results100% success

Data Visualizations

Phase Distribution

16Total
Not Applicable (1)
P 1 (1)
P 2 (5)
P 3 (7)
P 4 (2)

Trial Status

Completed16
Unknown2
Withdrawn2

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 16 completed trials

Clinical Trials (20)

Showing 20 of 20 trials
NCT05904470Phase 2CompletedPrimary

A Phase 2, Safety and Efficacy of Bemnifosbuvir (BEM) and Ruzasvir (RZR) in Subjects With Chronic HCV

NCT02723084Phase 3CompletedPrimary

A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adults With Genotype 2 Chronic Hepatitis C Virus Infection

NCT02707952Phase 3CompletedPrimary

A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adults With Chronic Hepatitis C Virus Infection

NCT01740791Phase 1CompletedPrimary

Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Velpatasvir in Participants With Chronic HCV Infection

NCT02945228CompletedPrimary

Drug Use-Results Survey in Participants Infected With Hepatitis C Virus Genotype 2

NCT02629172CompletedPrimary

Drug Use-results Survey in Patients Infected With Hepatitis C Virus Genotype 1

NCT01851330Phase 3CompletedPrimary

Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination ± Ribavirin for the Treatment of HCV (ION-3)

NCT01768286Phase 3CompletedPrimary

Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination ± Ribavirin in Treatment-Experienced Subjects With Genotype 1 HCV Infection

NCT01701401Phase 3CompletedPrimary

Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination (FDC) With and Without Ribavirin for the Treatment of HCV

NCT01726517Phase 2CompletedPrimary

Safety and Efficacy of LDV/SOF Fixed-Dose Combination (FDC) ± Ribavirin in HCV Genotype 1 Subjects

NCT02105467Phase 3CompletedPrimary

Study of Efficacy and Safety of Grazoprevir (MK-5172)/Elbasvir (MK-8742) Combination Regimen for Treatment-Naïve Participants With Chronic Hepatitis C Virus Genotypes 1, 4, and 6 (MK-5172-060)

NCT02806362Phase 3WithdrawnPrimary

Study of Ombitasvir/Paritaprevir/Ritonavir in Japanese Adults With Genotype 1b Chronic Hepatitis C Virus (HCV) Infection With End Stage Renal Disease (ESRD) on Hemodialysis (HD)

NCT02950870Phase 4UnknownPrimary

Efficacy Study to Evaluate the Effect of New Antiviral Drugs on HCV Infection.

NCT01686789Phase 4CompletedPrimary

Randomized Controlled Open Label Trial of Peg Alpha 2a Interferon and Adjusted-dose of Ribavirin vs. Standard Therapy in the Treatment of Naive Chronic Hepatitis C Patients Infected With Genotype 4

NCT01852604Phase 2CompletedPrimary

Samatasvir (IDX719) in Combinations With Simeprevir and/or TMC647055/Ritonavir With or Without Ribavirin for 12 Weeks in Participants With Chronic Hepatitis C Infection (MK-1894-005)

NCT01516918Phase 2CompletedPrimary

A Study to Evaluate the Efficacy and Safety of Quadruple Therapy (VX-222, Telaprevir,Peginterferon-Alfa-2a, Ribavirin) in Subjects With Chronic Hepatitis C With Compensated Cirrhosis

NCT01691235WithdrawnPrimary

SIMpill Medication Dispensing Device in the Treatment of HCV

NCT01581138Phase 2CompletedPrimary

VX-222 + Telaprevir + Ribavirin for 12 or 16 Weeks in Treatment-Naive Subjects With Genotype 1a Hepatitis C

NCT02038387Not ApplicableUnknownPrimary

Prospective Clinical Study of the Role of the Immune Response, in Relation to Diet, in Patients Affected by Either Chronic Hepatitis C Virus (HCV) Infection or Non Alcoholic Fatty Liver Disease (NAFLD)

NCT00610597Completed

Study of T Cell Phenotype Activation Pathway in Human Alcoholic Liver Disease

Showing all 20 trials

Research Network

Activity Timeline