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NCT05626439 · ClinicalTrials.gov registry record · Phase 1

A Relative Bioavailability Study of Staccato Alprazolam Versus Oral Alprazolam in Healthy Study Participants

A Phase 1 study, sponsored by UCB Biopharma SRL.

Completed
Registry status
Phase 1
Development phase
21
Enrollment target

NCT05626439: Completed Phase 1 study, sponsored by UCB Biopharma SRL.

NCT05626439 is a Phase 1 study that has completed, run by UCB Biopharma SRL. The registered enrollment target is 21 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05626439, a Phase 1 study, has completed, sponsored by UCB Biopharma SRL.

COMPLETED
Registry status
Phase 1
Development phase
21 participants
Enrollment target

Study Summary

The purpose of the study is to evaluate the relative bioavailability of alprazolam in plasma following a single dose of Staccato alprazolam compared to a single dose of oral alprazolam under fasted conditions

Primary Outcome

AUC = Area under the plasma concentration-time curve from time zero to infinity

Interventions

  • DRUG Staccato alprazolam
  • DRUG Oral alprazolam

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2022-12-28
Est. Completion 2023-02-24
Phase Phase 1
UCB Biopharma SRL

82 total trials

What the finished NCT05626439 record still lists

NCT05626439 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower).

The record links to 0 conditions, and to 2 interventions - of which Staccato alprazolam is the first listed.

NCT05626439 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05626439 about?

NCT05626439 is a clinical study titled "A Relative Bioavailability Study of Staccato Alprazolam Versus Oral Alprazolam in Healthy Study Participants". The purpose of the study is to evaluate the relative bioavailability of alprazolam in plasma following a single dose of Staccato alprazolam compared to a single dose of oral alprazolam under fasted conditions

What is the current status of trial NCT05626439?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2022-12-28. Estimated completion is 2023-02-24.

What interventions are being tested in trial NCT05626439?

The interventions under investigation include: Staccato alprazolam (DRUG), Oral alprazolam (DRUG).

Who is sponsoring clinical trial NCT05626439?

This trial is sponsored by UCB Biopharma SRL, which has 82 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05626439's enrollment target sits among peer trials

21 1615th of 2000 higher than 372 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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Source: ClinicalTrials.gov NCT05626439, the US trial registry maintained by the National Library of Medicine. NCT05626439 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.