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NCT06764771RecruitingPhase 1

A Study of BMS-986488 as Monotherapy and Combination Therapy in Participants With Advanced Malignant Tumors

A Phase 1/1b Open-label Study of BMS-986488 as Monotherapy and Combination Therapy in Participants With Advanced Malignant Tumors

Source: ClinicalTrials.gov · Last updated 29 Jul 2026

Brief summary (registry, in English)

This purpose of this study is to determine if experimental treatment with BMS-986488, alone, or in combinations is safe, tolerable, and has anti-cancer activity in patients with advanced malignant tumors.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
437 (estimated)
First submitted
3 Jan 2025
Start date
25 Mar 2025
Primary completion date
15 Oct 2027
Lead sponsor
Bristol-Myers Squibb
NCT number
NCT06764771

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 437
  • From 25 Mar 2025 to the primary completion date, 15 Oct 2027
  • 8 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.

Prior treatment

  • History of prior severe cutaneous adverse reactions (SCARs), including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN).
    • \- Other protocol-defined inclusion/exclusion criteria apply.

Other illness

  • Impaired cardiac function or clinically significant cardiac disease.
  • For Parts 1B, 1C, 2B, 2C only (combination with adagrasib):.
    • History of pneumonitis or interstitial lung disease (ILD).

Other

  • Untreated central nervous system (CNS) metastases.
  • Leptomeningeal metastasis (carcinomatous meningitis).

Who the study is looking for

  • Participant must be ≥ 18 years of age.
  • Histologically confirmed diagnosis of a locally advanced and unresectable or metastatic solid tumor malignancy with any of the following tumor types:.
  • Part 1A: clear-cell renal cell carcinoma (ccRCC), clear-cell ovarian cancer (ccOC), non-small cell lung cancer (NSCLC), colorectal cancer (CRC), and pancreatic ductal adenocarcinoma (PDAC).
  • Parts 2A, 1D, 2D: ccRCC.
    • Part 1B: solid tumors with KRAS G12C mutation.
  • Part 2B: NSCLC with KRAS G12C mutation.
  • Parts 1C, 2C: colorectal cancer (CRC) with KRAS G12C mutation.
  • Participants must have an Eastern Cooperative Oncology Groups (ECOG) Performance Status of 0 or 1.
  • Participants must have measurable disease per RECIST v1.1.

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

Full criteria on ClinicalTrials.gov

Sites (8)

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

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
BrisbaneAustraliaActive, not recruiting
-
Coordinator of this site? Confirm its status
MontrealCanadaNot yet recruiting
Centre intégré de cancérologie du CHU de Québec Université Laval, Hôpital de l'Enfant-Jésus
Coordinator of this site? Confirm its status
QuébecCanadaRecruiting
BC Cancer - Vancouver
Coordinator of this site? Confirm its status
VancouverCanadaRecruiting
-
Coordinator of this site? Confirm its status
AllentownUnited StatesActive, not recruiting
-
Coordinator of this site? Confirm its status
DallasUnited StatesWithdrawn
The West Clinic, PLLC dba West Cancer Center
Coordinator of this site? Confirm its status
GermantownUnited StatesRecruiting
John Theurer Cancer Center at Hackensack University Medical Center
Coordinator of this site? Confirm its status
HackensackUnited StatesRecruiting

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