Trikafta for Patients With Non-cystic Fibrosis Bronchiectasis

PHASE4RecruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

April 18, 2023

Primary Completion Date

January 31, 2026

Study Completion Date

January 31, 2026

Conditions
Non-cystic Fibrosis Bronchiectasis
Interventions
DRUG

Trikafta

Participants will be given elexacaftor 100 mg/tezacaftor 50 mg/ivacaftor 75 mg (two pills once daily in the morning) and ivacaftor 150 mg (once daily in the evening), as the FDA-registered agent, Trikafta. Dose and schedule will be for 28 days, and otherwise identical to what has already been FDA-approved for effective treatment of cystic fibrosis.

Trial Locations (1)

30322

RECRUITING

The Emory Clinic, Atlanta

All Listed Sponsors
collaborator

The Marcus Foundation

OTHER

lead

Emory University

OTHER