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COMPLETED Phase 1

An Investigational Immuno-therapy Study of Experimental Medication BMS-986156, Given by Itself or in Combination With Nivolumab in Patients With Solid Cancers or Cancers That Have Spread.

NCT02598960 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the safety and tumor-shrinking ability of experimental medication BMS-986156, when given by itself or in combination with nivolumab in patients with solid cancers that are advanced or cancers that have spread.

Conditions Studied

Interventions

  • DRUG Nivolumab
  • DRUG BMS-986156

Study Locations (20)

Other

  • Local Institution - 0012 — Ghent
  • Local Institution — Paris
  • Institut Claudius Regaud — Toulouse
  • Institut Gustave Roussy — Vlllejuif
  • Local Institution — Bonn
  • Local Institution — Freiburg im Breisgau
  • Local Institution — Würzburg

New South Wales

  • Liverpool Cancer Therapy Center — Liverpool
  • Local Institution — Westmead

Alabama

  • University Of Alabama At Birmingham — Birmingham

California

  • UCSD Moores Cancer Center — La Jolla

Georgia

  • Emory University — Atlanta

Ohio

  • The Ohio State University — Columbus

Oregon

  • Providence Portland Medical Center — Portland

Pennsylvania

  • Thomas Jefferson University Hospital — Philadelphia

Trial Details

FieldValue
Enrollment Target 295 participants
Start Date 2015-10-14
Est. Completion 2019-12-16
Phase Phase 1

Sponsor

Bristol-Myers Squibb

504 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02598960

The ClinicalTrials.gov registry entry for NCT02598960 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 295 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 504 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 2 interventions — of which Nivolumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02598960 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Other, New South Wales, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02598960 about?

NCT02598960 is a clinical study titled "An Investigational Immuno-therapy Study of Experimental Medication BMS-986156, Given by Itself or in Combination With Nivolumab in Patients With Solid Cancers or Cancers That Have Spread.". The purpose of this study is to evaluate the safety and tumor-shrinking ability of experimental medication BMS-986156, when given by itself or in combination with nivolumab in patients with solid cancers that are advanced or cancers that have spread.

What is the current status of trial NCT02598960?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 295 participants. The study started on 2015-10-14. Estimated completion is 2019-12-16.

What conditions does trial NCT02598960 study?

This clinical trial studies the following conditions: Solid Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02598960?

The interventions under investigation include: Nivolumab (DRUG), BMS-986156 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02598960?

This trial is sponsored by Bristol-Myers Squibb, which has 504 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02598960 being conducted?

This trial has 20 study locations across Alabama, California, Georgia, Ohio, Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial