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NCT06716879 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of a Single Dose of Donzakimig in Healthy Chinese and Japanese Participants
A Phase 1 study of Healthy Participants, sponsored by UCB Biopharma SRL.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
- 1
- Study location
NCT06716879: Completed Phase 1 study of Healthy Participants, sponsored by UCB Biopharma SRL.
NCT06716879 is a Phase 1 study of Healthy Participants that has completed, run by UCB Biopharma SRL. The registered enrollment target is 32 participants, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (51% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06716879, a Phase 1 study of Healthy Participants, has completed, sponsored by UCB Biopharma SRL.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of the study is to investigate the safety, tolerability, and pharmacokinetic parameters of 2 dose strengths of donzakimig, each administered subcutaneously as a single dose, in healthy Chinese and Japanese study participants.
Primary Outcome
An Adverse Event (AE) is any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product, which does not necessarily have a causal relationship with this treatment. Treatment emergent adverse events (TEAEs) are adverse events not present prior to the pharmaceutical product administration or an already present event that worsens either in intensity or frequency
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Donzakimig
Study Locations (1)
California
- UP0142 1 - Anaheim
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2024-12-06 |
| Est. Completion | 2025-04-04 |
| Phase | Phase 1 |
What the finished NCT06716879 record still lists
NCT06716879 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (51% lower).
The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT06716879 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT06716879 about?
NCT06716879 is a clinical study titled "A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of a Single Dose of Donzakimig in Healthy Chinese and Japanese Participants". The purpose of the study is to investigate the safety, tolerability, and pharmacokinetic parameters of 2 dose strengths of donzakimig, each administered subcutaneously as a single dose, in healthy Chinese and Japanese study participants.
What is the current status of trial NCT06716879?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2024-12-06. Estimated completion is 2025-04-04.
What conditions does trial NCT06716879 study?
This clinical trial studies the following conditions: Healthy Participants.
What interventions are being tested in trial NCT06716879?
The interventions under investigation include: Placebo (DRUG), Donzakimig (DRUG).
Who is sponsoring clinical trial NCT06716879?
This trial is sponsored by UCB Biopharma SRL, which has 82 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06716879 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Healthy Participants
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06716879's enrollment target sits among peer trials
32 66th of 119 higher than 51 of 119 other Healthy Participants trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Healthy Participants 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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