Orkambi Treatment in 2 to 5 Year Old Children With CF

CompletedOBSERVATIONAL
Enrollment

28

Participants

Timeline

Start Date

April 10, 2019

Primary Completion Date

June 16, 2021

Study Completion Date

June 16, 2021

Conditions
Cystic Fibrosis
Interventions
DRUG

Orkambi

Orkambi is a novel approved therapy for use in people homozygous for the F508del mutation in the CFTR gene. It is a combination of lumacaftor (VX-809) and ivacaftor( VX-770) that addresses both the processing and gating defects of the F508del mutation. The small-molecule corrector lumacaftor corrects the F508del processing defect and increases epithelial delivery of CFTR protein1. Ivacaftor is a CFTR potentiator that increases the channel open probability in F508del-mutant CFTRs that undergo epithelial delivery in vitro and has an additive effect with lumacaftor on chloride transport (2,3,4,5).

Trial Locations (1)

19146

Children's Hospital of Philadelphia, Philadelphia

All Listed Sponsors
collaborator

Vertex Pharmaceuticals Incorporated

INDUSTRY

lead

Children's Hospital of Philadelphia

OTHER

NCT03795363 - Orkambi Treatment in 2 to 5 Year Old Children With CF | Biotech Hunter | Biotech Hunter