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Paritaprevir

Alternative Names: paritaprevir, abt-450, viekira xr, technivie, viekira pak (copackaged), viekira pak
Latest Update: 2024-08-23
Latest Update Note: Clinical Trial Update

Product Description

Paritaprevir is a direct acting antiviral medication used as part of combination therapy to treat chronic Hepatitis C, an infectious liver disease caused by infection with Hepatitis C Virus (HCV). (Sourced from: https://pubchem.ncbi.nlm.nih.gov/compound/Paritaprevir)

Mechanisms of Action: HCV-NS3/4A Inhibitor,SP

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: Austria | Belgium | Canada | Chile | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hungary | Iceland | Ireland | Italy | Japan | Korea | Latvia | Lithuania | Netherlands | New Zealand | Norway | Peru | Poland | Portugal | Romania | Russia | Serbia | Slovakia | Slovenia | Spain | Sweden | Taiwan | Tunisia | Turkey | Ukraine | United Kingdom | United States | Venezuela

Approved Indications: Liver Cirrhosis | Hepatitis | Hepatitis, Chronic | Hepatitis C | Hepatitis C, Chronic | Liver Cirrhosis | Hepatitis | Hepatitis, Chronic | Hepatitis C | Hepatitis C, Chronic

Known Adverse Events: Insomnia | Pruritus | Asthenia | Headache Disorders | Dizziness | Headache | Pain Unspecified | Liver Cirrhosis | Musculoskeletal Pain | Dyspnea

Company: AbbVie
Company Location: NORTH CHICAGO IL 60064
Company CEO: Richard A. Gonzalez
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Paritaprevir

Countries in Clinic:

Active Clinical Trial Count: 1

Highest Development Phases

Phase 3: Hepatitis C, Chronic

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2015-000111-41

P3

Completed

Hepatitis C, Chronic

2023-05-01

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