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NCT06254664 · ClinicalTrials.gov registry record · Phase 1
Open Label Study to Assess the Effect of Patient Use and Robustness of Tiotropium 18ug Inhalation Powder, Hard Capsule,Zephir Inhaler Device
A Phase 1 study, sponsored by Xiromed.
- Completed
- Registry status
- Phase 1
- Development phase
- 116
- Enrollment target
NCT06254664: Completed Phase 1 study, sponsored by Xiromed.
NCT06254664 is a Phase 1 study that has completed, run by Xiromed. The registered enrollment target is 116 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06254664, a Phase 1 study, has completed, sponsored by Xiromed.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 116 participants
- Enrollment target
Study Summary
An Open Label Study to Assess the Effect of Patient Use and Robustness of Tiotropium 18ug Inhalation Powder, Hard Capsule, Inhaler Device. Zephir inhaler robustness will be assessed by in vitro testing of the Zephir inhaler after 12 weeks of patient use
Interventions
- DRUG Tiotropium 18 µg inhalation powder, hard capsule
- DEVICE Zephir inhaler
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 116 participants |
| Start Date | 2022-10-03 |
| Est. Completion | 2023-10-27 |
| Phase | Phase 1 |
What the finished NCT06254664 record still lists
NCT06254664 is an interventional study that assigns participants to a tested intervention. The registered 116 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% higher).
The record links to 0 conditions, and to 2 interventions - of which Tiotropium 18 µg inhalation powder, hard capsule is the first listed.
NCT06254664 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06254664 about?
NCT06254664 is a clinical study titled "Open Label Study to Assess the Effect of Patient Use and Robustness of Tiotropium 18ug Inhalation Powder, Hard Capsule,Zephir Inhaler Device". An Open Label Study to Assess the Effect of Patient Use and Robustness of Tiotropium 18ug Inhalation Powder, Hard Capsule, Inhaler Device. Zephir inhaler robustness will be assessed by in vitro testing of the Zephir inhaler after 12 weeks of patient use
What is the current status of trial NCT06254664?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 116 participants. The study started on 2022-10-03. Estimated completion is 2023-10-27.
What interventions are being tested in trial NCT06254664?
The interventions under investigation include: Tiotropium 18 µg inhalation powder, hard capsule (DRUG), Zephir inhaler (DEVICE).
Who is sponsoring clinical trial NCT06254664?
This trial is sponsored by Xiromed, which has 2 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06254664's enrollment target sits among peer trials
116 501st of 2000 higher than 1,497 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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