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NCT00401947

A Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of ACH-0137171 in Participants With Chronic Hepatitis C Infection

Terminated Phase 2 Last updated 15 September 2022
What this trial tests

Phase 2 trial testing ACH-0137171 in HCV Infection in 30 participants. Terminated before completion.

Timeline
30 November 2006
31 March 2007

Quick facts

Lead sponsorAlexion Pharmaceuticals, Inc.
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingdouble
Primary purposetreatment
Enrollment30
Start date30 November 2006
Estimated completion31 March 2007
Sites9 locations across Netherlands, United States, Germany

Drugs / interventions tested

Conditions studied

Sponsor

Alexion Pharmaceuticals, Inc. — full company profile →

Who can join

Adults 18 to 60, any sex, with HCV Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study was to investigate the safety, tolerability, pharmacokinetics (PK), and antiviral activity of multiple doses of ACH-0137171 in participants with chronic hepatitis C virus (HCV) infection.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for HCV Infection

Currently open trials in the same condition.

Other Alexion Pharmaceuticals, Inc. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00401947.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing