A Phase 2 Clinical Trial to Evaluate Efficacy, Safety, & Tolerability of

See also
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Enrolling by invitation	`NCT05929807` - A Clinical Trial to Investigate Long-term Safety, Tolerability, and Efficacy of Weekly Subcutaneous Doses With TransCon CNP in Children and Adolescents With Achondroplasia	Phase 2/Phase 3
Completed	`NCT03875534` - A Multi-center, Longitudinal, Observational Study of Children With Achondroplasia
Terminated	`NCT03794609` - Observational Study Investigating Clinical & Anthropometric Characteristics of Children With Achondroplasia.
Completed	`NCT03583697` - A Clinical Trial to Evaluate the Safety and Efficacy of BMN 111 in Infants and Young Children With Achondroplasia	Phase 2
Active, not recruiting	`NCT03989947` - An Extension Study to Evaluate Safety and Efficacy of BMN 111 in Children With Achondroplasia	Phase 2
Active, not recruiting	`NCT05246033` - A Dose Escalation Trial Evaluating Safety, Efficacy, and Pharmacokinetics of Multiple Subcutaneous Doses of TransCon CNP Administered Once Weekly in Children With Achondroplasia	Phase 2

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

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

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms