drugset / Trial / NCT06299709
A Study To Evaluate the Relative Bioavailability, Food Effect, and Dose Proportionality of a Granule Formulation of Vanzacaftor/Tezacaftor/Deutivacaftor(VNZ/TEZ/D-IVA)
RandomizedCrossoverOpen-labelTreatment
Summary
The purpose of this study is to evaluate the relative bioavailability, food effect, and dose proportionality of a granule formulation of VNZ/TEZ/D-IVA.
Timeline
- Start
- 2024-03-13
- Primary completion
- 2024-05-23
- Completion
- 2024-05-23
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vanzacaftor | Small molecule | — | Oral |
| Subject | deutivacaftor | Unknown | — | Oral |
| Subject | tezacaftor | Other / unclassified | — | Oral |