drugset / Trial / NCT04235140
Long-term Safety of Lumacaftor/Ivacaftor in Participants With Cystic Fibrosis Who Are Homozygous for F508del and 12 to <24 Months of Age at Treatment Initiation
NaSingle-groupOpen-labelTreatment
Summary
This is a Phase 3, multicenter, open-label and roll-over study in participants who are 12 to \<24 months of age at initiation of Lumacaftor/Ivacaftor (LUM/IVA) treatment.
Timeline
- Start
- 2020-02-24
- Primary completion
- 2023-08-22
- Completion
- 2023-08-22
Publications
- Heneghan M, Southern KW, Murphy J, Sinha IP, Nevitt SJ. Corrector therapies (with or without potentiators) for people with cystic fibrosis with class II CFTR gene variants (most commonly F508del). Cochrane Database Syst Rev. 2023 Nov 20;11(11):CD010966. doi: 10.1002/14651858.CD010966.pub4.
- Southern KW, Murphy J, Sinha IP, Nevitt SJ. Corrector therapies (with or without potentiators) for people with cystic fibrosis with class II CFTR gene variants (most commonly F508del). Cochrane Database Syst Rev. 2020 Dec 17;12(12):CD010966. doi: 10.1002/14651858.CD010966.pub3.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ivacaftor | Other / unclassified | 94 mg | Oral |
| Subject | Ivacaftor | Other / unclassified | 125 mg | Oral |
| Subject | Ivacaftor | Other / unclassified | 188 mg | Oral |
| Subject | Lumacaftor | Small molecule | 75 mg | Oral |
| Subject | Lumacaftor | Small molecule | 100 mg | Oral |
| Subject | Lumacaftor | Small molecule | 150 mg | Oral |