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NCT00920296 · ClinicalTrials.gov registry record · Phase 1

DDI Study of Etravirine and GSK1265744

A Phase 1 study of Healthy Subjects and Infection, Human Immunodeficiency Virus, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
12
Enrollment target
1
Study location

NCT00920296: Completed Phase 1 study of Healthy Subjects and Infection, Human Immunodeficiency Virus, sponsored by GlaxoSmithKline.

NCT00920296 is a Phase 1 study of Healthy Subjects and Infection, Human Immunodeficiency Virus that has completed, run by GlaxoSmithKline. The registered enrollment target is 12 participants, below the 128-participant average among 69 other Healthy Subjects trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00920296, a Phase 1 study of Healthy Subjects and Infection, Human Immunodeficiency Virus, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
12 participants
Enrollment target
1
Study location

Study Summary

The primary objective of this study is to compare steady-state plasma PK, safety and tolerability of GSK1265744 with and without etravirine

Interventions

  • DRUG GSK1265744

Study Locations (1)

Texas

  • GSK Investigational Site - San Antonio

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2009-07
Est. Completion 2009-09
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What the finished NCT00920296 record still lists

NCT00920296 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 128-participant average among 69 other Healthy Subjects trials with a reported enrollment target (91% lower).

The record links to 2 conditions, with Healthy Subjects appearing as the primary indexed condition, and to 1 intervention - of which GSK1265744 is the first listed.

NCT00920296 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT00920296 about?

NCT00920296 is a clinical study titled "DDI Study of Etravirine and GSK1265744". The primary objective of this study is to compare steady-state plasma PK, safety and tolerability of GSK1265744 with and without etravirine

What is the current status of trial NCT00920296?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2009-07. Estimated completion is 2009-09.

What conditions does trial NCT00920296 study?

This clinical trial studies the following conditions: Healthy Subjects, Infection, Human Immunodeficiency Virus.

What interventions are being tested in trial NCT00920296?

The interventions under investigation include: GSK1265744 (DRUG).

Who is sponsoring clinical trial NCT00920296?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00920296 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy Subjects

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00920296's enrollment target sits among peer trials

12 62nd of 69 higher than 6 of 69 other Healthy Subjects trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy Subjects trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00920296, the US trial registry maintained by the National Library of Medicine. NCT00920296 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.