30
Participants
Start Date
April 18, 2023
Primary Completion Date
January 31, 2026
Study Completion Date
January 31, 2026
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.
RECRUITING
The Emory Clinic, Atlanta
The Marcus Foundation
OTHER
Emory University
OTHER