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NCT02031666 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess the Relative Bioavailability of 7 Test Tablet Formulations of JNJ-56021927 With Respect to the Capsule Formulation of JNJ-56021927 in Healthy Male Participants

A Phase 1 study, sponsored by Aragon Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
120
Enrollment target

NCT02031666: Completed Phase 1 study, sponsored by Aragon Pharmaceuticals.

NCT02031666 is a Phase 1 study that has completed, run by Aragon Pharmaceuticals. The registered enrollment target is 120 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (100% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02031666, a Phase 1 study, has completed, sponsored by Aragon Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
120 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the pharmacokinetics (what the body does to the medication) and relative bioavailability (the extent to which a medication or other substance becomes available to the body) of JNJ-56021927 when administered as 7 test tablet formulations of JNJ-56021927 compared with the softgel capsule formulation of JNJ-56021927 in healthy male participants under fasted conditions at a single dose of 240 mg.

Primary Outcome

The Plasma Concentration (Cmax) is defined as maximum observed analyte concentration.

Interventions

  • DRUG JNJ-56021927 capsule
  • DRUG JNJ-56021927 tablet

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2013-12
Est. Completion 2014-04
Phase Phase 1
Aragon Pharmaceuticals

12 total trials

What the finished NCT02031666 record still lists

NCT02031666 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (100% higher).

The record links to 0 conditions, and to 2 interventions - of which JNJ-56021927 capsule is the first listed.

NCT02031666 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02031666 about?

NCT02031666 is a clinical study titled "A Study to Assess the Relative Bioavailability of 7 Test Tablet Formulations of JNJ-56021927 With Respect to the Capsule Formulation of JNJ-56021927 in Healthy Male Participants". The purpose of this study is to evaluate the pharmacokinetics (what the body does to the medication) and relative bioavailability (the extent to which a medication or other substance becomes available to the body) of JNJ-56021927 when administered as 7 test tablet formulations of JNJ-56021927 compar...

What is the current status of trial NCT02031666?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 120 participants. The study started on 2013-12. Estimated completion is 2014-04.

What interventions are being tested in trial NCT02031666?

The interventions under investigation include: JNJ-56021927 capsule (DRUG), JNJ-56021927 tablet (DRUG).

Who is sponsoring clinical trial NCT02031666?

This trial is sponsored by Aragon Pharmaceuticals, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02031666's enrollment target sits among peer trials

120 479th of 2000 higher than 1,503 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 NCT02031666, the US trial registry maintained by the National Library of Medicine. NCT02031666 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.