Regulatory approvals
ind:hc:akeega:0
Regulatory approval
Published by the Health Canada .
Approved
AKEEGA (niraparib and abiraterone acetate) is indicated with prednisone or prednisolone for the treatment of adult patients with deleterious or suspected deleterious BRCA mutated (germline and/or somatic) metastatic castration resistant prostate cancer (mCRPC), who are asymptomatic/mildly symptomatic, and in whom chemotherapy is not clinically indicated.
This is written in the approval
document .
Citation
Janssen Inc. Akeega (abiraterone acetate and niraparib) [product monograph]. Health Canada website. https://pdf.hres.ca/dpd_pm/00078864.PDF. Revised March 2025. Accessed June 2025.
Therapeutic response
Precision oncology relationships for therapeutic response derived from this regulatory approval.
Organizations
1 organization
Cancer types
1 cancer type
Organizations
Biomarkers
Cancer types
Therapies
HC (1)
BRCA1 oncogenic variants
Prostate Adenocarcinoma
Abiraterone acetate ,
Niraparib ,
Prednisone
HC (1)
BRCA1 pathogenic variants
Prostate Adenocarcinoma
Abiraterone acetate ,
Niraparib ,
Prednisone
HC (1)
BRCA2 oncogenic variants
Prostate Adenocarcinoma
Abiraterone acetate ,
Niraparib ,
Prednisone
HC (1)
BRCA2 pathogenic variants
Prostate Adenocarcinoma
Abiraterone acetate ,
Niraparib ,
Prednisone
HC (1)
BRCA1 oncogenic variants
Prostate Adenocarcinoma
Abiraterone acetate ,
Niraparib ,
Prednisolone
HC (1)
BRCA2 oncogenic variants
Prostate Adenocarcinoma
Abiraterone acetate ,
Niraparib ,
Prednisolone
HC (1)
BRCA1 pathogenic variants
Prostate Adenocarcinoma
Abiraterone acetate ,
Niraparib ,
Prednisolone
HC (1)
BRCA2 pathogenic variants
Prostate Adenocarcinoma
Abiraterone acetate ,
Niraparib ,
Prednisolone
Contributions
Date
Contributor
Description
2024-10-30
Van Allen lab
Initial access of FDA approvals