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

NCT03956680 · ClinicalTrials.gov registry record · Phase 1

An Investigational Immunotherapy Study of BMS-986301 Alone or in Combination With Nivolumab, and Ipilimumab in Participants With Advanced Solid Cancers

A Phase 1 study of Advanced Solid Cancers, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
54
Enrollment target
5
Study locations

NCT03956680: Completed Phase 1 study of Advanced Solid Cancers, sponsored by Bristol-Myers Squibb.

NCT03956680 is a Phase 1 study of Advanced Solid Cancers that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 54 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% lower). The trial reports 5 study locations across 5 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03956680, a Phase 1 study of Advanced Solid Cancers, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
54 participants
Enrollment target
5
Study locations

Study Summary

The main purpose of this study is to characterize the safety, tolerability, dose limiting toxicities, best route of administration, maximum tolerated dose, maximum administered dose, or alternative dose of BMS-986301 alone or in combination with nivolumab and ipilimumab in participants with cancers that have failed to respond to T cell checkpoint inhibiting antibodies.

Conditions Studied

Interventions

  • BIOLOGICAL Nivolumab
  • BIOLOGICAL Ipilimumab
  • DRUG BMS-986301

Study Locations (5)

Illinois

  • Local Institution - 0003 - Chicago

Missouri

  • Local Institution - 0005 - St Louis

Pennsylvania

  • Local Institution - 0006 - Pittsburgh

Tennessee

  • Local Institution - 0002 - Nashville

Ontario

  • Local Institution - 0001 - Toronto

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2019-03-26
Est. Completion 2024-04-24
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT03956680 record still lists

NCT03956680 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% lower).

The record links to 1 condition, with Advanced Solid Cancers appearing as the primary indexed condition, and to 3 interventions - of which Nivolumab is the first listed.

NCT03956680 lists 5 locations in 5 states (Illinois, Missouri, Pennsylvania).

Frequently Asked Questions

What is clinical trial NCT03956680 about?

NCT03956680 is a clinical study titled "An Investigational Immunotherapy Study of BMS-986301 Alone or in Combination With Nivolumab, and Ipilimumab in Participants With Advanced Solid Cancers". The main purpose of this study is to characterize the safety, tolerability, dose limiting toxicities, best route of administration, maximum tolerated dose, maximum administered dose, or alternative dose of BMS-986301 alone or in combination with nivolumab and ipilimumab in participants with cancers ...

What is the current status of trial NCT03956680?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2019-03-26. Estimated completion is 2024-04-24.

What conditions does trial NCT03956680 study?

This clinical trial studies the following conditions: Advanced Solid Cancers.

What interventions are being tested in trial NCT03956680?

The interventions under investigation include: Nivolumab (BIOLOGICAL), Ipilimumab (BIOLOGICAL), BMS-986301 (DRUG).

Who is sponsoring clinical trial NCT03956680?

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

Where is trial NCT03956680 being conducted?

This trial has 5 study locations across Illinois, Missouri, Pennsylvania, Tennessee, Ontario. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Advanced Solid Cancers

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03956680's enrollment target sits among peer trials

54 931st of 2000 higher than 1,053 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01269853 · 54 participants · Phase 1

    Repeated Super-selective Intraarterial Cerebral Infusion of Bevacizumab (Avastin) for Treatment of Relapsed GBM and AA

  • NCT02390752 · 54 participants · Phase 1

    Phase I Trial of TURALIO(R) (Pexidartinib, PLX3397) in Children and Young Adults With Refractory Leukemias and Refractory Solid Tumors Including Neurofibromatosis Type 1 (NF1) Associated Plexiform Neurofibromas (PN) and Tenosynovial Giant Cell Tumor ...

  • NCT02991248 · 54 participants · NA

    Improve Dynamic Lateral Balance of Humans With SCI

  • NCT02993900 · 54 participants · NA

    Image-Guided Gynecologic Brachytherapy

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03956680, the US trial registry maintained by the National Library of Medicine. NCT03956680 (small enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.