Health Canada has issued marketing authorisation to Vertex Pharmaceuticals for the expanded use of the company’s Trikafta (elexacaftor/tezacaftor/ivacaftor and ivacaftor) to include children with cystic fibrosis (CF) of the age six to 11 years.

The treatment is indicated for these CF patients with a minimum of one F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. 

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

An oral tablet, Trikafta is created to boost CFTR protein’s quantity and function at the cell surface.

With the authorisation, nearly 500 Canadians with CF of this age group will be eligible to receive Trikafta.

Furthermore, an additional dosage strength of Trikafta tablets will be offered in the country (elexacaftor 50mg/tezacaftor 25mg/ivacaftor 37.5mg and ivacaftor 75mg).

In a 24-week, open-label, multicentre Phase III trial in CF patients aged six to 11 years, Trikafta was found to be well tolerated.

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData

In addition, safety data from the trial was in line with prior data from subjects aged 12 years and above.

The trial analysing the safety, pharmacokinetics and efficacy of Trikafta enrolled a total of 66 CF patients with either two copies of the F508del mutation or a copy of the F508del mutation and one minimal function mutation.

The latest indication was submitted by the company to the Canadian Agency for Drugs and Technologies in Health (CADTH) and the Institut national d’excellence en santé et en services sociaux (INESSS) in Québec for Health Technology Assessments.

Vertex Pharmaceuticals CEO and president Reshma Kewalramani said: “We are delighted that Trikafta is now available for these young patients in Canada. 

“It provides a new treatment option for those with CF ages 6-11 years with at least one F508del mutation and a first-in-class treatment option for the approximately 500 6-11-year-olds who are newly eligible for a medicine that treats the underlying cause of their disease.

In January this year, the European Commission granted approval for label extension of the combination regimen of Vertex Pharmaceuticals’ Kaftrio (ivacaftor/tezacaftor/elexacaftor) with ivacaftor to treat CF in children of the age six to 11 years.

This content was updated on 25 January 2024

Pharmaceutical Technology Excellence Awards - Nominations Closed

Nominations are now closed for the Pharmaceutical Technology Excellence Awards. A big thanks to all the organisations that entered – your response has been outstanding, showcasing exceptional innovation, leadership, and impact.

Excellence in Action
NorthWest EHealth has won three 2025 Pharmaceutical Technology Excellence Awards for Innovation, Safety and Diversity. Explore how its ConneXon platform is transforming SAE reporting and real-time safety oversight, while FARSITE delivers socio-economically inclusive recruitment to boost trial efficiency, data integrity and regulatory-grade representativeness.

Discover the Impact