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NCT02857777 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetic, Safety, and Tolerability Study of Intranasally Administered Esketamine in Elderly Japanese, and Healthy Younger Adult Japanese Subjects

A Phase 1 study, sponsored by Janssen Research & Development.

Completed
Registry status
Phase 1
Development phase
37
Enrollment target

NCT02857777: Completed Phase 1 study, sponsored by Janssen Research & Development.

NCT02857777 is a Phase 1 study that has completed, run by Janssen Research & Development. The registered enrollment target is 37 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02857777, a Phase 1 study, has completed, sponsored by Janssen Research & Development.

COMPLETED
Registry status
Phase 1
Development phase
37 participants
Enrollment target

Study Summary

The purpose of this study is to compare the pharmacokinetics, safety, and tolerability of intranasally administered esketamine in elderly Japanese subjects and healthy younger adult Japanese subjects.

Primary Outcome

The Cmax is the maximum plasma concentration.

Interventions

  • DRUG Esketamine

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2016-08-09
Est. Completion 2017-01-27
Phase Phase 1
Janssen Research & Development

593 total trials

What the finished NCT02857777 record still lists

NCT02857777 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% lower).

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

NCT02857777 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02857777 about?

NCT02857777 is a clinical study titled "Pharmacokinetic, Safety, and Tolerability Study of Intranasally Administered Esketamine in Elderly Japanese, and Healthy Younger Adult Japanese Subjects". The purpose of this study is to compare the pharmacokinetics, safety, and tolerability of intranasally administered esketamine in elderly Japanese subjects and healthy younger adult Japanese subjects.

What is the current status of trial NCT02857777?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 37 participants. The study started on 2016-08-09. Estimated completion is 2017-01-27.

What interventions are being tested in trial NCT02857777?

The interventions under investigation include: Esketamine (DRUG).

Who is sponsoring clinical trial NCT02857777?

This trial is sponsored by Janssen Research & Development, which has 593 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02857777's enrollment target sits among peer trials

37 1204th of 2000 higher than 791 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 NCT02857777, the US trial registry maintained by the National Library of Medicine. NCT02857777 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.