Found 10 matching trials
Phase 1 Study of Relative Bioavailability of PPI-668 New Tablet Versus Capsule Formulations PHASE1 This study will compare the blood levels of PPI-668 resulting from two diff...
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Buffalo Clinical Research Center
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A Study to Evaluate the Pharmacokinetics and Safety of ASC16 Tablets in Healthy Volunteers in China PHASE1 The purpose of this study is to evaluate the pharmacokinetics and safety of...
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First Hospital of Zhejiang Province
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A Phase 1 Bioequivalence Study of a Test Tablet Formulation of Ravidasvir With the Reference Tablet Formulation of Ravidasvir Study PHASE1 In a phase 1, open-label, crossover study to evaluate the relative bioavail...
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Pharmacokinetics and Safety of Ravidasvir and Danoprevir/r in Healthy Volunteers China PHASE1 The purpose of this study is to evaluate the Pharmacokinetics and safety of...
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Multiple Locations
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Pharmacokinetics and Safety of ASC16 Tablets in Healthy Volunteers in China PHASE1 The purpose of this study is to investigate the Pharmacokinetics and Safety...
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The first hospital of Zhejiang province
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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. PHASE2 The purpose of this study is to assess the efficacy and safety of Ravidasvi...
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Peking University People's hospital
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Phase 1 Study of Relative Bioavailability of PPI-668 Tablet and Capsule Formulations PHASE1 This study will compare the blood levels of PPI-668 resulting from two diff...
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Buffalo Clinical Research Center
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8- Versus 12-week of Sofosbuvir-ravidasvir Treatment of Chronic Hepatitis C PHASE2 This is open-label, randomized, multicentre study to compare the efficacy a...
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Hospital Sultanah Bahiyah
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A Study of the Relative Bioavailability of ASC18 Tablets vs Reference Tablets in Healthy Volunteers PHASE1 The objective of this study is to evaluate potential drug interaction betwe...
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Xiangya Hospital Central South University
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Efficacy and Safety of Ravidasvir + Danoprevir/r 12-week Oral Therapy in Treatment-Naive Non Cirrhotic G1 CHC Taiwan PHASE2 The purpose of this study is to evaluate the efficacy, safety and tolerabil...
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Multiple Locations
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