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 prioritisationProgramme:Technology appraisal guidanceExpected 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 prioritisationProgramme:Technology appraisal guidanceExpected publication date: TBC
CFHealthHub for managing cystic fibrosis during the COVID-19 pandemicStatus:Topic prioritisationProgramme:Medical technologies guidanceExpected publication date: TBC
Ivacaftor–tezacaftor–elaxcaftor and ivacaftor for treating cystic fibrosis with at least 1 F508del mutation in the CFTR gene in people 1 to under 2 years [TSID12295]Status:Topic prioritisationProgramme:Technology appraisal guidanceExpected publication date: TBC
Vanzacaftor–tezacaftor–deutivacaftor for treating cystic fibrosis with 1 or more responsive mutations in the CFTR gene in people 2 to 5 years [TSID12296]Status:Topic prioritisationProgramme:Technology appraisal guidanceExpected publication date: TBC