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NCT00442962 · ClinicalTrials.gov registry record · Phase 4

HIV Treatment Reinitiation in Women Who Received Anti-HIV Drugs to Prevent Mother-to-Child Transmission of HIV

A Phase 4 study, sponsored by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections.

Completed
Registry status
Phase 4
Development phase
54
Enrollment target

NCT00442962: Completed Phase 4 study, sponsored by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections.

NCT00442962 is a Phase 4 study that has completed, run by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections. The registered enrollment target is 54 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00442962, a Phase 4 study, has completed, sponsored by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections.

COMPLETED
Registry status
Phase 4
Development phase
54 participants
Enrollment target

Study Summary

The purpose of this study is to determine if pregnancy-limited, short-term combination HIV treatment regimens -- which were used solely for the prevention of mother to child transmission of HIV and discontinued postpartum -- decreases the effectiveness of a standard initial regimen of anti-HIV drugs when subsequent treatment is needed.

Primary Outcome

Plasma HIV-1 Viral Load Fewer Than 400 Copies/ml

Interventions

  • DRUG Efavirenz
  • DRUG Emtricitabine/Tenofovir disoproxil fumarate

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2007-05
Est. Completion 2010-12
Phase Phase 4

What the finished NCT00442962 record still lists

NCT00442962 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 2 interventions - of which Efavirenz is the first listed.

NCT00442962 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00442962 about?

NCT00442962 is a clinical study titled "HIV Treatment Reinitiation in Women Who Received Anti-HIV Drugs to Prevent Mother-to-Child Transmission of HIV". The purpose of this study is to determine if pregnancy-limited, short-term combination HIV treatment regimens -- which were used solely for the prevention of mother to child transmission of HIV and discontinued postpartum -- decreases the effectiveness of a standard initial regimen of anti-HIV drugs...

What is the current status of trial NCT00442962?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 54 participants. The study started on 2007-05. Estimated completion is 2010-12.

What interventions are being tested in trial NCT00442962?

The interventions under investigation include: Efavirenz (DRUG), Emtricitabine/Tenofovir disoproxil fumarate (DRUG).

Who is sponsoring clinical trial NCT00442962?

This trial is sponsored by Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections, which has 45 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00442962's enrollment target sits among peer trials

54 1223rd of 2000 higher than 772 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT00442962, the US trial registry maintained by the National Library of Medicine. NCT00442962 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.