A Phase 2a, Randomized, Double-blind, Placebo-controlled, Incomplete Block Crossover Study to Evaluate the Safety and Efficacy of VX-371 Solution for Inhalation in Subjects With Primary Ciliary Dyskinesia
Clearing Lungs With Study Drug VX-371 Solution for Inhalation in Patients Primary Ciliary Dyskinesia
Sponsor: Vertex Pharmaceuticals Incorporated
Enrolling: Male and Female Patients
IRB Number: AAAQ8004
U.S. Govt. ID: NCT02871778
Contact: Sana Sajjad: 212-304-7969 / ss4901@cumc.columbia.edu
Additional Study Information: The purpose of this study is to find out if you can take the prescribed dose of VX-371 without problems, and whether VX-371 is safe and helps subjects with PCD. VX-371 is called an investigational or experimental drug because it has not been approved for use in people by the Food and Drug Administration (FDA), the branch of U.S. government which approves new drugs, or by any other regulatory agency in other countries. Inhaled HS is sometimes used to treat PCD patients. HS is extra-salty water that is sterile, so there are no germs in it. HS is also considered experimental in this study.
This study is closed
Angela DiMango, MD
Do You Qualify?
Has you or your child been diagnosed with Primary Ciliary Dyskinesia (PCD)? Yes No
You may be eligible for this study

Place Holder

For more information, please contact:
Sana Sajjad