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NCT00984256 · ClinicalTrials.gov registry record · Phase 2

Weekly Dosing of Malarone ® for Prevention of Malaria

A Phase 2 study of Malaria, sponsored by U.S. Army Medical Research and Development Command.

Completed
Registry status
Phase 2
Development phase
35
Enrollment target
1
Study location

NCT00984256 is a Phase 2 study of Malaria that has completed, run by U.S. Army Medical Research and Development Command. The registered enrollment target is 35 participants, below the 257-participant average among 27 other Malaria trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00984256, a Phase 2 study of Malaria, has completed, sponsored by U.S. Army Medical Research and Development Command.

COMPLETED
Registry status
Phase 2
Development phase
35 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine whether Malarone ®, which is a drug approved to prevent malaria when taken daily, will still effectively prevent malaria if taken weekly.

Conditions Studied

Interventions

  • DRUG Atovaquone Proguanil
  • OTHER Procedure - malaria challenge

Study Locations (1)

Maryland

  • Walter Reed Army Institute of Research - Silver Spring

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2009-09
Est. Completion 2010-04
Phase Phase 2

What the Registry Record Tells You About NCT00984256

The ClinicalTrials.gov registry entry for NCT00984256 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 257-participant average among 27 other Malaria trials with a reported enrollment target (86% lower). The listed sponsor is U.S. Army Medical Research and Development Command, which has 77 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Malaria appearing as the primary indexed condition, and to 2 interventions - of which Atovaquone Proguanil is the first listed.

NCT00984256 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT00984256 about?

NCT00984256 is a clinical study titled "Weekly Dosing of Malarone ® for Prevention of Malaria". The purpose of this study is to determine whether Malarone ®, which is a drug approved to prevent malaria when taken daily, will still effectively prevent malaria if taken weekly.

What is the current status of trial NCT00984256?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 35 participants. The study started on 2009-09. Estimated completion is 2010-04.

What conditions does trial NCT00984256 study?

This clinical trial studies the following conditions: Malaria.

What interventions are being tested in trial NCT00984256?

The interventions under investigation include: Atovaquone Proguanil (DRUG), Procedure - malaria challenge (OTHER).

Who is sponsoring clinical trial NCT00984256?

This trial is sponsored by U.S. Army Medical Research and Development Command, which has 77 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00984256 being conducted?

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

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

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