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NCT02762123 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess the Effect of BMS-986142 on Pharmacokinetics (PK) of Probe Substrates

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

Completed
Registry status
Phase 1
Development phase
28
Enrollment target

NCT02762123: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT02762123 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 28 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02762123, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
28 participants
Enrollment target

Study Summary

The study is being conducted to assess the effect of BMS-986142 on the single-dose PK parameters of montelukast, flurbiprofen, omeprazole, midazolam, and digoxin, probe drugs for (cytochome P450) CYP2C8, CYP2C9, CYP2C19, CYP3A4, and P-glycoprotein (P-gp), respectively.

Interventions

  • DRUG BMS-986142 200mg
  • DRUG BMS Drug-drug interaction cocktail (montelukast, flurbiprofen, omeprazole, midazolam, and digoxin)
  • DRUG BMS-986142 350mg

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2016-05
Est. Completion 2016-08
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT02762123 record still lists

NCT02762123 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% lower).

The record links to 0 conditions, and to 3 interventions - of which BMS-986142 200mg is the first listed.

NCT02762123 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02762123 about?

NCT02762123 is a clinical study titled "A Study to Assess the Effect of BMS-986142 on Pharmacokinetics (PK) of Probe Substrates". The study is being conducted to assess the effect of BMS-986142 on the single-dose PK parameters of montelukast, flurbiprofen, omeprazole, midazolam, and digoxin, probe drugs for (cytochome P450) CYP2C8, CYP2C9, CYP2C19, CYP3A4, and P-glycoprotein (P-gp), respectively.

What is the current status of trial NCT02762123?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2016-05. Estimated completion is 2016-08.

What interventions are being tested in trial NCT02762123?

The interventions under investigation include: BMS-986142 200mg (DRUG), BMS Drug-drug interaction cocktail (montelukast, flurbiprofen, omeprazole, midazolam, and digoxin) (DRUG), BMS-986142 350mg (DRUG).

Who is sponsoring clinical trial NCT02762123?

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 NCT02762123's enrollment target sits among peer trials

28 1447th of 2000 higher than 538 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 NCT02762123, the US trial registry maintained by the National Library of Medicine. NCT02762123 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.