A Study to Learn More About How Safe Darolutamide is and How Well it Works Under Real World Conditions When Taken in Addition to Standard Androgen Deprivation Therapy (ADT) in Indian Participants With High-risk Non-metastatic Castration-resistant Prostate Cancer (nmCRPC)

Launched by BAYER · Apr 21, 2022

Keywords

ClinConnect Summary

This clinical trial is studying the safety and effectiveness of a medication called darolutamide when used together with standard hormone therapy (called androgen deprivation therapy, or ADT) in men with high-risk non-metastatic castration-resistant prostate cancer. This type of cancer hasn’t spread to other parts of the body but continues to grow despite low levels of male hormones. The researchers want to see how well darolutamide works in Indian patients, as previous studies did not include participants from India.

To be eligible for this trial, participants must be men aged 18 years or older who have been diagnosed with prostate cancer that is resistant to hormone treatment but has not spread. They should also have specific levels of a substance called PSA in their blood, which helps indicate cancer progression. Throughout the study, participants will take darolutamide as a pill twice a day and will visit the study center every 16 weeks for check-ups. During these visits, their health will be monitored through blood tests, physical exams, and questionnaires about their well-being. If the trial is stopped, participants may still have the chance to continue receiving darolutamide if they are benefiting from it.

Gender

MALE

Eligibility criteria

• Inclusion Criteria:
• • Capable of giving signed informed consent.
• • Participant must be male aged ≥ 18 years.
• • Histologically or cytologically confirmed adenocarcinoma of prostate without neuroendocrine differentiation or small cell features.
• * Castration resistance, demonstrated by:
• • a minimum of 3 rising PSA values while the participant is on continuous ADT (started at least 4 weeks prior to the PSA measurement or, PSA measured at least 4 weeks after bilateral orchiectomy) and
• • the interval between each PSA measurement must be ≥ 1 week, and
• • the PSA value at screening must be ≥ 1.0 ng/mL (1.0 μg/L). To confirm this eligibility criterion, it is acceptable for 2 out of the 3 PSA measurements to be taken during the 28-day screening period (after participant has signed consent), provided the measurements are ≥ 1 week apart. In this case, the last PSA value should be recorded as the screening value.
• • Castrate level of serum testosterone (\< 1.7 nmol/L \[50 ng/dL\]) on gonadotropin releasing hormone (GnRH) agonist or antagonist therapy or after bilateral orchiectomy. Participants who have not undergone bilateral orchiectomy must continue GnRH therapy during the study.
• • PSA doubling time (PSADT) of ≤ 10 months.
• • Eastern cooperative oncology group (ECOG) performance status (PS) of 0 or 1.
• • Estimated glomerular filtration rate (eGFR) \> 15 mL/min/1.73 m\^2.
• • Blood counts at screening: hemoglobin ≥ 9.0 g/dL, absolute neutrophil count ≥ 1500/μL (1.5 × 109/L), platelet count ≥ 100,000/μL (100 ×109/L) (participant must not have received any growth factor or blood transfusion within 7 days of the hematology laboratory obtained at screening).
• • Screening values of serum alanine aminotransferase (ALT) and aspartate transaminase (AST) ≤ 2.5 × upper limit of normal (ULN), total bilirubin (TBL) ≤ 1.5 × ULN (except participants with a diagnosis of Gilbert's disease), creatinine ≤ 2.0 × ULN.
• • Sexually active participants, unless surgically sterile, must agree to use a male condom plus partner use of a contraceptive method with a failure rate of \<1% per year, and refrain from sperm donation during the study treatment and for 1 week after the last dose of study treatment. Contraceptive use by men should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
• Exclusion Criteria:
• • History of metastatic disease at any time or presence of detectable metastases by investigator assessment within 42 days prior to start of study treatment based on standard medical imaging, i.e., computed tomography/ magnetic resonance imaging (CT/MRI) and bone scan. (Lesions seen on prostate-specific membrane antigen /positron emission tomography (PSMA/PET) scan that are not detected on standard imaging do not exclude participation.) Presence of pelvic lymph nodes \< 1.5 cm in short axis below the aortic bifurcation is allowed.
