Ivacaftor / Tezacaftor / Elexacaftor (5) – Kaftrio®

• Clinical trials
  • For the assessment of the additional benefit of IVA/TEZ/ELX + IVA for the treatment of people aged 12 years and over with cystic fibrosis who are heterozygous for the F508del mutation in the CFTR gene and who have a mutation on the second allele that is neither a minimal-function mutation, nor a gating mutation (including R117H)or residual function mutation, or in whom the mutation on the second allele is unknown (other mutations), the pharmaceutical manufacturer has not submitted any study data.

Individuals aged 12 years and over with cystic fibrosis who are heterozygous for the F508del mutation in the CFTR gene and who have a mutation on the second allele that is neither a minimal function mutation, nor a gating mutation (including R117H)or residual function mutation, or in whom the mutation on the second allele is unknown (other mutations)

• An additional benefit is not proven.
• Overall, the pharmaceutical manufacturer did not submit any study for the present therapeutic indication that would have been suitable for assessing the additional benefit of IVA/TEZ/ELX + IVA compared with the appropriate comparator therapy.
• An additional benefit of IVA/TEZ/ELX + IVA compared with the appropriate comparator therapy is not proven.
• Taking into account the available evidence on the medical benefit of IVA/TEZ/ELX + IVA, the progressive course of the disease and the statements from medical societies regarding the current reality of care, ivacaftor/tezacaftor/Elexacaftor in combination with Ivacaftor may represent a relevant treatment option for patients aged 12 years and over who are heterozygous for the F508del mutation in the CFTR gene and have an unknown or other mutation on the second allele.

Courtesy translation only, please refer to the German original.