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NCT05625412 · ClinicalTrials.gov registry record · Phase 1

A Study of BMS-986360/CC-90001 Alone and in Combination With Chemotherapy or Nivolumab in Advanced Solid Tumors

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

Completed
Registry status
Phase 1
Development phase
70
Enrollment target

NCT05625412: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT05625412 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 70 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05625412, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
70 participants
Enrollment target

Study Summary

The aim of this study is to assess the safety and tolerability of BMS-986360 as monotherapy and in combination with chemotherapy or nivolumab in participants with advanced solid tumors.

Interventions

  • DRUG Docetaxel
  • DRUG Capecitabine
  • DRUG Nivolumab
  • DRUG BMS-986360

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2022-12-09
Est. Completion 2025-05-12
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT05625412 record still lists

NCT05625412 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% higher).

The record links to 0 conditions, and to 4 interventions - of which Docetaxel is the first listed.

NCT05625412 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05625412 about?

NCT05625412 is a clinical study titled "A Study of BMS-986360/CC-90001 Alone and in Combination With Chemotherapy or Nivolumab in Advanced Solid Tumors". The aim of this study is to assess the safety and tolerability of BMS-986360 as monotherapy and in combination with chemotherapy or nivolumab in participants with advanced solid tumors.

What is the current status of trial NCT05625412?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 70 participants. The study started on 2022-12-09. Estimated completion is 2025-05-12.

What interventions are being tested in trial NCT05625412?

The interventions under investigation include: Docetaxel (DRUG), Capecitabine (DRUG), Nivolumab (DRUG), BMS-986360 (DRUG).

Who is sponsoring clinical trial NCT05625412?

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 NCT05625412's enrollment target sits among peer trials

70 749th of 2000 higher than 1,227 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 NCT05625412, the US trial registry maintained by the National Library of Medicine. NCT05625412 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.