drugset / Trial / NCT02564471
Effect of Antimalarial Drugs to Rabies Vaccine for Post-exposure Prophylaxis.
Phase 4
Completed
103 enrolled
State University of New York - Upstate Medical University
Kansas State University · collabWalter Reed Army Institute of Research (WRAIR) · collab
RandomizedParallel-groupOpen-labelBasic science
Summary
This is an exploratory trial to evaluate the effect of antimalarial drugs on the immune response generated by rabies vaccine when administered for post-exposure prophylaxis. This study will use the FDA approved post-exposure prophylaxis vaccine regimen (without rabies immune globulin) in the presence or absence of an FDA-approved malaria chemoprophylaxis regimen.
Timeline
- Start
- 2016-11-11
- Primary completion
- 2018-08
- Completion
- 2019-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Atovaquone | Small molecule | 250 mg | Oral |
| Subject | Chloroquine | Small molecule | 500 mg | Oral |
| Subject | Doxycycline | Small molecule | 100 mg | Oral |
| Subject | Proguanil | Small molecule | 100 mg | Oral |
| Subject | Rabies vaccine | Vaccine | 1 ml | Intramuscular |
| Subject | Rabies vaccine | Vaccine | 2.5 iu | Intramuscular |