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NCT02930694 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate the Bioavailability, Safety and Tolerability of a Solid Dosage Formulation Relative to a Suspension of JNJ-54175446 in Healthy Male and Female Participants
A Phase 1 study, sponsored by Janssen Research & Development.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
NCT02930694: Completed Phase 1 study, sponsored by Janssen Research & Development.
NCT02930694 is a Phase 1 study that has completed, run by Janssen Research & Development. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02930694, a Phase 1 study, has completed, sponsored by Janssen Research & Development.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
Study Summary
The primary purpose of the study is to investigate the plasma pharmacokinetics and bioavailability (BA) of a single dose of a solid dose formulation with 2 different strengths of JNJ-54175446 (50 milligram \[mg\] and 100 mg capsules) relative to the suspension of JNJ-54175446 under fasting conditions.
Primary Outcome
The Cmax is the maximum observed plasma concentration.
Interventions
- DRUG JNJ-54175446 (capsule)
- DRUG JNJ-54175446 (suspension)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2016-10 |
| Est. Completion | 2016-12 |
| Phase | Phase 1 |
What the finished NCT02930694 record still lists
NCT02930694 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 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).
The record links to 0 conditions, and to 2 interventions - of which JNJ-54175446 (capsule) is the first listed.
NCT02930694 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02930694 about?
NCT02930694 is a clinical study titled "A Study to Evaluate the Bioavailability, Safety and Tolerability of a Solid Dosage Formulation Relative to a Suspension of JNJ-54175446 in Healthy Male and Female Participants". The primary purpose of the study is to investigate the plasma pharmacokinetics and bioavailability (BA) of a single dose of a solid dose formulation with 2 different strengths of JNJ-54175446 (50 milligram \[mg\] and 100 mg capsules) relative to the suspension of JNJ-54175446 under fasting condition...
What is the current status of trial NCT02930694?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2016-10. Estimated completion is 2016-12.
What interventions are being tested in trial NCT02930694?
The interventions under investigation include: JNJ-54175446 (capsule) (DRUG), JNJ-54175446 (suspension) (DRUG).
Who is sponsoring clinical trial NCT02930694?
This trial is sponsored by Janssen Research & Development, which has 593 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02930694's enrollment target sits among peer trials
32 1296th of 2000 higher than 679 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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