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OpenTrials
Completed

NCT Number: NCT00781976

Antiviral Activity of AZD7295 in HCV Carriers

PK, safety study of AZD7295 in HCV carriers

Completed

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Key information

Conditions

Hepatitis C Blood-Borne Infections Communicable Diseases Digestive System Diseases Flaviviridae Infections Hepatitis Hepatitis, Viral, Human Infections Liver Diseases RNA Virus Infections Virus Diseases

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Prof Ed Gane

Auckland, New Zealand

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HCV carrier

Exclusion criteria

  • concurrent medications

Treatment and study plan

AZD7295

Drug

700mg per day maximum

Placebo

Drug

matched placebo

Primary outcomes

  1. Plasma AZD7295 concentrations and pharmacokinetics

    Time frame: 5 days

Interested in participating?

Completed

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Sponsors and collaborators

Lead sponsor

Arrow Therapeutics

Industry

Registry information

Official study title

A Randomised, DB, PC Study to Determine the PK, Safety and Tolerability Profile and Antiviral Activity of Multiple Oral Doses of AZD7295 in Otherwise Healthy Male and Female Hepatitis C Carriers With Compensated Liver Disease

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Oct 29, 2008
Registry last updated
Mar 31, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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