Viewing Study NCT01718301



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Last Modification Date: 2024-10-26 @ 10:58 AM
Study NCT ID: NCT01718301
Status: COMPLETED
Last Update Posted: 2015-07-09
First Post: 2012-10-25

Brief Title: HIV Patients With Chronic Hepatitis C Genotype 1 Infection Who Failed Previously to Peginterferon Ribavirin
Sponsor: Anna Cruceta
Organization: Fundacion Clinic per a la Recerca Biomédica

Study Overview

Official Title: A Study to Evaluate Safety and Efficacy of Boceprevir-response Guided Therapy in Controlled HIV Patients With Chronic Hepatitis C Genotype 1 Infection Who Failed Previously to Peginterferon Ribavirin Eudra CT2012-003984-23
Status: COMPLETED
Status Verified Date: 2015-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: BOC-HIV
Brief Summary: The primary objective of this study is to evaluate the safety and efficacy of a Response Guided Therapy of boceprevir 800 mg dosed three times a day TID orally PO in combination with Peginterferon either alpha 2b or alpha 2a and Ribavirin in HIVHCV genotype 1 infected patients that failed to previous HCV therapy
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2012-003984-23 EUDRACT_NUMBER None None