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NCT03994601 · ClinicalTrials.gov registry record · Phase 1

An Investigational Immunotherapy Study of BMS-986288 Alone and in Combination With Nivolumab in Advanced Solid Cancers

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

Completed
Registry status
Phase 1
Development phase
219
Enrollment target

NCT03994601: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT03994601 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 219 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (265% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03994601, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
219 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether BMS-986288 both by itself and in combination with Nivolumab is safe and tolerable in the treatment of select advanced solid tumors.

Primary Outcome

Safety releated events for Cohorts 1A, 1B and 2B.

Interventions

  • DRUG Nivolumab
  • DRUG Regorafenib
  • DRUG BMS-986288

Trial Details

FieldValue
Enrollment Target 219 participants
Start Date 2019-09-06
Est. Completion 2024-08-31
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT03994601 record still lists

NCT03994601 is an interventional study that assigns participants to a tested intervention. The registered 219 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 (265% higher).

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

NCT03994601 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03994601 about?

NCT03994601 is a clinical study titled "An Investigational Immunotherapy Study of BMS-986288 Alone and in Combination With Nivolumab in Advanced Solid Cancers". The purpose of this study is to determine whether BMS-986288 both by itself and in combination with Nivolumab is safe and tolerable in the treatment of select advanced solid tumors.

What is the current status of trial NCT03994601?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 219 participants. The study started on 2019-09-06. Estimated completion is 2024-08-31.

What interventions are being tested in trial NCT03994601?

The interventions under investigation include: Nivolumab (DRUG), Regorafenib (DRUG), BMS-986288 (DRUG).

Who is sponsoring clinical trial NCT03994601?

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 NCT03994601's enrollment target sits among peer trials

219 238th of 2000 higher than 1,762 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 NCT03994601, the US trial registry maintained by the National Library of Medicine. NCT03994601 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.