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A Study to Evaluate the Efficacy and Safety of Infigratinib in Children and Adolescents With Achondroplasia — PROPEL3  

Achondroplasia Clinical Trial

Official title:
A Phase 3, Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Infigratinib in Children 3 to <18 Years of Age With Achondroplasia: PROPEL 3

Clinical Trial Summary

This is a Phase 3, multicenter, double-blind, randomized, placebo-controlled study to evaluate the efficacy and safety of infigratinib in children and adolescents with achondroplasia (ACH) who have completed at least 26 weeks of participation in the QED-sponsored study PROPEL (QBGJ398-001).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06164951
Study type Interventional
Source QED Therapeutics, Inc.
Contact
Status Enrolling by invitation
Phase Phase 3
Start date November 10, 2023
Completion date April 30, 2026
View Details
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