ClinConnect ClinConnect Logo
Search / Trial NCT04301856

Response to CFTR Modulators in CF Patients Under 18 Years

Launched by SOCIETE FRANCAISE DE LA MUCOVISCIDOSE · Mar 5, 2020

Trial Information

Current as of July 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at how well CFTR modulators—medications that help improve the function of a protein important for lung health—work in children with cystic fibrosis (CF) who are under 18 years old. The main goal is to see how the children's lung health changes after one year of treatment with these medications. The study will also monitor their health over the next few years, including how they grow, their quality of life, and any side effects from the medications.

To be eligible for this trial, children must be diagnosed with cystic fibrosis and currently receiving CFTR modulator therapy. Unfortunately, those over 18 years old or those who are pregnant or breastfeeding cannot participate. If your child joins this study, they'll undergo regular check-ups to assess their lung function and overall health, which will help doctors understand how these medications are working and if they are safe for young patients.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Children with cystic fibrosis under the age of 18 under CFTR modulator therapy
  • Exclusion Criteria:
  • Patients with cystic fibrosis without indication for CFTR modulator therapy
  • Patients over the age of 18
  • Pregnant or lactating women

About Societe Francaise De La Mucoviscidose

Société Française de la Mucoviscidose is a prominent organization dedicated to advancing the understanding, treatment, and management of cystic fibrosis (mucoviscidosis) in France. As a clinical trial sponsor, the organization plays a crucial role in facilitating research initiatives aimed at improving patient outcomes and enhancing therapeutic options for individuals affected by this genetic disorder. By collaborating with healthcare professionals, researchers, and patient advocacy groups, Société Française de la Mucoviscidose is committed to fostering innovation and supporting clinical studies that contribute to the global body of knowledge on cystic fibrosis, ultimately striving to improve the quality of life for patients and their families.

Locations

Paris, , France

Patients applied

0 patients applied

Trial Officials

Isabelle Sermet-Gaudelus, MD PhD

Principal Investigator

Société Francaise de la Mucoviscidose

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials