A Study of BMS986365 in Combination with Degarelix before Radical Prostatectomy for Treating People with High-Risk Localized Prostate Cancer

Inclusion Criteria

• Participant or participant’s legally authorized representative (LAR) is willing and able to provide written informed consent and privacy authorization for the release of personal health information. A signed informed consent must be obtained before screening procedures are performed
• Individuals with prostate cancer 18 years of age and above
• Histological or cytological evidence of prostate cancer
• Documented high-risk localized prostate cancer based on one or more of the following National Comprehensive Cancer Network (NCCN) criteria: * Prostate specific antigen (PSA) >= 20ng/ml or * Gleason >= 8 or * Clinical stage >= cT3a
• Candidate for RP as determined by treating physician
• Eastern Cooperative Oncology Group (ECOG) performance status =< 2
• Absolute neutrophil count (ANC) >= 1.5 K/mcL (within 28 days of registration)
• Hemoglobin >= 9g/dL (within 28 days of registration)
• Platelet count >= 100 K/mcL (within 28 days of registration)
• Potassium within institutional normal range (within 28 days of registration) * If these electrolytes are corrected with supplements, eligibility should be confirmed prior to the first dose of study intervention
• Calcium within institutional normal range (within 28 days of registration) * If these electrolytes are corrected with supplements, eligibility should be confirmed prior to the first dose of study intervention
• Magnesium within institutional normal range (within 28 days of registration) * If these electrolytes are corrected with supplements, eligibility should be confirmed prior to the first dose of study intervention
• Total bilirubin =< 1.5 x upper limit of normal (ULN) (Note: In participants with Gilbert's syndrome, if total bilirubin is > 1.5 x ULN, measure direct and indirect bilirubin and if direct bilirubin is =< 1.5 x ULN, participant may be eligible) (within 28 days of registration)
• Serum glutamic-oxaloacetic transaminase (SGOT) (aspartate aminotransferase [AST]) =< 2.5 x ULN (within 28 days of registration)
• Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase [ALT]) =< 2.5 x ULN (within 28 days of registration)
• Creatinine clearance (CrCl) > 60 mL/min (within 28 days of registration) * Using Cockcroft-Gault equation or measured CrCl using 24-hour urine collection
• Male participants: * A participant who is sexually active with individuals of childbearing potential (IOCBP) must agree to follow instructions for method(s) of contraception as described below and included in the informed consent form ** Note: Azoospermic males are not exempt from contraceptive requirements and will be required to always use a latex or other synthetic condom during any sexual activity (e.g., vaginal, anal, oral) with IOCBP, even if the participant has undergone a successful vasectomy or if the partner is pregnant * Participants will be required to always use a latex or other synthetic condom during any sexual activity (e.g., vaginal, anal, oral) with IOCBP, even if the participant has undergone a successful vasectomy or if the partner is pregnant or breastfeeding. Male (as assigned at birth) participants should continue to use a condom during the intervention period and for at least 2 months (for BMS-986365) and as per the label for degarelix after the last dose of study intervention * IOCBP partners of participants should be advised to use a highly effective method of contraception during the intervention period and for at least 2 months (for BMS-986365) and as per the label for degarelix after the last dose of study intervention for the male participant * Participants with a pregnant or breastfeeding partner must agree to remain abstinent from sexual activity or use a male condom during any sexual activity (eg, vaginal, anal, oral), even if the participant has undergone a successful vasectomy, during the intervention period and for at least 2 months (for BMS-986365) and as per the label for degarelix after the last dose of study intervention * Participants must refrain from donating sperm during the intervention period and for at least 2 months (for BMS-986365) and as per the label for degarelix after the last dose of study intervention * Breastfeeding partners of participants should be advised to consult their health care provider about using appropriate highly effective contraception during the time the male participant is required to use condoms

