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BMS-986490

Phase 1

Advanced Solid Tumors | Small molecule | Oncology |Bristol-Myers Squibb Company|Last Updated: Sep 1, 2026

Success Probability

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Market & Valuation

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Trial Design

RandomizedCONTROLLED
Total Trials1
Total Enrollment360

FDA Designations

No designations recorded

Clinical trial landscape

BMS-986490 · 1 trial · 1 indication

Phase 1 1
NCT06730750A Study of BMS-986490 With or Without Bevacizumab in Advanced Solid TumorsAdvanced Solid Tumors
ACTIVE NOT_RECRUITING360 Analytics
PHASE1ACTIVE NOT_RECRUITING
A Study of BMS-986490 With or Without Bevacizumab in Advanced Solid Tumors
Advanced Solid TumorsUnlock trial analytics

Study Endpoints

Primary Endpoints

Number of participnats with Adverse Events (AEs)
Up to 100 days following discontinuation of dosing
Number of participants with Serious AEs (SAEs)
Up to 100 days following discontinuation of dosing
Number of participants with AEs meeting protocol-defined dose limiting toxicity (DLT) criteria
Up to 28 days after the first treatment of study intervention
Number of participants with AEs leading to discontinuation
Up to 100 days following discontinuation of dosing
Number of deaths
Up to 100 days following discontinuation of dosing

Secondary Endpoints

Area under the concentration-time curve in 1 dosing interval (AUC(TAU))
Approximately 30 Days after Cycle 30, Day 1 (1 Cycle = 21 Days)
Trough observed concentration (Ctrough)
Approximately 30 Days after Cycle 30, Day 1 (1 Cycle = 21 Days)
Maximum observed concentration (Cmax)
Approximately 30 Days after Cycle 30, Day 1 (1 Cycle = 21 Days)
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Study Design & Arms

AllocationRANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Part 1AEXPERIMENTAL -
Part 2A - Colorectal Cancer (CRC)EXPERIMENTAL -
Part 2A - Non-Small Cell Lung Cancer/Gastric Cancer (NSCLC/GC)EXPERIMENTAL -
Part 1BEXPERIMENTAL -
Part 2BEXPERIMENTAL -

Interventions

NameTypeDescription
BMS-986490DRUGSpecified dose on specified days.
BevacizumabDRUGSpecified dose on specified days.
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites6

Inclusion Criteria: * Documented histologically or cytologically confirmed, advanced, unresectable/metastatic solid tumor measurable by RECIST v1.1. * CRC: Part 1A, Part 2A-CRC, Part 1B, and Part 2B: i) Locally advanced/metastatic, recurrent, or unresectable CRC with adenocarcinoma histology and...

Countries:United StatesAustraliaCanada
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Competitive Landscape -Other Solid Tumors 9 trials (matched to "Advanced Solid Tumors")

Recent Changes (Last 90 Days)

MEDIUMSep 1, 2026NCT06730750Status: RECRUITING → ACTIVE_NOT_RECRUITING
MEDIUMSep 1, 2026NCT06730750Status: RECRUITING → ACTIVE_NOT_RECRUITING
LOWJul 2, 2026NCT06730750lastUpdatePostDate: changed
LOWJul 2, 2026NCT06730750lastUpdatePostDate: changed

Frequently asked questions about BMS-986490

What is BMS-986490 used for?

BMS-986490 is an investigational small molecule being developed for the treatment of advanced solid tumors. It is currently in Phase 1 clinical development and is not yet approved by regulatory authorities.

Who makes BMS-986490?

BMS-986490 is being developed by Bristol-Myers Squibb Company, a biopharmaceutical company listed on the New York Stock Exchange under the ticker symbol BMY.

What phase is BMS-986490 in?

BMS-986490 is in Phase 1 clinical development. It is an investigational drug and has not been approved by the FDA or other regulatory agencies. The drug is being studied in patients with advanced solid tumors.

What clinical trials is BMS-986490 in?

BMS-986490 is being studied in a Phase 1 clinical trial with the identifier NCT06730750. This trial evaluates BMS-986490 with or without bevacizumab in patients with advanced solid tumors and is enrolling approximately 360 participants in the United States, Australia, and Canada.

Is BMS-986490 being studied in a randomized trial?

Yes, the Phase 1 clinical trial of BMS-986490 (NCT06730750) is randomized and controlled. The trial is not double-blinded, and it is currently active but not recruiting participants.