CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 75 enrolled
Drug / intervention
Raltegravir +4 moredrug
Likely dose
Raltegravir 400mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00772590
NCT00772590Phase 4Completed

Randomised Double-blind Placebo Controlled Study to Measure the Effect of Antiretroviral Therapy (ART) Intensification With Raltegravir and/or Hyper-immune Bovine Colostrum on CD4+ T Cell Count in ART Treated, HIV-1 Infected Individuals With Suboptimal CD4+ T Cell Responses

Kirby Institute·interventional·Posted Oct 15, 2008·Updated Aug 24, 2012

In Brief

A Phase 4 clinical trial evaluating Raltegravir, Hyper-immune Bovine Colostrum, and 3 other interventions for HIV Infections. Completed, enrolled 75 participants.

Detailed Summary

A research study to measure the effect on CD4 counts of adding to current anti-retroviral regimen raltegravir with or without hyper-immune bovine colostrum.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHIV Infections
Countries--
Collaborators--

Timeline

Phase 4CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 15, 2008
Enrollment StartMar 1, 2009
Primary CompletionMar 1, 2010
Study CompletionJun 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 17.7 years ago

Interventions

Raltegravirdrug

Tablets, 400mg, twice daily

Hyper-immune Bovine Colostrumdrug

Tablet, 1800mg, twice daily

raltegravir placeboother

One tablet, twice daily

Hyper-immune Bovine Colostrum placeboother

Three tablets twice daily

raltegravir and hyper-immune bovine colostrumdrug

400mg twice daily raltegravir and 1800mg twice daily of hyper-immune bovine colostrum