New Zealand’s Pharmaceutical Management Agency PHARMAC had approved an agreement with Merck Sharpe and Dohme (MSD), the local subsidiary of US pharma giant Merck & Co (NYSE: MRK) for the funding of pembrolizumab (Keytruda), posaconazole (Noxafil) and raltegravir (Isentress) and decisions to amend the Special Authority criteria applying to nivolumab and establish a “programmed cell death-1 (PD-1) inhibitors” therapeutic sub-group from September 2016.
This was the subject of a consultation in June. No changes were made to the proposal following consultation.
In summary, the effect of the decisions is that from September 2016:
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