Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00455494 · ClinicalTrials.gov registry record · Phase 1

Food-Effect Bioavailability Study of AQ-13, a Candidate Antimalarial

A Phase 1 study of Malaria, sponsored by Tulane University Health Sciences Center.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target
1
Study location

NCT00455494: Completed Phase 1 study of Malaria, sponsored by Tulane University Health Sciences Center.

NCT00455494 is a Phase 1 study of Malaria that has completed, run by Tulane University Health Sciences Center. The registered enrollment target is 14 participants, below the 258-participant average among 27 other Malaria trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00455494, a Phase 1 study of Malaria, has completed, sponsored by Tulane University Health Sciences Center.

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

Study Summary

The purpose of this study is to test the safety of a 2100 mg dose of AQ-13, a new candidate antimalarial active against drug-resistant P. falciparum infection, and to determine the effect of a standard fatty meal on the absorption of the drug from the gut and its blood levels.

Conditions Studied

Interventions

  • DRUG AQ-13

Study Locations (1)

Louisiana

  • Tulane-LSU General Clinical Research Center - New Orleans

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2005-01
Est. Completion 2006-12
Phase Phase 1

What the finished NCT00455494 record still lists

NCT00455494 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 258-participant average among 27 other Malaria trials with a reported enrollment target (95% lower).

The record links to 1 condition, with Malaria appearing as the primary indexed condition, and to 1 intervention - of which AQ-13 is the first listed.

NCT00455494 reports a single indexed study location in Louisiana.

Frequently Asked Questions

What is clinical trial NCT00455494 about?

NCT00455494 is a clinical study titled "Food-Effect Bioavailability Study of AQ-13, a Candidate Antimalarial". The purpose of this study is to test the safety of a 2100 mg dose of AQ-13, a new candidate antimalarial active against drug-resistant P. falciparum infection, and to determine the effect of a standard fatty meal on the absorption of the drug from the gut and its blood levels.

What is the current status of trial NCT00455494?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2005-01. Estimated completion is 2006-12.

What conditions does trial NCT00455494 study?

This clinical trial studies the following conditions: Malaria.

What interventions are being tested in trial NCT00455494?

The interventions under investigation include: AQ-13 (DRUG).

Who is sponsoring clinical trial NCT00455494?

This trial is sponsored by Tulane University Health Sciences Center, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00455494 being conducted?

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

Similar trials for Malaria

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 NCT00455494's enrollment target sits among peer trials

14 27th of 27 higher than 1 of 27 other Malaria trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Malaria 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02523092 · 14 participants · Phase 4

    Use of CXCL9 as a Biomarker of Acthar Efficacy

  • NCT04263285 · 14 participants · NA

    Treatment of Depression Post-SCI

  • NCT04743271 · 14 participants · NA

    Food and Circadian Timing

  • NCT05065671 · 14 participants · Phase 1

    Microbiome Derived Metabolism and Pharmacokinetics

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00455494, the US trial registry maintained by the National Library of Medicine. NCT00455494 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.