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While it is disappointing that the PTAC only recommended a medium priority for Trikafta despite Pharmac’s Respiratory Advisory Committee giving it a high priority, the drug is on Pharmac’s Options for Investment list for both age groups and they are engaging in commercial negotiations with Vertex on a price.

In its Summary of Assessment, Pharmac states that it estimates Trikafta could give people with cystic fibrosis an additional 27 years of full health, improving not only the duration of their life, but also their quality of life. Pharmac also recognises that despite the high price tag of this treatment per person, “…funding Trikafta would reduce the spend on other medicines and other health sector costs, such as hospitalisations and lung transplants”, and they also appreciate that if Trikafta were funded, “this would make a significant financial difference to people with cystic fibrosis, their whānau and their communities”.

It is pleasing to see the transparency of the review process and decision-making from Pharmac, and in particular this step forward for Trikafta, however, there is still a way to go to see this drug and others for rare disorders funded and accessible to those who need them. Rare Disorders NZ looks forward to continue working with Pharmac on these issues to support improved health outcomes for those with rare disorders.

Trikafta is a treatment for the rare chronic condition cystic fibrosis, which currently affects around 500 New Zealanders.  

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Rare Disorders NZ is the collective voice of all people living with a rare disorder and their whānau. Our rare collective is made up of more than 150 disorder-specific support groups.

Our work is informed by the issues important to our collective. We work together to improve healthcare and wellbeing for everyone living with a rare health condition in New Zealand.

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