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Phase 2 Completed N=33 Randomized Treatment

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

Human Immunodeficiency Virus Type 1
Source: ClinicalTrials.gov NCT00838162 ↗
Enrolled (actual)
33
Serious AEs
0.0%
Results posted
Mar 2013
Primary outcomePrimary: Mean Changes From Baseline in Plasma log10 Human Immunodeficiency Virus Type 1 Ribonucleic Acid (HIV-1 RNA) — 4.72; 4.36; 4.78; 4.71 log10 copies/mL

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Mean Changes From Baseline in Plasma log10 Human Immunodeficiency Virus Type 1 Ribonucleic Acid (HIV-1 RNA)
4.72; 4.36; 4.78; 4.71; -1.30; -1.14
SECONDARY
Number of Participants With Virologic Response at Any Timepoint During the 14-day Treatment Period
0; 1; 0; 0; 3; 4
SECONDARY
Mean Changes From Baseline in CD4+ Cell Count
575.7; 464.9; 494.0; 479.6; -21.0; 40.3
SECONDARY
Maximum Plasma Concentration (Cmax) of TMC310911
487.9; 623.0; 706.3; 1924; 589.7; 1674
SECONDARY
Time to Reach the Maximum Plasma Concentration (Tmax) of TMC310911
5.02; 5.00; 5.06; 5.00; 4.98; 3.00
SECONDARY
Area Under the Plasma Concentration-time Curve (AUC12) From the Time of Administration of TMC310911 up to 12 Hours After Dosing
2519; 2735; 2990; 10040; 4031; 10680
SECONDARY
Predose Plasma Concentration (C0h) of TMC310911
79.95; 207.7; 231.9; 45.48; 93.98; 448.0
SECONDARY
Average Steady-state Plasma Concentration (Css,av) of TMC310911
336.2; 889.6; 1340; 887.3
SECONDARY
Fluctuation Index of TMC310911
181.0; 161.3; 129.2; 331.8

Eligibility 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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00838162). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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