ruzasvir: Clinical Trials

10 trials of ruzasvir, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

8 completed, 2 terminated. 5 Phase 1, 5 Phase 2.

By phase and status

PhaseTrialsStatus
Phase 15Completed 5
Phase 25Completed 3, Terminated 2

Follow ruzasvir: new trials by email Literature Review of ruzasvir trials Research Report on ruzasvir

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Drug-drug Interaction Study of Bemnifosbuvir/Ruzasvir (BEM/RZR) and Ethinyl Estradiol/Levonorgestrel (EE/LNG)
Ethinyl Estradioll/Levonorgestrel (EE/LNG), Bemnifosbuvir/Ruzasvir (BEM/RZR), Bemnifosbuvir/Ruzasvir (BEM/RZR) + Ethinyl Estradioll/Levonorgestrel (EE/LNG) - Healthy Volunteer Study
Phase 1CompletedAtea Pharmaceuticals, Inc.242025-12-042026-04-13
Pharmacokinetics of Fixed-Dose Combination Tablet of Bemnifosbuvir and Ruzasvir
Bemnifosbuvir (BEM)/Ruzasvir (RZR) FDC under fasting conditions, Bemnifosbuvir (BEM)/Ruzasvir (RZR) FDC under fed conditions, Bemnifosbuvir (BEM) and Ruzasvir (RZR) as reference formulation under fasting conditions - Healthy Volunteer Study
Phase 1CompletedAtea Pharmaceuticals, Inc.422023-12-142024-09-19
A Phase 2, Safety and Efficacy of Bemnifosbuvir (BEM) and Ruzasvir (RZR) in Subjects With Chronic HCV
Bemnifosbuvir, Ruzasvir - Chronic Hepatitis C Virus, Hepatitis C, Chronic
Phase 2CompletedAtea Pharmaceuticals, Inc.2752023-05-302025-10-21
Drug-drug Interaction Study of Ruzasvir and Bemnifosbuvir
Cohort 1 BEM + Ruzasvir, Cohort 2 Ruzasvir + BEM - Healthy Volunteer Study
Phase 1CompletedAtea Pharmaceuticals, Inc.322023-01-302023-06-01
Efficacy and Safety of Uprifosbuvir (MK-3682) + Ruzasvir (MK-8408) in Treating Hepatitis C Virus Infection Genotypes 1-6 (MK-3682-041)
Uprifosbuvir, Ruzasvir, Ribavirin - Hepatitis C
Phase 2TerminatedMerck Sharp & Dohme LLC2822016-11-162021-02-02
Efficacy and Safety of Uprifosbuvir (MK-3682) With Ruzasvir (MK-8408) in Adults With Chronic Hepatitis C Genotype 1, 2, 3, 4, 5 or 6 Infection (MK-3682-035)
Uprifosbuvir 450 mg, Ruzasvir 60 mg - Hepatitis C, Chronic
Phase 2TerminatedMerck Sharp & Dohme LLC1602016-05-032019-06-26
A Study of the Pharmacokinetics of Uprifosbuvir (MK-3682) and Ruzasvir (MK-8408) in Participants With Moderate and Severe Hepatic Insufficiency (MK-3682-029)
Uprifosbuvir, Ruzasvir - Hepatitis C, Chronic
Phase 1CompletedMerck Sharp & Dohme LLC242016-01-222018-09-17
Efficacy and Safety of Grazoprevir (MK-5172) and Uprifosbuvir (MK-3682) With Elbasvir (MK-8742) or Ruzasvir (MK-8408) for Chronic Hepatitis C Virus (HCV) Genotype (GT) 3, GT4, GT5, and GT6 Infection (MK-3682-012)
Grazoprevir, Uprifosbuvir, Elbasvir - Hepatitis C
Phase 2CompletedMerck Sharp & Dohme LLC4132015-01-282019-07-30
Efficacy and Safety of Grazoprevir (MK-5172) and Uprifosbuvir (MK-3682) With Elbasvir (MK-8742) or Ruzasvir (MK-8408) for Chronic Hepatitis C Genotype (GT)1 and GT2 Infection (MK-3682-011)
Grazoprevir, Uprifosbuvir, Elbasvir - Hepatitis C
Phase 2CompletedMerck Sharp & Dohme LLC4432015-01-222019-07-23
Safety, Pharmacokinetics, and Pharmacodynamics of Ruzasvir (MK-8408) in Participants With Hepatitis C Infection (MK-8408-003)
Ruzasvir - Hepatitis C Infection
Phase 1CompletedMerck Sharp & Dohme LLC222014-03-272018-12-24

Conditions studied

Hepatitis C (5)  ·  Hepatitis C, Chronic (3)  ·  Liver Cirrhosis (1)

Sponsors

Merck Sharp & Dohme LLC (6)  ·  Atea Pharmaceuticals, Inc. (4)

Countries

Canada (3)  ·  United States (2)  ·  Brazil (1)  ·  India (1)  ·  Mauritius (1)  ·  Moldova (1)  ·  Pakistan (1)  ·  Philippines (1)  ·  Romania (1)  ·  South Africa (1)  ·  South Korea (1)  ·  Turkey (Türkiye) (1)

Results publications

PMID 28802814, PMID 28802816, PMID 31108015, PMID 30739366

NIH funding

2014 (2), 2016 (1)