Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04209699 · ClinicalTrials.gov registry record · Phase 1

A Study Comparing the Effects of Famotidine Pretreatment and of Food on the Relative Bioavailability of BMS-986165 in Healthy Volunteers

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

Completed
Registry status
Phase 1
Development phase
18
Enrollment target

NCT04209699 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 18 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04209699, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
18 participants
Enrollment target

Study Summary

The primary purpose of this study is to evaluate the effects of food and pH on the relative bioavailability (BA) of the tablet formulation of BMS-986165 in healthy volunteers

Interventions

  • DRUG BMS-986165
  • DRUG Famotidine

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2019-12-27
Est. Completion 2020-02-11
Phase Phase 1

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT04209699

The ClinicalTrials.gov registry entry for NCT04209699 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which BMS-986165 is the first listed.

NCT04209699 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04209699 about?

NCT04209699 is a clinical study titled "A Study Comparing the Effects of Famotidine Pretreatment and of Food on the Relative Bioavailability of BMS-986165 in Healthy Volunteers". The primary purpose of this study is to evaluate the effects of food and pH on the relative bioavailability (BA) of the tablet formulation of BMS-986165 in healthy volunteers

What is the current status of trial NCT04209699?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 18 participants. The study started on 2019-12-27. Estimated completion is 2020-02-11.

What interventions are being tested in trial NCT04209699?

The interventions under investigation include: BMS-986165 (DRUG), Famotidine (DRUG).

Who is sponsoring clinical trial NCT04209699?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.