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NCT07924059
Phase 3 Clinical Trial Evaluating the Efficacy and Safety of Navepegritide and Lonapegsomatropin in Achondroplasia
Conditions: Achondroplasia
Sex: All
Ages: 2 Years – 17 Years
Healthy volunteers: No
Phase: PHASE3
Enrollment: 144
Sponsor: Ascendis Pharma A/S
Summary
This pivotal trial is being conducted to evaluate the efficacy, safety and tolerability of dual therapy with navepegritide and lonapegsomatropin administered as separate subcutaneous (SC) injections once weekly in children with achondroplasia (ACH) aged 2 to 17 years.
Eligibility Criteria
Inclusion Criteria:
* 1\. Age 2 to \
Source: ClinicalTrials.gov (NCT07924059). StuddyBuddy aggregates publicly available trial information.