• • Symptomatic local-regional disease that requires medical intervention including moderate/severe urinary obstruction or hydronephrosis due to prostate cancer.
• • Acute toxicities of prior treatments and procedures not resolved to common terminology criteria for adverse events (CTCAE) v.5.0 grade ≤ 1 or baseline before first dose of study treatment.
• • Severe or uncontrolled concurrent disease, infection, or co-morbidity that, in the opinion of the investigator, would make the participant inappropriate for enrollment.
• • Known hypersensitivity to the study treatment or any of its ingredients.
• • Major surgery within 28 days before first dose of study treatment.
• • Any of the following within 6 months before first dose of study treatment: stroke, myocardial infarction, severe/unstable angina pectoris, coronary/peripheral artery bypass graft; congestive heart failure New York Heart Association Class III or IV.
• • Uncontrolled hypertension as indicated by a systolic blood pressure (BP) ≥ 160 mmHg or diastolic BP ≥ 100 mmHg at screening despite medical management. Participants with hypertension can enroll provided BP is stable and controlled by anti-hypertensive treatment.
• • End-stage renal disease (eGFR \< 15 mL/min/1.73 m\^2).
• • Prior malignancy. Adequately treated basal cell or squamous cell carcinoma of skin or superficial bladder cancer that has not spread behind the connective tissue layer (i.e., pTis, pTa, and pT1) is allowed, as well as any other cancer for which treatment has been completed ≥ 5 years ago and from which the participant has been disease-free.
• • Gastrointestinal disorder or procedure which expects to interfere significantly with absorption of study treatment.
• • Unstable active viral hepatitis with a need for treatment.
• * Known human immunodeficiency virus (HIV) infection with any of the following (Note: HIV testing is not required unless mandated by local authority):
• • CD4+ T-cell (CD4+) count of less than 350 cells/μL
• • History of acquired immunodeficiency syndrome (AIDS)-defining opportunistic infection within the past 12 months
• • On established antiretroviral therapy for less than 4 weeks
• • Presenting with a viral load of more than 400 copies/mL prior to enrollment
• • On antiretroviral therapy or prophylactic antimicrobials that are expected to cause significant drug-drug interactions or overlapping toxicities with study treatment and cannot be changed to alternative agents.
• • Any condition that, in the opinion of the investigator, would impair the participants' ability to comply with the study procedures or study treatment (e.g., unable to swallow study treatment).
• • Unwilling or unable to comply with all protocol-required visits and assessments or comply with study requirements.
• * Prior treatment with:
• • Second-generation androgen receptor (AR) inhibitors (such as enzalutamide, apalutamide, darolutamide, proxalutamide, etc)
• • Other investigational AR inhibitors
• • Cytochrome P450 (CYP17) enzyme inhibitors (such as oral ketoconazole, abiraterone acetate, TAK-700, etc).
• • Use of first-generation AR inhibitors (bicalutamide, flutamide, nilutamide, cyproterone acetate) within 28 days before first dose of study treatment.
• • Use of estrogens or 5-α reductase inhibitors (finasteride, dutasteride) within 28 days before first dose of study treatment.
• • Prior chemotherapy or immunotherapy for prostate cancer, except adjuvant/neoadjuvant treatment completed \> 2 years before first dose of study treatment.
• • Use of systemic corticosteroid with dose greater than the equivalent 10 mg of prednisone/day within 28 days before first dose of study treatment.
• • Radiation therapy (external beam radiation therapy, brachytherapy, or radiopharmaceuticals) within 12 weeks before first dose of study treatment.
• • Treatment with an osteoclast-targeted therapy (bisphosphonate or denosumab) to prevent skeletal-related events within 4 weeks before first dose of study treatment. Participants receiving osteoclast-targeted therapy to prevent bone loss at a dose and schedule indicated for osteoporosis may continue treatment at the same dose and schedule.
• • Treatment with any investigational drug within 28 days before first dose of study treatment.