The purpose of this study is to assess BMS-986500 as monotherapy in advanced solid tumors and as combination therapy in CDK4/6 inhibitor pre-treated advanced breast cancer.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
234
Specified dose of specified days
Specified dose on specified days
Specified dose on specified days
University of Alabama at Birmingham
Birmingham, Alabama, United States
Number of Participants With Dose Limiting Toxicities (DLTs)
Time frame: Up to Day 28 From Last Dose
Number of Participants With Adverse Events (AEs)
Time frame: Up to Day 28 From Last Dose
Number of Participants With Serious Adverse Events (SAEs)
Time frame: Up to Day 28 From Last Dose
Number of Participants With AEs Leading to Discontinuation
Time frame: Up to Day 28 From Last Dose
Number of Participants With TEAEs Leading to Death
Time frame: Up to Day 28 From Last Dose
Maximum Observed Serum Concentration (Cmax) of BMS-986500
Time frame: Up to Approximately 2 Years
Time of Maximum Observed Serum Concentration (Tmax) of BMS-986500
Time frame: Up to Approximately 2 Years
Area Under the Concentration-time Curve Within a Dosing Interval (AUC(TAU)) of BMS-986500
Time frame: Up to Approximately 2 Years
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com, www.BMSStudyConnect.com
CONTACT
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CONTACT
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