Cystic fibrosis drug Trikafta helps most but not all with the deadly genetic disease - The Boston Globe
Cystic fibrosis drug Trikafta helps most but not all with the deadly ge…
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Last month, the U.S. Food and Drug Administration approved the use of Trikafta® for children with cystic fibrosis ages 6 through 11 years old with certain mutations. This is an exciting milestone for many in the CF community, but especially for those with young children with CF who can now benefit from a modulator for the first time. You are an important part of this progress. Thank you for your continued support. | Cystic Fibrosis Foundation
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Last month, the U.S. Food and Drug Administration approved the use …
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CFTR modulators like Trikafta represent great progress in addressing the underlying cause of cystic fibrosis — but they do not cure the disease, and not everyone can benefit. Like Gina Ruiz, a 29-year-old living with CF who has two nonsense mutations. She shares her experience and some misconceptions about the disease. Learn more facts about CF: https://www.cff.org/intro-cf/dispelling-misconceptions-about-cystic-fibrosis | Cystic Fibrosis Foundation
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