Key Insights

Highlights

Success Rate

93% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

5.6%

1 terminated out of 18 trials

Success Rate

92.9%

+6.4% vs benchmark

Late-Stage Pipeline

11%

2 trials in Phase 3/4

Results Transparency

15%

2 of 13 completed with results

Key Signals

2 with results93% success

Data Visualizations

Phase Distribution

14Total
P 1 (6)
P 2 (6)
P 3 (2)

Trial Status

Completed13
Withdrawn2
Unknown2
Terminated1

Trial Success Rate

92.9%

Benchmark: 86.5%

Based on 13 completed trials

Clinical Trials (18)

Showing 18 of 18 trials
NCT04382937Phase 3CompletedPrimary

Ropeginterferon Alfa-2b (P1101) Phase 3 Study in Interferon Treatment-Naive Subjects With HCV Genotype 2 Infection

NCT02292719Phase 2CompletedPrimary

A Study to Evaluate the Safety and Efficacy of Ombitasvir/ABT-450/Ritonavir With Sofosbuvir With or Without Ribavirin in Adults With Chronic Hepatitis C Virus Infection

NCT01080222Phase 2TerminatedPrimary

A Safety and Efficacy Study of the Combination of VX-222 and Telaprevir in Treatment-Naïve Subjects With Genotype 1 Chronic Hepatitis C Virus Infection

NCT04391985Phase 1CompletedPrimary

Sofosbuvir/Ombitasvir/Paritaprevir/ Ritonavir and Ribavirin for Hepatitis C Virus Genotype 4 Patients

NCT04387526Phase 2CompletedPrimary

Sofosbuvir Plus Daclatasvir With or Without Ribavirin and Chronic HCV Genotype (GT) 4

NCT04387539Phase 1CompletedPrimary

ٍٍSofosbuvir/Simeprevir/Daclatasvir/Ribavirin and HCV Genotype 4-infected Egyptian Experienced Participants

NCT04385407Phase 2CompletedPrimary

Sofosbuvir With Ribavirin or Simeprevir With HCV GT4 Egyptian Patients

NCT00851890Phase 2CompletedPrimary

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Multiple Doses of ABT-333 Alone and in Combination With Pegylated Interferon (pegIFN) and Ribavirin (RBV) in Subjects With Genotype 1 Chronic Hepatitis C Virus (HCV) Infection

NCT01813266WithdrawnPrimary

Prospective Cohort Study: To Provide Evidence & Guidance in Hepatitis C Virus Screening, Comparing the New Birth Cohort Recommendations From the CDC, Versus Classical Traditional Strategies With Established Risk Factors

NCT00606528CompletedPrimary

FGL2/Fibroleukin and Hepatitis C Virus Infection: A Predictor of Response to Antiviral Therapy

NCT01708889Phase 1Completed

Pharmacokinetic Study of BMS-914143 in Participants With Normal Renal Function and Mild, Moderate, Severe and End-stage Renal Dysfunction

NCT01121731Phase 1CompletedPrimary

A Phase I/II Clinical Trial With Interferon Alfa 5 in Treatment-Experienced Patients With Genotype-1 Chronic Hepatitis C

NCT00570336Phase 2CompletedPrimary

Study of CTS-1027 in Hepatitis C Patients

NCT00563173Phase 1UnknownPrimary

Phase I/IIa Dose Ranging CHRONVAC-C® Study in Chronic HCV Patients

NCT00770198Completed

sgp130 in Chronic Human Liver Disease

NCT00255359Phase 1WithdrawnPrimary

Safety, Tolerability and Efficacy of XTL 2125 in HCV-Infected Patients Who Are Interferon-Alpha Non-Responders or Relapsers

NCT00294489UnknownPrimary

Methacetin Breath Test in HCV Patients With Normal and Near-Normal ALT

NCT00215865Phase 3CompletedPrimary

PEG-Interferon a-2b + Ribavirin for Treatment of Patients With Chronic Hepatitis C Who Have Previously Failed to Achieve a Sustained Virologic Response Following Interferon Alfa or Interferon a-2b + Ribavirin Therapy

Showing all 18 trials

Research Network

Activity Timeline