Race Impact on Efficacy of Niraparib Plus Abiraterone Acetate and Prednisone in Patients With Homologous Repair Deficient Castration-resistant Prostate Cancer

Trial Title: Race Impact on Efficacy of Niraparib Plus Abiraterone Acetate and Prednisone in Patients With Homologous Repair Deficient Castration-resistant Prostate Cancer

NCT ID: NCT06527690

Condition: Prostate Cancer
Castrate Resistant Prostate Cancer
Homologous Recombination Deficiency

Conditions: Official terms:
Prostatic Neoplasms
Prednisone
Niraparib

Study type: Interventional

Study phase: Phase 2

Overall status: Not yet recruiting

Study design:

Allocation: Non-Randomized

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Niraparib/Abirate rone acetate fixed-dose combination
Description: Participants will receive niraparib/abiraterone acetate fixed-dose combination 100/500 mg 2 tablets once daily on days 1-28 of each 28-day cycle.
Arm group label: Racially self-identified as Native Indigenous American or self-identified Latino and racially White
Arm group label: self-identified as from Black racial origin irrespective of ethnicity

Intervention type: Drug
Intervention name: Prednisone
Description: Participants will receive prednisone 5mg 2 tablets once daily on days 1-28 of each 28-day cycle.
Arm group label: Racially self-identified as Native Indigenous American or self-identified Latino and racially White
Arm group label: self-identified as from Black racial origin irrespective of ethnicity

Summary: This is an open-label, multicenter, interventional study in racially self-identified black or ethnically self-identified hispanic and racially self-identified white or native American participants with metastatic castration-resistant prostate cancer whose tumors demonstrate molecular alterations compatible with homologous repair deficiency.

Detailed description: This study will enroll up to 70 participants, divided into two cohorts of 35 each. Cohort A will include participants self-identified as of black origin, as defined by the FDA Guidance on Collection of Race and Ethnicity Data in Clinical Trials, including those with more than one race, such as pardos. Cohort B will include (1) participants self-identified from Native Indigenous American origins and (2) participants self-identified from White origin who ethnically identify as Latinos, both as per the FDA guidance. The study will consist of five phases: Prescreening for biomarker evaluation, Screening, Treatment, Extension, and Follow-Up. Participants will be assessed during prescreening using the sponsor's required assays or previous results from CLIA-certified labs showing a pathogenic germline or somatic HRR alteration. The combination of niraparib/AA plus prednisone is FDA-approved for treating homologous repair deficient metastatic castration-resistant prostate cancer (HRD mCRPC). Given the benefits of this combination and the lack of representation in previous studies, a placebo-controlled study is deemed unethical. Thus, the study design includes two independent cohorts, both receiving the standard of care treatment. This study aims to provide additional information on the benefits of this therapy in underrepresented populations. Conducted with input from experts in racial inequities, the study results may be shared with participants through a plain language summary. Participants will be fully informed about the study's risks and requirements and will receive new information affecting their participation decision. Consent to participate is voluntary and can be withdrawn at any time without penalty. Written consent will be obtained following regulations and participant preferences.

Criteria for eligibility:
Criteria:
Eligibility criteria - Prescreening Inclusion Age: ≥18 years of age (or the local legal age of consent) Participant Origin: Participants of the following origins: - COHORT A: Participants self-identified as with black origin as defined as having origins in any of the black racial groups of Africa, as per the FDA Guidance on Collection of Race and Ethnicity Data in Clinical Trials, and irrespective of ethnicity. This includes participants with more than one race, including pardos. - COHORT B: Participants self-identified from Native Indigenous American origins as per the FDA Guidance on Collection of Race and Ethnicity Data in Clinical Trials, irrespective of ethnicity. This includes participants with more than one race, including mestizos. OR - Participants self-identified from White origin as per the FDA Guidance on Collection of Race and Ethnicity Data in Clinical Trials, and ethnically self-identified as Latinos. Participant and Disease Characteristics - ECOG Performance Status 0-1 - Histologically or cytologically confirmed metastatic prostate adenocarcinoma - Metastatic disease documented by conventional imaging with CT or MRI (for soft tissue lesions) or 99mTc bone scan (for bone lesions) 1. Participants with a single bone lesion on 99mTc bone scan with no other non-nodal metastatic disease must have confirmation of bone metastasis by CT or MRI. 2. Participants with lymph node-only disease are not eligible. - Willing to provide tumor tissue (archival) for determination of deleterious germline or somatic HRR gene alterations, if no local (testing done at investigator center or commercial testing) or prior sponsor-approved test result is available. 1.Testing must demonstrate pathogenic gene alterations in ≥1 of the following genes to proceed to screening: ATM, BRCA1, BRCA2, BRIP1, CDK12, CHEK2, FANCA, HDAC2, or PALB2. - Castration-resistant disease, defined by the PCWG3 as any of the following criteria while on castrate levels of testosterone (less than or equal to 50 ng/dL): 1. Visceral Progression OR 2. Bone progression (2 or more new prostate-cancer related new lesions compared to baseline) OR 3. PSA Progression, as defined by an increase in two consecutive measurements that fulfills all the following criteria: 1. The evaluations were performed with a minimum interval of 1 week. 2. Progressive worsening with an increase of at least 50% compared to baseline. 3. The minimum value of PSA is ≥ 1 ng/ml.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Start date: November 29, 2024

Completion date: February 28, 2029

Lead sponsor:
Agency: Latin American Cooperative Oncology Group
Agency class: Other

Collaborator:
Agency: Janssen, LP
Agency class: Industry

Source: Latin American Cooperative Oncology Group

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06527690