Exclusion Criteria

• Radiographic evidence of distant (extra-pelvic) metastatic prostate cancer on CT and/or MRI, bone scan or PET scan (any PET modality) * Patients with N1 disease may be eligible for the study if planned for a radical prostatectomy per standard-of-care/institutional guidelines
• On androgen deprivation therapy (ADT) (gonadotrophin releasing hormone [GnRH] agonists or antagonists) for > 4 weeks at time of consent
• Other than ADT, prior systemic therapy for treatment of their prostate cancer, including but not limited to chemotherapy, immunotherapy, etc
• Prior local therapy to the prostate for prostate cancer, including but not limited to radiation, high-intensity focused ultrasound (HIFU), phototherapy, etc
• Participants who are considered a poor medical risk due to a serious, uncontrolled medical disorder, or recovering from a recent surgery (approximately within 1 month, or as deemed recent per surgeon), for which in the opinion of the investigator would interfere with treatment on this study
• Any patient who cannot swallow oral medications or have gastrointestinal disorders in the opinion of the investigator are likely to interfere with absorption
• Participant has impaired cardiac function or clinically significant cardiac disease, including any of the following: * Left ventricular ejection fraction (LVEF) < 50% as determined by ECHO or MUGA scan at screening * Complete left bundle branch, high-grade atrioventricular (AV) block (eg, bifascicular block, Mobitz type II and third-degree AV block), or other clinically significant abnormal electrocardiogram (ECG) finding at screening. Participant with a permanent pacemaker are excluded * History of clinically significant sinus bradycardia or sick sinus syndrome or bradycardia with heart rate < 50 beats per minute (bpm) at screening. (Note: All is determined by the average of the triplicate screening ECG, based on local reading.) ** A prolongation of the QT interval on screening ECG as defined by repeated demonstration of a corrected QT (QTc) interval >= 450 ms using Fridericia’s formula-corrected QT (QTcF) ** Participant would be excluded if the QTcF interval cannot be determined on the screening ECG (eg, unreadable or not interpretable) ** In the presence of right bundle branch block, if measured QTcF is > 450 ms at baseline, then the ECG for QTc reading should be verified by a cardiologist to confirm eligibility * A history of sustained ventricular tachycardia, ventricular fibrillation, Torsades de Pointes (TdP), or resuscitated cardiac arrest, individual or family history of long QT syndrome, or cardiomyopathy * Concurrent treatment with antiarrhythmic or other drugs that prolong the QT interval. For study eligibility, a washout period of >= 5 half-lives must have elapsed prior to the first dose of study intervention. * Congestive heart failure (New York Heart Association class III or IV) =< 12 months prior to the first dose of study intervention * Myocardial infarction, myocarditis, or pericarditis =< 6 months prior to the first dose of study intervention * Unstable or poorly controlled angina pectoris (including the Prinzmetal variant of angina pectoris) or symptomatic peripheral vascular disease * Poorly controlled hypertension (systolic blood pressure [BP] >= 160 mmHg or diastolic BP >= 95 mmHg). Participants with a history of hypertension can be enrolled if the investigator considers that BP is controlled by antihypertensive treatment
• Participants with clinically significant venous thromboembolism (eg, pulmonary embolism and deep vein thrombosis) within 3 months prior to the first dose of study intervention
• Active viral hepatitis, including the following: * Any positive test result for hepatitis B virus (HBV) indicating presence of virus, eg, HBV DNA positive would be excluded. Participants with hepatitis B virus surface antibody (anti-HBs) positive in line with prior vaccination are eligible to enroll * Any positive test result for hepatitis C virus (HCV) indicating presence of active viral replication (detectable HCV-RNA) * Participants with positive HCV antibody and an undetectable HCV RNA are eligible to enroll
• Known HIV positive with an AIDS defining opportunistic infection within the last year, or a current CD4 count < 350 cells/uL. Participants with HIV are eligible if: * Participant has received antiretroviral therapy (ART) for at least 4 weeks prior to treatment assignment as clinically indicated while enrolled on study and an HIV viral load less than 400 copies/mL prior to enrollment * Participant continues on ART as clinically indicated while enrolled on study * In the case ART is at risk of drug-drug interaction, participants should be switched to an alternate effective ART regimen (with minimal drug-drug interaction potential) before study participation or should be excluded from the study if their regimen cannot be altered * CD4 counts and viral load are monitored per standard of care by a local health care provider
• Any other active malignancy at time of first dose of study treatment or diagnosis of another malignancy within 3 years prior to first dose of study treatment that requires active treatment, except for basal or squamous cell skin cancer or superficial bladder cancer that has previously been treated
• Use of any prohibited concomitant medications including herbal supplements within 2 weeks prior to treatment start
• Receiving any other investigational agents within 4 weeks or 5x the half-life of investigational agent (whichever is longer) from this study’s treatment start
• Known allergy to any of the compounds under investigation
• Any other condition which, in the opinion of the investigator, would preclude participation in this trial