009/07; Bioequivalence Trial of Pyronaridine:Artesunate to-be-Marketed Tablet to the Clinical Trial Reference Tablet
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
The purpose of the study is to determine the bioequivalence of the combination of pyronaridine and artesunate (180:60mg) to-be-marketed tablet to the clinical trial reference tablet administered as a single total dose of 720:240 mg in healthy adults.
Description
The purpose of the study is to determine the bioequivalence of the combination of pyronaridine and artesunate (180:60mg) to-be-marketed tablet to the clinical trial reference tablet administered as a single total dose of 720:240 mg in healthy adults.
Details
| Condition | Malaria |
|---|---|
| Age | 18years - 45years |
| Clinical Study Identifier | TX4310 |
| Last Modified on | 19 February 2024 |
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