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NCT04848662 · ClinicalTrials.gov registry record · Phase 1
To Compare the Pharmacokinetics of Budesonide Delivered by BDA MDI to Budesonide Delivered by Pulmicort Respules in Children With Asthma Aged 4 to 8 Years.
A Phase 1 study, sponsored by Bond Avillion 2 Development.
- Completed
- Registry status
- Phase 1
- Development phase
- 12
- Enrollment target
NCT04848662: Completed Phase 1 study, sponsored by Bond Avillion 2 Development.
NCT04848662 is a Phase 1 study that has completed, run by Bond Avillion 2 Development. The registered enrollment target is 12 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04848662, a Phase 1 study, has completed, sponsored by Bond Avillion 2 Development.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 12 participants
- Enrollment target
Study Summary
To compare the pharmacokinetics of budesonide delivered by BDA MDI to budesonide delivered by Pulmicort Respules in children with Asthma aged 4 to 8 years.
Primary Outcome
Area under the plasma concentration-time curve from time zero to time of last quantifiable concentration
Interventions
- DRUG BDA MDI (PT027) 160/180 μg
- DRUG Pulmicort Respules 0.5 MG/ML Inhalation Suspension
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2021-05-06 |
| Est. Completion | 2021-07-08 |
| Phase | Phase 1 |
What the finished NCT04848662 record still lists
NCT04848662 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower).
The record links to 0 conditions, and to 2 interventions - of which BDA MDI (PT027) 160/180 μg is the first listed.
NCT04848662 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04848662 about?
NCT04848662 is a clinical study titled "To Compare the Pharmacokinetics of Budesonide Delivered by BDA MDI to Budesonide Delivered by Pulmicort Respules in Children With Asthma Aged 4 to 8 Years.". To compare the pharmacokinetics of budesonide delivered by BDA MDI to budesonide delivered by Pulmicort Respules in children with Asthma aged 4 to 8 years.
What is the current status of trial NCT04848662?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2021-05-06. Estimated completion is 2021-07-08.
What interventions are being tested in trial NCT04848662?
The interventions under investigation include: BDA MDI (PT027) 160/180 μg (DRUG), Pulmicort Respules 0.5 MG/ML Inhalation Suspension (DRUG).
Who is sponsoring clinical trial NCT04848662?
This trial is sponsored by Bond Avillion 2 Development, which has 6 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04848662's enrollment target sits among peer trials
12 1852nd of 2000 higher than 90 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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