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

NCT04235140

Phase 3 Completed 52 enrolled Vertex Pharmaceuticals Incorporated
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

Drugs

EvaluationDrugModalityDoseRoute
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

Indications