Success Metrics

Clinical Success Rate
100.0%

Based on 12 completed trials

Completion Rate
100%(12/12)
Active Trials
0(0%)
Results Posted
17%(2 trials)

Phase Distribution

Ph phase_3
8
67%
Ph phase_1
2
17%
Ph phase_2
2
17%

Phase Distribution

2

Early Stage

2

Mid Stage

8

Late Stage

Phase Distribution12 total trials
Phase 1Safety & dosage
2(16.7%)
Phase 2Efficacy & side effects
2(16.7%)
Phase 3Large-scale testing
8(66.7%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

100.0%

12 of 12 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

0

trials recruiting

Total Trials

12

all time

Status Distribution
Completed(12)

Detailed Status

Completed12

Development Timeline

Analytics

Development Status

Total Trials
12
Active
0
Success Rate
100.0%
Most Advanced
Phase 3

Trials by Phase

Phase 12 (16.7%)
Phase 22 (16.7%)
Phase 38 (66.7%)

Trials by Status

completed12100%

Recent Activity

Clinical Trials (12)

Showing 12 of 12 trials
NCT02107365Phase 2

Therapy With Asunaprevir, Daclatasvir, Ribavirin and Pegylated Interferon Alpha-2a in HCV Genotype 4-infected Patients Who Have Failed to a Previous Therapy With Peg-Interferon/Ribavirin (ANRS HC32 QUATTRO)

Completed
NCT01995266Phase 3

Phase III China GT 1b Interferon (IFN) Intolerant Prev Exclude Dual

Completed
NCT03004625Phase 3

Daclatasvir, Asunaprevir Plus Ribavirin for HCV Genotype 1b Without NS5A RAV

Completed
NCT02496078Phase 3

A Phase 3 Evaluation of Daclatasvir and Asunaprevir in Treatment-naive Subjects With Chronic Hepatitis C Genotype 1b Infection

Completed
NCT01428063Phase 2

Study of pegInterferon Alfa-2a, Ribavirin, and Daclatasvir (BMS-790052) With or Without BMS-650032 for Participants in Some Hepatitis C Virus Trials

Completed
NCT02282709Phase 3

Effect of ASV and DCV Therapy on the Quality of Immune Status in Chronic HCV Patients

Completed
NCT01973049Phase 3

UNITY 2: A Study of an Investigational Treatment Regimen of DCV+ASV+BMS-791325 in a Fixed Dose Combination (the DCV 3DAA (Direct Acting Antiviral) Regimen) With or Without RBV for 12 Weeks for the Treatment of Chronic Hepatitis C Virus(HCV)Genotype 1 Infection in Subjects With Compensated Cirrhosis

Completed
NCT01573351Phase 3

Phase III Hallmark QUAD: ASV+DCV+Peg+Rib (Nulls/Partials)

Completed
NCT01718145Phase 3

A Phase 3, Comparative Study of Asunaprevir and Daclatasvir Combination Therapy Versus Telaprevir Therapy in Japanese HCV Subjects

Completed
NCT02123654Phase 3

UNITY 3: A Japanese Phase 3 Study of a Daclatasvir/Asunaprevir/BMS-791325 in Subjects With Genotype 1 Chronic Hepatitis C

Completed
NCT02323594Phase 1

A Bioequivalence Study of Daclatasvir Tablets and Bioavailability Studies of Daclatasvir and Asunaprevir

Completed
NCT01886599Phase 1

Study of the Pharmacokinetics and Safety of Asunaprevir in Patients With Kidney Disease

Completed

All 12 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
12