Project Description:
A Phase 3, randomized, double-blind, placebo-controlled, crossover study to evaluate eht efficacy and safety of Ivacaftor and VX-661 in combination with Ivacaftor in subjects aged 12 years and older with cystic fibrosis, heterozygous for the F508del-CFTR mutation, and a second Allele with CFTR mutation predicted to have residual function.
Core Function(s):
Performing Research or Evaluation
Area of Emphasis
Health-Related Activities
Target Audience:
Professionals and Para-Professionals
Unserved or Under-served Populations:
Racial or Ethnic Minorities, Disadvantaged Circumstances, Limited English, Geographic Areas
Primary Target Audience Geographic Descriptor:
National
COVID-19 Related Data:
N/A