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A Phase 2 Clinical Trial to Evaluate Efficacy, Safety, and Tolerability of Navepegritide in Combination With Lonapegsomatropin in Children With Achondroplasia — COACH  

Achondroplasia Clinical Trial

Official title:
A Phase 2, Open-Label, Single-Arm, 156-week Trial to Investigate the Efficacy, Safety and Tolerability of Combined Once Weekly Navepegritide and Lonapegsomatropin in Children With Achondroplasia

Clinical Trial Summary

This proof-of-concept trial is being conducted to evaluate the efficacy, safety and tolerability of combination treatment with navepegritide and lonapegsomatropin administered as separate subcutaneous (SC) injections once weekly in children with achondroplasia (ACH) aged 2 to 11 years.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06433557
Study type Interventional
Source Ascendis Pharma A/S
Contact Vibeke Breinholt
Phone +4561242484
Email vib@ascendispharma.com
Status Not yet recruiting
Phase Phase 2
Start date June 2024
Completion date July 2027
View Details
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