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NCT02327273 · ClinicalTrials.gov registry record · Phase 1

Randomized, Placebo-Controlled, Double-Blind, Ascending Single and Multiple Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BMS-963272 in Healthy Subjects

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
88
Enrollment target

NCT02327273: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT02327273 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 88 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02327273, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
88 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety profile, tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) following single and multiple oral doses of BMS-963272 in healthy subjects.

Interventions

  • DRUG Placebo
  • DRUG BMS-963272

Trial Details

FieldValue
Enrollment Target 88 participants
Start Date 2014-10
Est. Completion 2015-05
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT02327273 record still lists

NCT02327273 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 88 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% higher).

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

NCT02327273 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02327273 about?

NCT02327273 is a clinical study titled "Randomized, Placebo-Controlled, Double-Blind, Ascending Single and Multiple Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BMS-963272 in Healthy Subjects". The purpose of this study is to evaluate the safety profile, tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) following single and multiple oral doses of BMS-963272 in healthy subjects.

What is the current status of trial NCT02327273?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 88 participants. The study started on 2014-10. Estimated completion is 2015-05.

What interventions are being tested in trial NCT02327273?

The interventions under investigation include: Placebo (DRUG), BMS-963272 (DRUG).

Who is sponsoring clinical trial NCT02327273?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02327273's enrollment target sits among peer trials

88 650th of 2000 higher than 1,350 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 NCT02327273, the US trial registry maintained by the National Library of Medicine. NCT02327273 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.