Success Metrics

Clinical Success Rate
100.0%

Based on 28 completed trials

Completion Rate
100%(28/28)
Active Trials
0(0%)
Results Posted
11%(3 trials)

Phase Distribution

Ph phase_3
1
3%
Ph phase_2
8
28%
Ph phase_1
20
69%

Phase Distribution

20

Early Stage

8

Mid Stage

1

Late Stage

Phase Distribution29 total trials
Phase 1Safety & dosage
20(69.0%)
Phase 2Efficacy & side effects
8(27.6%)
Phase 3Large-scale testing
1(3.4%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

96.6%

28 of 29 finished

Non-Completion Rate

3.4%

1 ended early

Currently Active

0

trials recruiting

Total Trials

29

all time

Status Distribution
Completed(28)
Terminated(1)

Detailed Status

Completed28
Withdrawn1

Development Timeline

Analytics

Development Status

Total Trials
29
Active
0
Success Rate
100.0%
Most Advanced
Phase 3

Trials by Phase

Phase 120 (69.0%)
Phase 28 (27.6%)
Phase 31 (3.4%)

Trials by Status

completed2897%
withdrawn13%

Recent Activity

Clinical Trials (29)

Showing 20 of 29 trialsScroll for more
NCT03020082Phase 3

Efficacy and Safety of Danoprevir/r + PR 12week Triple Therapy in Treatment Naive Non-Cirrhotic G1 CHC China III

Completed
NCT03020095Phase 2

Efficacy and Safety of Ravidasvir + Danoprevir/r 12-week Oral Therapy in Treatment-Naive Non Cirrhotic G1 CHC Taiwan

Completed
NCT03362814Phase 2

Efficacy and Safety of Ravidasvir in Combination With Danoprevir/r and Ribavirin(RBV) in Treatment-naive, Non-cirrhotic, Chronic Hepatitis C Virus Genotype1 Infected Subjects.

Completed
NCT03020004Phase 2

Efficacy and Safety of Danoprevir/r + PR 12-week Triple Therapy in Treatment-Naive, Non-Cirrhotic, G1 CHC China II

Completed
NCT03020134Phase 1

Pharmacokinetics and Safety of Ravidasvir and Danoprevir/r in Healthy Volunteers China

Completed
NCT03288636Phase 1

Pharmacokinetics and Safety of ASC16 Tablets in Healthy Volunteers in China

Completed
NCT03019991Phase 1

Safety, Tolerability and Pharmacokinetics of Danoprevir/r in Healthy Volunteers China

Completed
NCT01531647Phase 1

A Study of Drug-Drug Interaction Between Danoprevir/Low-Dose Ritonavir and Raltegravir in Healthy Volunteers

Completed
NCT01592318Phase 1

A Study of The Relative Bioavailability of Ritonavir-Boosted Danoprevir Fixed Dose Combination Tablets in Healthy Volunteers

Completed
NCT01389544Phase 1

A Study on the Interaction Between Danoprevir/Ritonavir and Methadone

Completed
NCT01714154Phase 1

A Safety And Pharmacokinetic Study of Setrobuvir Alone and In Combination With Ritonavir-Boosted Danoprevir in Subjects With Mild Hepatic Impairment Compared to Healthy Controls

Completed
NCT01398293Phase 1

A Study of Danoprevir in Combination With Low-Dose Ritonavir in Healthy Subjects

Completed
NCT00801255Phase 1

A Study of Combination Treatment With an HCV Polymerase Inhibitor (RO5024048) and an HCV Protease Inhibitor (RO5190591/Danoprevir) in Genotype 1 Chronic Hepatitis C Patients

Completed
NCT01331850Phase 2

A Study of Danoprevir/Ritonavir and Copegus With RO5024048 and/or Pegasys in Patients With Chronic Hepatitis C

Completed
NCT01514968Phase 1

A Drug-Drug Interaction Study Between Danoprevir/Low-Dose Ritonavir and Cyclosporine in Healthy Volunteers

Completed
NCT01592305Phase 1

A Study of Drug-Drug Interaction Between Danoprevir Coadministered With Low-Dose Ritonavir and Tenofovir Disoproxil Fumarate or Atazanavir

Completed
NCT01654211Phase 1

A Pharmacokinetic And Bioavailability Study of Intravenous Danoprevir in Healthy Volunteers

Completed
NCT01220947Phase 2

A Study of Danoprevir Boosted With Low Dose Ritonavir in Combination With Pegasys and Copegus in Treatment-Naive Patients With Chronic Hepatitis C Virus Infection

Completed
NCT01185873Phase 1

A Study of Danoprevir in Healthy Volunteers And Patients With Hepatic Impairment

Completed
NCT01519336Phase 1

A Study of Drug-Drug Interaction Between Darunavir and Danoprevir Administered Together With Low-Dose Ritonavir in Healthy Volunteers

Completed

Drug Details

Intervention Type
DRUG
Total Trials
29