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NCT04136444 · ClinicalTrials.gov registry record · Phase 1
A Pharmacokinetic Study of Padsevonil in Study Participants With Either Normal or Moderately Impaired Hepatic Function
A Phase 1 study, sponsored by UCB Biopharma S.P.R.L..
- Terminated
- Registry status
- Phase 1
- Development phase
- 12
- Enrollment target
NCT04136444: Clinical Trial Phase 1 study, sponsored by UCB Biopharma S.P.R.L..
NCT04136444 is a Phase 1 study that was terminated before completion, run by UCB Biopharma S.P.R.L.. 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
NCT04136444, a Phase 1 study, was terminated before completion, sponsored by UCB Biopharma S.P.R.L..
- TERMINATED
- Registry status
- Phase 1
- Development phase
- 12 participants
- Enrollment target
Study Summary
The purpose of the study is to evaluate the plasma pharmacokinetic (PK), safety and tolerability of padsevonil (PSL) in hepatically impaired and non-hepatically impaired study participants.
Primary Outcome
Cmax is maximum observed plasma concentration.
Interventions
- DRUG Padsevonil
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2019-10-28 |
| Est. Completion | 2020-05-22 |
| Phase | Phase 1 |
Why NCT04136444 stopped before completion
NCT04136444 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 1 intervention - of which Padsevonil is the first listed.
NCT04136444 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04136444 about?
NCT04136444 is a clinical study titled "A Pharmacokinetic Study of Padsevonil in Study Participants With Either Normal or Moderately Impaired Hepatic Function". The purpose of the study is to evaluate the plasma pharmacokinetic (PK), safety and tolerability of padsevonil (PSL) in hepatically impaired and non-hepatically impaired study participants.
What is the current status of trial NCT04136444?
This trial is currently terminated. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2019-10-28. Estimated completion is 2020-05-22.
What interventions are being tested in trial NCT04136444?
The interventions under investigation include: Padsevonil (DRUG).
Who is sponsoring clinical trial NCT04136444?
This trial is sponsored by UCB Biopharma S.P.R.L., which has 23 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04136444'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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