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NCT04175925 · ClinicalTrials.gov registry record · Phase 1
A Study Assessing the Drug Levels, Drug Effects, and Safety of BMS-986322 in Healthy Participants
A Phase 1 study of Healthy Participants, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 171
- Enrollment target
- 1
- Study location
NCT04175925 is a Phase 1 study of Healthy Participants that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 171 participants, above the 64-participant average among 119 other Healthy Participants trials with a reported enrollment target (167% higher). The trial reports 1 study location across 1 state.
The verdict
NCT04175925, a Phase 1 study of Healthy Participants, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 171 participants
- Enrollment target
- 1
- Study location
Study Summary
A Study assessing the drug levels and drug effects of variable doses of BMS-986322 in Healthy Participants compared to a placebo. The study also assesses how BMS-986322 affects the body with food and its acidity levels.
Conditions Studied
Interventions
- DRUG famotidine
- DRUG BMS-986322
- OTHER BMS-986322 Placebo
Study Locations (1)
Kansas
- ICON (LPRA) - Lenexa - Lenexa
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 171 participants |
| Start Date | 2019-11-15 |
| Est. Completion | 2021-07-13 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04175925
The ClinicalTrials.gov registry entry for NCT04175925 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 171 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 64-participant average among 119 other Healthy Participants trials with a reported enrollment target (167% higher). The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 3 interventions - of which famotidine is the first listed.
NCT04175925 reports 1 study location spanning 1 distinct geographic area - top geographies include Kansas.
Frequently Asked Questions
What is clinical trial NCT04175925 about?
NCT04175925 is a clinical study titled "A Study Assessing the Drug Levels, Drug Effects, and Safety of BMS-986322 in Healthy Participants". A Study assessing the drug levels and drug effects of variable doses of BMS-986322 in Healthy Participants compared to a placebo. The study also assesses how BMS-986322 affects the body with food and its acidity levels.
What is the current status of trial NCT04175925?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 171 participants. The study started on 2019-11-15. Estimated completion is 2021-07-13.
What conditions does trial NCT04175925 study?
This clinical trial studies the following conditions: Healthy Participants.
What interventions are being tested in trial NCT04175925?
The interventions under investigation include: famotidine (DRUG), BMS-986322 (DRUG), BMS-986322 Placebo (OTHER).
Who is sponsoring clinical trial NCT04175925?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04175925 being conducted?
This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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.