Akeega — abiraterone + niraparib
Named-patient access overview. Akeega is coordinated by Reserve Meds for international patients via physician-led cross-border sourcing.
About Akeega
Akeega (abiraterone + niraparib) is manufactured by Janssen Biotech (J&J) and indicated for mCRPC. It is a PARP + abi approved by the US FDA in 2023 and may be accessible to international patients through Named Patient Program or personal-import pathways.
How Reserve Meds coordinates Akeega
- Patient or treating physician submits a named-patient request.
- Clinical team verifies appropriateness of Akeega for the patient and destination country.
- Treating physician issues prescription and clinical justification.
- Country-specific NPP / personal-import documentation is prepared.
- Akeega is sourced from a DSCSA-compliant US specialty wholesaler with full serial traceability.
- Shipment is coordinated to the patient's physician or hospital pharmacy (cold-chain where required).
Access by country
We have documented named-patient access pathways for Akeega in the countries below. Each page outlines the destination-country regulatory posture, typical timeline, and physician-credential requirements.
Akeega in BahrainNamed-patient access, timeline, and regulatory notes
Akeega in BangladeshNamed-patient access, timeline, and regulatory notes
Akeega in JordanNamed-patient access, timeline, and regulatory notes
Akeega in KuwaitNamed-patient access, timeline, and regulatory notes
Akeega in NepalNamed-patient access, timeline, and regulatory notes
Akeega in PakistanNamed-patient access, timeline, and regulatory notes
Akeega in QatarNamed-patient access, timeline, and regulatory notes
Akeega in Sri LankaNamed-patient access, timeline, and regulatory notes
Start a request for Akeega
Submit a 60-second intake. Our clinical team responds within one business day with case-specific feasibility, timeline, and a formal quote.