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NCT00043953 · ClinicalTrials.gov registry record · Phase 2

Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidovudine to Explore Metabolic Toxicities in Antiretroviral HIV-Infected Subjects

A Phase 2 study, sponsored by Abbott.

Completed
Registry status
Phase 2
Development phase
30
Enrollment target

NCT00043953 is a Phase 2 study that has completed, run by Abbott. The registered enrollment target is 30 participants.

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The verdict

NCT00043953, a Phase 2 study, has completed, sponsored by Abbott.

COMPLETED
Registry status
Phase 2
Development phase
30 participants
Enrollment target

Study Summary

The objectives of this study are to explore the metabolic toxicities associated with lopinavir/ritonavir (LPV/r) plus saquinavir mesylate (INV) versus LPV/r plus Combivir in antiretroviral naïve subjects and to assess the overall safety, tolerability and efficacy of LPV/r plus INV versus LPV/r plus Combivir in antiretroviral naïve subjects and to assess the pharmacokinetics of 400 mg INV taken twice a day (BID), 600 mg INV BID and 800 mg INV BID in combination with 400 mg lopinavir/100 mg ritonavir plus 150 mg lamivudine/300 mg zidovudine BID.

Interventions

  • DRUG Lopinavir/ritonavir
  • DRUG Saquinavir mesylate
  • DRUG Lamivudine/zidovudine

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2002-08
Phase Phase 2

Sponsor

Abbott

181 total trials

What the Registry Record Tells You About NCT00043953

The ClinicalTrials.gov registry entry for NCT00043953 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott, which has 181 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Lopinavir/ritonavir is the first listed.

NCT00043953 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00043953 about?

NCT00043953 is a clinical study titled "Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidovudine to Explore Metabolic Toxicities in Antiretroviral HIV-Infected Subjects". The objectives of this study are to explore the metabolic toxicities associated with lopinavir/ritonavir (LPV/r) plus saquinavir mesylate (INV) versus LPV/r plus Combivir in antiretroviral naïve subjects and to assess the overall safety, tolerability and efficacy of LPV/r plus INV versus LPV/r plus ...

What is the current status of trial NCT00043953?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2002-08.

What interventions are being tested in trial NCT00043953?

The interventions under investigation include: Lopinavir/ritonavir (DRUG), Saquinavir mesylate (DRUG), Lamivudine/zidovudine (DRUG).

Who is sponsoring clinical trial NCT00043953?

This trial is sponsored by Abbott, which has 181 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.