MHRA grants marketing authorization for Akeega
The UK’s Medicines and Healthcare products Regulatory agency (MHRA) has granted marketing authorization for Johnson & Johnson’s (NYSE: JNJ) Akeega (niraparib and abiraterone acetate dual-action pill), with prednisone or prednisolone, in combination with androgen deprivation therapy (ADT) for the treatment of adult patients with metastatic hormone-sensitive prostate cancer (mHSPC) and BRCA1/2 mutations (germline and/or somatic).
The US health care giant noted that the decision means the UK has licensed the first precision medicine combination for patients with BRCA1/2-mutated mHSPC, marking an important step towards more personalised care and potential future NHS access for eligible patients across the UK.
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