ClinicalTrials.Veeva

Menu

A Follow-up Study to Assess Resistance to ABT-072 in HCV-infected Subjects Administered ABT-072 in Prior ABT-072 Studies

AbbVie logo

AbbVie

Status and phase

Completed
Phase 2

Conditions

Hepatitis C Virus Infection

Treatments

Drug: ABT-072

Study type

Interventional

Funder types

Industry

Identifiers

NCT00872196
M10-605

Details and patient eligibility

About

This is a follow-up study with no treatment and only samples being collected.

Full description

The purpose of this study is to evaluate the development of specific viral mutations in response to treatment with ABT-072.

Enrollment

5 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Main Selection Criteria: A subject that has received either ABT-072 or placebo in a prior study involving ABT-072.

Exclusion criteria

  • The investigator considers the subject unsuitable for the study for any reasons inclusive of, but not limited to, failure to comply with study procedures in a prior ABT-072 clinical study.

Trial design

5 participants in 1 patient group

1 - Follow-up Study
Other group
Description:
This is a follow-up study with no treatment and only samples being collected.
Treatment:
Drug: ABT-072

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems