Evaluation of Azithromycin-Chloroquine Combination to Prevent Malaria with Weekly Dosing

Abstract

Malaria remains the top infectious disease threat facing the U.S. military in many forward operating environments. Current FDA approved weekly chemoprophylaxis options have contraindications that can limit prescribing. In this open label study 18 healthy volunteers, aged 18-50 years (inclusive), were randomly assigned to receive either 300 mg CQ or 300 mg CQ and 2 gm azithromycin (CQAZ) of directly observed therapy, weekly for 3 weeks prior to undergoing mosquito bite challenge with chloroquine-resistant Plasmodium falciparum. The primary objective of this study was to assess the safety and efficacy of a weekly CQAZ regimen for prophylaxis against CQ resistant Plasmodium falciparum. Secondary objectives were to assess the tolerability and pharmacokinetics of the regimen. Given the high rate of side effects and poor efficacy when administered for 3 weeks before and after challenge, the combination of weekly chloroquine and azithromycin is a suboptimal regimen combination for weekly malaria chemoprophylaxis.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 2020
Accession Number
AD1118219

Entities

People

  • Jeffrey Livezey

Organizations

  • Uniformed Services University of the Health Sciences
  • Walter Reed Army Institute of Research

Tags

DTIC Thesaurus Topics

  • Anti-Infective Agents
  • Antimalarials
  • Biomedical Research
  • Chemical Reactions
  • Department Of Defense
  • Diseases And Disorders
  • Governments
  • Health Services
  • Infection
  • Infectious Diseases
  • Liquid Chromatography
  • Malaria
  • Mass Spectrometry
  • Medical Personnel
  • Monitoring
  • Pain
  • Parasitic Diseases
  • Side Effects
  • Standards
  • Therapy
  • United States

Fields of Study

  • Medicine

Readers

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