A Phase 2a randomized, double-blind, placebo-controlled proof-of-concept study to evaluate the safety, tolerability, pharmacodynamics, and pharmacokinetics of SION-719 when added to physician-prescribed Trikafta™ in people with cystic fibrosis who are homozygous for the F508del mutation

Date Added
November 20th, 2025
PRO Number
Pro00147883
Researcher
Christina Mingora

List of Studies

Keywords
Cystic Fibrosis, Lung, Pulmonary
Summary

The purpose of this research study is to assess if the study drug SION-719 is safe and well-tolerated in people with cystic fibrosis who are already taking Trikafta, understand the effect of SION-719 on the body by measuring chloride levels, and to learn how the body absorbs, distributes, and gets rid of the study drug in people with cystic fibrosis. This study is a placebo controlled cross-over study with two study treatment periods, and participants will take part in both study treatment periods. Participants will be assigned either study drug or placebo. Participants will remain on standard dose of physician-prescribed Trikafta throughout the study. This study will be approximately 16 weeks, or 112 days long.

Institution
MUSC
Recruitment Contact
Rohini Rao
8437926109
recuitment@musc.edu



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