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NCT06544655Active, not recruitingPhase 1

A Study of BMS-986484 Alone and Combination Therapy in Participants With Advanced Solid Tumors

A Phase 1/1b First-in-human Trial of BMS-986484 as Monotherapy and Combination Therapy in Participants With Advanced Solid Malignancies

Source: ClinicalTrials.gov · Last updated 17 Apr 2026

Brief summary (registry, in English)

The purpose of this study is to assess the safety and tolerability of BMS-986484 administered alone, in combination with nivolumab in participants with advanced/metastatic solid tumors including non-small cell lung cancer (NSCLC), microsatellite stable (MSS) colorectal carcinoma (CRC), pancreatic ductal adenocarcinoma (PDAC), gastric/gastroesophageal junction adenocarcinoma (G/GEJC), and squamous cell carcinoma of the head and neck (SCCHN).

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
213 (estimated)
First submitted
5 Aug 2024
Start date
10 Oct 2024
Primary completion date
14 Oct 2027
Lead sponsor
Bristol-Myers Squibb
NCT number
NCT06544655
EudraCT number
2024-513696-40

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 213
  • From 10 Oct 2024 to the primary completion date, 14 Oct 2027
  • 9 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of or with active interstitial lung disease or pulmonary fibrosis.
  • Active, known, or suspected autoimmune disease.
  • Serious uncontrolled medical disorders.
  • New onset, non-catheter-associated venous thromboembolism within the past 6 months.

Other

  • Other protocol-defined Inclusion/Exclusion criteria apply.

Who the study is looking for

  • Locally advanced unresectable, metastatic, or recurrent malignant tumors including non-small cell lung cancer (NSCLC), pancreatic ductal adenocarcinoma (PDAC), gastric/gastroesophageal junction adenocarcinoma (G/GEJC), microsatellite stable colorectal cancer (MSS CRC), and squamous cell carcinoma of the head and neck (SCCHN).
  • Must have measurable disease by response evaluation criteria in solid tumors version 1.1 (RECIST v1.1).
  • Must have an Eastern Cooperative Oncology Group Performance Status of 0 or 1.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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Coordinator of this site? Confirm its status
DarlinghurstAustraliaUnknown status
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Elizabeth ValeAustraliaUnknown status
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MontrealCanadaUnknown status
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TorontoCanadaUnknown status
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Coordinator of this site? Confirm its status
Grand RapidsUnited StatesUnknown status
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Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status
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Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status
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Coordinator of this site? Confirm its status
Sioux FallsUnited StatesUnknown status
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Coordinator of this site? Confirm its status
TucsonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.