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NCT07220551 · ClinicalTrials.gov registry record · Phase 1

A Phase 1 Relative Bioavailability Study of UCB0022 Tablets in Healthy Participants

A Phase 1 study, sponsored by UCB Biopharma SRL.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target

NCT07220551: Completed Phase 1 study, sponsored by UCB Biopharma SRL.

NCT07220551 is a Phase 1 study that has completed, run by UCB Biopharma SRL. The registered enrollment target is 14 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07220551, a Phase 1 study, has completed, sponsored by UCB Biopharma SRL.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target

Study Summary

The purpose of this study is to estimate the relative bioavailability of UCB0022 Formulation 2 (Test) versus Formulation 1 (Reference) in healthy participants following single oral administration.

Primary Outcome

AUC: Area under the plasma concentration-time curve.

Interventions

  • DRUG UCB0022

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2025-10-23
Est. Completion 2025-12-16
Phase Phase 1
UCB Biopharma SRL

82 total trials

What the finished NCT07220551 record still lists

NCT07220551 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 1 intervention - of which UCB0022 is the first listed.

NCT07220551 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07220551 about?

NCT07220551 is a clinical study titled "A Phase 1 Relative Bioavailability Study of UCB0022 Tablets in Healthy Participants". The purpose of this study is to estimate the relative bioavailability of UCB0022 Formulation 2 (Test) versus Formulation 1 (Reference) in healthy participants following single oral administration.

What is the current status of trial NCT07220551?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2025-10-23. Estimated completion is 2025-12-16.

What interventions are being tested in trial NCT07220551?

The interventions under investigation include: UCB0022 (DRUG).

Who is sponsoring clinical trial NCT07220551?

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 NCT07220551's enrollment target sits among peer trials

14 1844th of 2000 higher than 154 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 NCT07220551, the US trial registry maintained by the National Library of Medicine. NCT07220551 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.