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A Randomized, Double-Blind, Multicenter Phase 3 Trial of BMS-986489 (BMS-986012 + Nivolumab Fixed Dose Combination) in Combination with Carboplatin plus Etoposide vs Atezolizumab in Combination with Carboplatin plus Etoposide as First-line Therapy in Extensive-Stage Small Cell Lung Cancer

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-515740-23-00
Acronym
CA245-0001
Enrollment
212
Registered
2025-03-10
Start date
2025-03-25
Completion date
Unknown
Last updated
2025-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Extensive-Stage Small Cell Lung Cancer (ES-SCLC)

Brief summary

Overall survival: how long participants live after entering the study (i.e. after randomization)

Detailed description

Time for disease related symptoms to get worse (TTDD)., Safety: side effects, the number of side effects, type, severity, seriousness, and outcome., Response: measurements to indicate how many patients' tumors shrink or disappear after treatment (Overall Response)., How long the tumors stay shrunk or disappear (Duration of Response), The time during and after treatment that a participant lives without their disease getting worse (Progression Free Survival).

Interventions

DRUGETOPOSIDE
DRUGATEZOLIZUMAB
DRUGAtigotatug + Nivolumab FDC
DRUGCARBOPLATIN

Sponsors

Bristol-Myers Squibb Services Unlimited Company
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Overall survival: how long participants live after entering the study (i.e. after randomization)

Secondary

MeasureTime frame
Time for disease related symptoms to get worse (TTDD)., Safety: side effects, the number of side effects, type, severity, seriousness, and outcome., Response: measurements to indicate how many patients' tumors shrink or disappear after treatment (Overall Response)., How long the tumors stay shrunk or disappear (Duration of Response), The time during and after treatment that a participant lives without their disease getting worse (Progression Free Survival).

Countries

Austria, Belgium, Czechia, France, Germany, Greece, Italy, Netherlands, Poland, Romania, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026