TMC114-C214: Trial of TMC114 Administered With Low Dose Ritonavir (RTV) in HIV-1 Infected Treatment Experienced Patients

Study TMC114-C214 is a randomized (patients are assigned to different treatment groups based
on chance), controlled, open-label trial to compare the efficacy (effectiveness), safety and
tolerability of TMC114 boosted with low dose ritonavir (RTV) versus Kaletra (LPV)/RTV in
treatment-experienced HIV-1 infected patients. This research study will look at the safety
of TMC114 and effectiveness in reducing the amount of HIV(viral load) in the blood. People
included in this study will have received either Non-Nucleoside Reverse Transcriptase
Inhibitors (NNRTIs) or Protease Inhibitors (PIs) or both. The duration of the study will be
approximately 106 weeks, which includes a 4 to 6 week screening period, 96-week treatment
period, and 4-week follow-up period. TMC114 300mg are orange tablets where 2 tablets are
taken by mouth twice a day with 1 tablet of Ritonavir. Kaletra (LPV/RTV) is either a tablet
or capsule taken twice a day. The oral capsule contains 133.3 mg LPV, 33.3 mg RTV and the
film-coated tablet is available for oral administration in a strength of 200 mg of lopinavir
and 50 mg of ritonavir. Dosing for all medication will occur for 96 weeks and you will be
randomly assigned to either TMC114 or Kaletra.

Inclusion Criteria:

- Patient has documented HIV-1 infection

- Treatment with an Antiretroviral regimen (containing at least 2 NRTIs in combination
with at least 1 NNRTI and/or 1 PI) for at least 12 weeks

- Plasma HIV-1 RNA >1000 copies/mL

- General medical condition does not interfere with the assessments and the completion
of the trial

Exclusion Criteria:

- Patients for whom an investigational Antiretroviral is part of the current regimen,
with the following exceptions if applicable (depending on local regulatory approval)

- tenofovir, emtricitabine, atazanavir, fosamprenavir

- Previous or current use of lopinavir, enfuvirtide (T-20), tipranavir and TMC114

- Life expectancy of less than 6 months

- Pregnant or breast-feeding

- Females of childbearing potential not willing to use effective non-hormonal birth
control methods or not willing to continue practicing these birth control methods for
at least 14 days after the end of the treatment period

- Patients with significantly decreased liver function or decompensation, irrespective
of liver enzyme levels

- Participation in other investigational trials without prior approval of the sponsor