Overview

A Study to Determine the Antiviral Activity of TMC310911 When Administered With Ritonavir in Treatment-Naive Human Immunodeficiency Virus - Type 1 (HIV-1) Infected Patients

Status:
Completed
Trial end date:
2011-02-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to evaluate the antiviral activity as measured by the change in viral load from baseline in the 14 days following initiation of treatment with 4 different dose regimens of TMC310911 co-administered with ritonavir.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tibotec Pharmaceuticals, Ireland
Treatments:
Antiviral Agents
Ritonavir
TMC-310911
Criteria
Inclusion Criteria:

- Documented human immunodeficiency virus type 1 (HIV-1) infection for at least 6 months
prior to the screening date

- Participant who has not been treated with a therapeutic HIV vaccine within 1 year
prior to enrolment and has never been treated with an antiretroviral (ARV) medication
indicated for the treatment of HIV infection or ARVs for treatment of hepatitis
B-infection with anti-HIV activity

- Participant agrees not to start antiretroviral therapy (ART) before the baseline visit

- Able to comply with the protocol requirements and have good accessible veins

- HIV-1 plasma viral load at screening visit of above 5,000 HIV-1 Ribonucleic acid
copies/mL

- CD4+ cell count above 200 cells/mm3 at screening

Exclusion Criteria:

- HIV-2 infected participants and/or participants with any active or chronic
hepato-renal disease

- Life expectancy of less than 6 months

- Documented acute (primary) HIV-1 infection

- Pre-existing protease inhibitor (PI) medication resistance

- Any currently active Acquired Immunodeficiency Syndrome (AIDS) - defining illness

- Any active clinically significant disease or findings during screening or medical
history or physical examination that in the investigator's opinion, would compromise
the outcome of the study

- Any confirmed grade 3 or 4 toxicity according to the Division of AIDS (DAIDS) grading
scale at screening