Products - Cystic fibrosis | Topic | NICE

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Showing 13 products

Date | Title

Ivacaftor–tezacaftor–elexacaftor, tezacaftor–ivacaftor and lumacaftor–ivacaftor for treating cystic fibrosis (TA988)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
24 July 2024
Cystic fibrosis: diagnosis and management (NG78)
Product type:
Guidance
Programme:
NICE guideline
Published:
25 October 2017
Colistimethate sodium and tobramycin dry powders for inhalation for treating pseudomonas lung infection in cystic fibrosis (TA276)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 March 2013
Mannitol dry powder for inhalation for treating cystic fibrosis (TA266)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 November 2012
CFHealthHub for managing cystic fibrosis during the COVID-19 pandemic (MIB219)
Product type:
Advice
Programme:
Medtech innovation briefing
Published:
10 July 2020
OxyMask for delivering oxygen therapy (MIB160)
Product type:
Advice
Programme:
Medtech innovation briefing
Published:
27 September 2018
Cystic fibrosis (QS168)
Product type:
Quality standard
Published:
18 May 2018
Vanzacaftor–tezacaftor–deutivacaftor for treating cystic fibrosis with 1 or more F508del mutations in the CFTR gene in people aged 6 years and over [ID6372]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
21 August 2025
Elexacaftor–tezacaftor–ivacaftor and ivacaftor for treating cystic fibrosis with at least 1 F508del mutation in the CFTR gene in children aged 2 to 5 [TSID10767]
Status:
Topic selection
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Elexacaftor–tezacaftor–ivacaftor with ivacaftor for treating cystic fibrosis without an F508del mutation and with a mutation in the CFTR gene that is responsive to elexacaftor–tezacaftor–ivacaftor in people aged 6 and over [TSID11847]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ivacaftor for treating cystic fibrosis with mutations in the CFTR gene in babies and children aged 1 to 3 months or weighing 3 kg to 24 kg [TSID11894]
Status:
Topic selection
Programme:
Technology appraisal guidance
Expected publication date:
TBC
CFHealthHub for managing cystic fibrosis during the COVID-19 pandemic
Status:
Topic selection
Programme:
Medical technologies guidance
Expected publication date:
TBC
Brensocatib for treating moderate to severe non-cystic fibrosis bronchiectasis in people 12 years and over [ID6448]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC