Single-dose study testing a rivaroxaban dry powder formulation for oral suspension in children from 6 months to 12 years with previous thrombosis
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
The purpose of this study is to evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) of oral liquid rivaroxaban and to assess the safety and tolerability.
Description
The purpose of this study is to evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) of oral liquid rivaroxaban and to assess the safety and tolerability.
Details
| Condition | thrombosis |
|---|---|
| Age | 100years or below |
| Clinical Study Identifier | TX5533 |
| Last Modified on | 19 February 2024 |
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