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NCT00046176

A HIV Study Of A Fixed-Dose Combination Tablet In Antiretroviral Experienced Patients

Completed Phase 3 Last updated 24 March 2020
What this trial tests

Phase 3 trial testing abacavir/lamivudine in Infection, Human Immunodeficiency Virus I in 240 participants. Completed in 17 May 2004.

Timeline
26 August 2002
Primary endpoint
17 May 2004
17 May 2004

Quick facts

Lead sponsorViiV Healthcare
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment240
Start date26 August 2002
Primary completion17 May 2004
Estimated completion17 May 2004
Sites56 locations across Panama, Costa Rica, United States, Puerto Rico

Drugs / interventions tested

Conditions studied

Sponsor

ViiV Healthcare — full company profile →

Who can join

18 and older, any sex, with Infection, Human Immunodeficiency Virus I or HIV Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a 48-week study designed to evaluate the safety and efficacy of a fixed-dose combination tablet administered once-a-day versus the individual tablets administered twice-a-day within 3-drug combination regimens in ART (antiretroviral)-experienced HIV-1 infected patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of abacavir/lamivudine

Trials testing the same drug.

Other ViiV Healthcare trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00046176.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing