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NCT04949269 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Drug Levels of Deucravacitinib From Tablets After Oral Administration in Healthy Participants

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

Completed
Registry status
Phase 1
Development phase
61
Enrollment target

NCT04949269: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT04949269 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 61 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04949269, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
61 participants
Enrollment target

Study Summary

The purpose of this study is to assess the drug levels of deucravacitinib after oral administration in healthy participants.

Interventions

  • DRUG Deucravacitinib
  • DRUG Famotidine

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2021-07-20
Est. Completion 2022-01-03
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT04949269 record still lists

NCT04949269 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 61 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

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

NCT04949269 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04949269 about?

NCT04949269 is a clinical study titled "A Study to Evaluate the Drug Levels of Deucravacitinib From Tablets After Oral Administration in Healthy Participants". The purpose of this study is to assess the drug levels of deucravacitinib after oral administration in healthy participants.

What is the current status of trial NCT04949269?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 61 participants. The study started on 2021-07-20. Estimated completion is 2022-01-03.

What interventions are being tested in trial NCT04949269?

The interventions under investigation include: Deucravacitinib (DRUG), Famotidine (DRUG).

Who is sponsoring clinical trial NCT04949269?

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 NCT04949269's enrollment target sits among peer trials

61 828th of 2000 higher than 1,170 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 NCT04949269, the US trial registry maintained by the National Library of Medicine. NCT04949269 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.