A Study to Assess the Long-term Safety and Tolerability of TMC114/Rtv in HIV-1 Infected Participants After Rolling-over From Other TMC114 Trials

Tibotec Pharmaceutical

Status and phase

Completed

Phase 2

Conditions

HIV

Treatments

Drug: rtv

Drug: TMC114

Study type

Interventional

Funder types

Industry

Identifiers

NCT02187107

CR005848

TMC114-C208 (Other Identifier)

Details and patient eligibility

About

The purpose of this study was primarily to assess the long-term safety and tolerability of TMC114/rtv in addition to an individually optimized background antiretroviral therapy in HIV-1 infected participants. In addition, antiviral activity and immunological effect were also evaluated.

Full description

This was a phase II, open label, multicenter trial of an investigational protease inhibitor TMC114 in the presence of ritonavir (rtv) in HIV-1 infected participants who were randomized in trials TMC114-C201, TMC114-C207 or in sponsor selected phase I trials and who might derive benefit from TMC114 therapy, as judged by the investigator.

The trial consisted of a screening period of a maximum of 4 weeks, a 96-week treatment period and a 4-week follow-up period. The maximal trial duration for each participant was104 weeks. During the treatment period, all participants were receiving TMC114 in combination with RTV, orally, as 600/100 mg dose twice daily, in addition to an individually optimized background regimen of antiretroviral (ARV) therapy, selected by the investigator at a baseline of the study.

Sponsor provided a follow-up treatment with TMC114 for all participants who continued to benefit from treatment with TMC114/RTV until it became commercially available for the participant. Participants, who completed the 96 weeks of treatment period with TMC114, had the opportunity to roll over to the extension of this trial, if TMC114 was not locally commercially available.

Enrollment

52 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

Must be diagnosed with HIV
Previously randomized in trials TMC114-C201, TMC114-C207 or in sponsor selected Phase I trials
Agreed to take at least 2 antiretroviral agents from baseline onwards
Could comply with the protocol requirements
General medical condition, in the investigator's opinion, was not interfering with the assessments and the conduct of the trial

Exclusion Criteria:

A disallowed concomitant therapy
Current or past history of active alcohol and/or drug use
Pregnant or breast-feeding females
Any active or unstable medical condition (e.g., tuberculosis; cardiac dysfunction; pancreatitis; acute viral infections)
Clinical or laboratory evidence of active liver disease, liver impairment/dysfunction or cirrhosis
Clinically significant allergy or hypersensitivity to any of the excipients of the investigational medication
Laboratory abnormalities at screening (criteria variable according to the test)