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A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of BMS-986489 in Chinese Participants With Relapsed/Refractory Small Cell Lung Cancer

StatusCompleted
PhasePhase 1
Started2025-05-07
View on ClinicalTrials.gov ↗

Amendment history

2026-09-25
notable
Trial completed
Primary completion confirmed: September 2026 (last estimated May 2027)
2026-05-11
minor
Study Status, Outcome Measures, IPDSharing v4
Secondary endpointsdetails revised at 7 of 7 entries
2025-08-25
notable
Recruiting→Active, Not Recruiting Study Status, Contacts/Locations v3
Trial statusRecruiting→Active, Not Recruiting
Study sites5 entries, revised
ShandongLocal CancerInstitution Hospital- 0003 LinYiLocal CancerInstitution Hospital- 0001 SirLocal RunInstitution Run- Shaw0005 Local HospitalInstitution of- Zhejiang University School of Medicine Shanghai East Hospital0002
2025-06-05
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2025-07-31→confirmed 2025-05-07
Study sites5 entries, revised
LocalShandong InstitutionCancer -Hospital LinYi 0003Cancer Hospital LocalSir InstitutionRun -Run 0001Shaw Hospital of Zhejiang University School of Medicine LocalShanghai InstitutionEast - 0005 Local Institution - 0002Hospital
2025-03-20
minor
Study Status, Contacts/Locations, References v1
Study sites1→5
2025-01-24
minor
Original filing
The purpose of this study is to characterize the safety, tolerability, pharmacokinetics, and preliminary efficacy of BMS-986489 in Chinese participants with R/R SCLC (Relapsed/Refractory Small Cell Lung Cancer).
Trial Details
NCT Number NCT06799286
Lead Sponsor Bristol-Myers Squibb
Conditions Small Cell Lung Carcinoma
Enrollment 10 participants
Start Date 2025-05-07
Primary Completion 2026-09-09 (estimated)
Study Completion 2026-09-09 (estimated)
Updated on ClinicalTrials.gov 2026-09-24