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August 11, 2022

TORONTO, August 11, 2022 – New Brunswick has expanded access to the revolutionary cystic fibrosis (CF) drug, Trikafta, effective as of July 28, 2022. New Brunswick is the latest Canadian jurisdiction to fund the drug for children and adults aged six and older with at least one F508del gene mutation. Ontario, Alberta, Nova Scotia, Saskatchewan, Prince Edward Island, the Northwest Territories and the Non-Insured Health Benefits (NIHB) have also expanded access to Trikafta. In 2021, New Brunswick was one of four provinces that did not require eligible patients to meet a restrictive start criterion around lung function for the 12 and older age group to access the drug. Cystic Fibrosis Canada urges the remaining provinces and territories who have not yet followed CADTH's recent recommendation to provide Trikafta, to immediately fund Trikafta for all who can benefit.

Trikafta is considered the single greatest innovation in the history of cystic fibrosis. It can treat up to 90% of Canadians with cystic fibrosis and addresses the underlying causes of the disease instead of just managing the symptoms, potentially preventing irreversible damage caused by this progressive disease.

“This is a day that our community has fought long and hard for. Today’s news will change the trajectory of the disease, and the future, for many children in New Brunswick who live with cystic fibrosis,” said Dr. John Wallenburg, Chief Scientific Officer, Cystic Fibrosis Canada. “Now, we call on the remaining provinces and territories to move swiftly to cover this drug for those aged six and older and for other jurisdictions that have implemented restrictive start criterion, to fund the drug under CADTH’s new guidance.”

Health Canada approved Trikafta for use in the six to 11 age group in April 2022 and on July 6, 2022, CADTH issued a positive recommendation to fund the drug. This new recommendation from CADTH supersedes the recommendation issued in 2021 for the 12 and older age group, which included a recommendation to implement a restrictive start criterion of a lung function measurement of 90% or less.

Cystic Fibrosis Canada now calls on all other provinces and territories to follow the lead of New Brunswick, Saskatchewan, Nova Scotia, Alberta, Ontario, PEI, the Northwest Territories and NIHB and quickly fund Trikafta under their respective drug?programs using CADTH’s new recommendation and Cystic Fibrosis Canada’s clinician-developed guidelines for access and continuation. This drug should be accessible for all who could benefit from it.

“Children with cystic fibrosis between the ages of 6 and 11 will no longer have to wait and risk getting sicker to get access to a revolutionary drug. Trikafta will allow them to maintain good health. The future is now theirs! This is a great day for families living with cystic fibrosis in New Brunswick," said Maryse Haché, mother of a child with cystic fibrosis.

For CF advocacy news, subscribe to Cystic Fibrosis Canada’s advocacy e-newsletter?"The Advocacy Brief".

Members of the community and supporters are invited to join Cystic Fibrosis Canada’s #TrikaftaToday briefing on Wednesday, August 24 at 2pm ADT to discuss the most recent updates related to accessing Trikafta in Canada. Follow this link to register for the briefing.

About cystic fibrosis

Cystic fibrosis is the most common fatal genetic disease affecting 4,332 Canadian children and young adults. There is no cure. Of the Canadians with cystic fibrosis who died in the past five years, half were under the age of 37. Cystic fibrosis is a progressive, degenerative multi-system disease that affects mainly the lungs and digestive system. In the lungs, where the effects are most devastating, a build-up of thick mucus causes severe respiratory problems. Mucus and protein also build up in the digestive tract, making it difficult to digest and absorb nutrients from food. In addition to the physical effects of the disease, mental health concerns are emerging; anxiety and depression are common among this population. Double lung transplants are the final option for patients with end-stage disease; most fatalities of people with CF are due to lung disease.

About Cystic Fibrosis Canada

Cystic Fibrosis Canada has dramatically changed the cystic fibrosis story. We have advanced research and care that has more than doubled life expectancy. Since being founded by parents in 1960, Cystic Fibrosis Canada has grown into a leading organization with a central role engaging people living with cystic fibrosis, parents and caregivers, volunteers, researchers and healthcare professionals, government and donors. We work together to change lives for the 4,332 Canadian children and adults living with cystic fibrosis through treatments, research, information and support. Despite our remarkable progress together, we are not yet done. Not when half of the Canadians with cystic fibrosis who died in the past three years were under the age of 34. We will keep pushing, keep going further until all people with cystic fibrosis can and do experience everything life has to offer —and enjoy everything life has to offer. Learn more at


For more information:

Tel: (905)?317-5529


Nicole Young, Director, Marketing and Communications

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