Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis

NATerminatedINTERVENTIONAL
Enrollment

13

Participants

Timeline

Start Date

June 30, 2012

Primary Completion Date

July 31, 2015

Study Completion Date

August 31, 2015

Conditions
Primary Biliary Cirrhosis
Interventions
DRUG

TDF/FTC/LPV/r

one tablet of Truvada a day at standard dose of Tenofovir 300mg and Emtricitabine 200mg and four tablets of Kaletra once a day for a total dose of lopinavir 800mg and ritonavir 200mg for 6 months or less if adverse events occur

DRUG

Placebo

6 months therapy with blinded placebo followed by 6 months open label therapy with Kaletra and Truvada.

Trial Locations (1)

T6G 2B2

University of Alberta, Edmonton

Sponsors

Collaborators (2)

All Listed Sponsors
collaborator

Abbott

INDUSTRY

collaborator

Gilead Sciences

INDUSTRY

collaborator

Canadian Institutes of Health Research (CIHR)

OTHER_GOV

lead

University of Alberta

OTHER

NCT01614405 - Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Biotech Hunter | Biotech Hunter