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NCT06299709 · ClinicalTrials.gov registry record · Phase 1
A Study To Evaluate the Relative Bioavailability, Food Effect, and Dose Proportionality of a Granule Formulation of Vanzacaftor/Tezacaftor/Deutivacaftor(VNZ/TEZ/D-IVA)
A Phase 1 study, sponsored by Vertex Pharmaceuticals Incorporated.
- Completed
- Registry status
- Phase 1
- Development phase
- 34
- Enrollment target
NCT06299709: Completed Phase 1 study, sponsored by Vertex Pharmaceuticals Incorporated.
NCT06299709 is a Phase 1 study that has completed, run by Vertex Pharmaceuticals Incorporated. The registered enrollment target is 34 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (43% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06299709, a Phase 1 study, has completed, sponsored by Vertex Pharmaceuticals Incorporated.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 34 participants
- Enrollment target
Study 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.
Interventions
- DRUG VNZ/TEZ/D-IVA
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 34 participants |
| Start Date | 2024-03-13 |
| Est. Completion | 2024-05-23 |
| Phase | Phase 1 |
What the finished NCT06299709 record still lists
NCT06299709 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (43% lower).
The record links to 0 conditions, and to 1 intervention - of which VNZ/TEZ/D-IVA is the first listed.
NCT06299709 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06299709 about?
NCT06299709 is a clinical study titled "A Study To Evaluate the Relative Bioavailability, Food Effect, and Dose Proportionality of a Granule Formulation of Vanzacaftor/Tezacaftor/Deutivacaftor(VNZ/TEZ/D-IVA)". 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.
What is the current status of trial NCT06299709?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 34 participants. The study started on 2024-03-13. Estimated completion is 2024-05-23.
What interventions are being tested in trial NCT06299709?
The interventions under investigation include: VNZ/TEZ/D-IVA (DRUG).
Who is sponsoring clinical trial NCT06299709?
This trial is sponsored by Vertex Pharmaceuticals Incorporated, which has 191 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06299709's enrollment target sits among peer trials
34 1273rd of 2000 higher than 721 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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