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Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes

Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2607578582

Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes

About this item

Full title

Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes

Publisher

United States: Massachusetts Medical Society

Journal title

The New England journal of medicine, 2021-12, Vol.385 (23), p.2207-2208

Language

English

Formats

Publication information

Publisher

United States: Massachusetts Medical Society

More information

Scope and Contents

Contents

To the Editor:
Given that the minimal clinically important difference in the percentage of predicted forced expiratory volume in 1 second (FEV
1
) is considered to be 5 percentage points,
1
the between-group difference of 3.5 percentage points in the percentage of predicted FEV
1
with elexacaftor–tezacaftor–ivacaftor, as compar...

Alternative Titles

Full title

Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2607578582

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2607578582

Other Identifiers

ISSN

0028-4793

E-ISSN

1533-4406

DOI

10.1056/NEJMc2115966

How to access this item