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NCT00002320 · ClinicalTrials.gov registry record · Phase 3

A Comparison of Lamivudine and Zidovudine, Used Alone and Together, in HIV-Infected Patients Who Have Not Used Zidovudine in the Past

A Phase 3 study, sponsored by Glaxo Wellcome.

Completed
Registry status
Phase 3
Development phase
320
Enrollment target

NCT00002320: Completed Phase 3 study, sponsored by Glaxo Wellcome.

NCT00002320 is a Phase 3 study that has completed, run by Glaxo Wellcome. The registered enrollment target is 320 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (59% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00002320, a Phase 3 study, has completed, sponsored by Glaxo Wellcome.

COMPLETED
Registry status
Phase 3
Development phase
320 participants
Enrollment target

Study Summary

To evaluate the safety and efficacy of high-dose lamivudine (3TC) alone versus zidovudine (AZT) alone versus 3TC at high and low doses in combination with AZT in HIV-1 infected patients. PER 02/27/95 AMENDMENT: To evaluate the efficacy and safety of both blinded and open-label combination therapy.

Interventions

  • DRUG Zidovudine
  • DRUG Lamivudine

Trial Details

FieldValue
Enrollment Target 320 participants
Phase Phase 3
Glaxo Wellcome

65 total trials

What the finished NCT00002320 record still lists

NCT00002320 is an interventional study that assigns participants to a tested intervention. The registered 320 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (59% lower).

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

NCT00002320 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00002320 about?

NCT00002320 is a clinical study titled "A Comparison of Lamivudine and Zidovudine, Used Alone and Together, in HIV-Infected Patients Who Have Not Used Zidovudine in the Past". To evaluate the safety and efficacy of high-dose lamivudine (3TC) alone versus zidovudine (AZT) alone versus 3TC at high and low doses in combination with AZT in HIV-1 infected patients. PER 02/27/95 AMENDMENT: To evaluate the efficacy and safety of both blinded and open-label combination therapy.

What is the current status of trial NCT00002320?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 320 participants.

What interventions are being tested in trial NCT00002320?

The interventions under investigation include: Zidovudine (DRUG), Lamivudine (DRUG).

Who is sponsoring clinical trial NCT00002320?

This trial is sponsored by Glaxo Wellcome, which has 65 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00002320's enrollment target sits among peer trials

320 1082nd of 2000 higher than 914 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT00002320, the US trial registry maintained by the National Library of Medicine. NCT00002320 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.