Pharmac says it's seeking expert clinical advice on whether to fund a Opdivo.
The agency confirms the medicine's manufacturer, Bristol-Myers Squibb, has made an application for the medicine to be state-funded for advanced melanoma and advanced squamous and non-squamous non-small-cell lung cancers.
Keytruda and Opdivo both gained "breakthrough therapy" status from the United States Food and Drug Administration.
They are in the class called PD-1 inhibitors. They block the PD-1 receptor protein on certain immune system cells, which allows them to detect and destroy the cancer cells.
The registration of Opdivo in New Zealand opens the possibility of Pharmac trying to bargain prices down between Opdivo and Keytruda or negotiate discounts.
Opdivo is approved in New Zealand:
• as a stand-alone treatment to treat patients with advanced melanoma
• in combination with Yervoy (ipilimumab), another BMS drug, to treat patients with advanced melanoma
• to treat patients with advanced squamous non-small cell lung cancer (NSCLC) who have progressed on or following prior chemotherapy
• to treat patients with advanced non-squamous non-small cell lung cancer who have progressed on or following prior therapy.