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NCT03369223 · ClinicalTrials.gov registry record · Phase 1

A Study of BMS-986249 Alone and in Combination With Nivolumab in Advanced Solid Tumors

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

Completed
Registry status
Phase 1
Development phase
356
Enrollment target

NCT03369223: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT03369223 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 356 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (493% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03369223, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
356 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether BMS-986249 both by itself and in combination with Nivolumab is safe and tolerable in the treatment of advanced solid tumors

Primary Outcome

Adverse Events (AEs): Adverse events are any unwanted or harmful medical occurrences in a participant who receives a study drug or intervention. These events may or may not be related to the treatment. Serious Adverse Events (SAEs): Serious adverse events are adverse events that result in death, are life-threatening, require hospitalization or prolong existing hospitalization, cause significant disability or incapacity, or result in a birth defect.

Interventions

  • BIOLOGICAL Nivolumab
  • BIOLOGICAL Ipilimumab
  • BIOLOGICAL BMS-986249

Trial Details

FieldValue
Enrollment Target 356 participants
Start Date 2017-12-06
Est. Completion 2024-11-07
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT03369223 record still lists

NCT03369223 is an interventional study that assigns participants to a tested intervention. The registered 356 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (493% higher).

The record links to 0 conditions, and to 3 interventions - of which Nivolumab is the first listed.

NCT03369223 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03369223 about?

NCT03369223 is a clinical study titled "A Study of BMS-986249 Alone and in Combination With Nivolumab in Advanced Solid Tumors". The purpose of this study is to determine whether BMS-986249 both by itself and in combination with Nivolumab is safe and tolerable in the treatment of advanced solid tumors

What is the current status of trial NCT03369223?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 356 participants. The study started on 2017-12-06. Estimated completion is 2024-11-07.

What interventions are being tested in trial NCT03369223?

The interventions under investigation include: Nivolumab (BIOLOGICAL), Ipilimumab (BIOLOGICAL), BMS-986249 (BIOLOGICAL).

Who is sponsoring clinical trial NCT03369223?

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 NCT03369223's enrollment target sits among peer trials

356 95th of 2000 higher than 1,906 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 NCT03369223, the US trial registry maintained by the National Library of Medicine. NCT03369223 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.