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Editorial
. 2024 Oct;59(10):2369-2371.
doi: 10.1002/ppul.27130. Epub 2024 Jun 13.

Adding fuel to the fire: The growing case for global access to cystic fibrosis transmembrane conductance regulator modulator therapy

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Editorial

Adding fuel to the fire: The growing case for global access to cystic fibrosis transmembrane conductance regulator modulator therapy

Brenda M Morrow et al. Pediatr Pulmonol. 2024 Oct.
No abstract available

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References

REFERENCES

    1. Wainwright CE, Elborn JS, Ramsey BW, et al. Lumacaftor–ivacaftor in patients with cystic fibrosis homozygous for Phe508del CFTR. N Engl J Med. 2015;373(3):220‐231. doi:10.1056/NEJMoa1409547
    1. Bell SC, Mall MA, Gutierrez H, et al. The future of cystic fibrosis care: a global perspective. Lancet Respir Med. 2020;8(1):65‐124. doi:10.1016/S2213-2600(19)30337-6
    1. Balfour‐Lynn IM, King JA. CFTR modulator therapies—effect on life expectancy in people with cystic fibrosis. Paediatr Respir Rev. 2022;42:3‐8. doi:10.1016/j.prrv.2020.05.002
    1. Gifford AH, Taylor‐Cousar JL, Davies JC, McNally P. Update on clinical outcomes of highly effective modulator therapy. Clin Chest Med. 2022;43(4):677‐695. doi:10.1016/j.ccm.2022.06.009
    1. McCoy KS, Blind J, Johnson T, et al. Clinical change 2 years from start of elexacaftor–tezacaftor–ivacaftor in severe cystic fibrosis. Pediatr Pulmonol. 2023;58(4):1178‐1184. doi:10.1002/ppul.26318

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