UnknownPhase 2NCT05246033
A Dose Escalation Trial Evaluating Safety, Efficacy, and Pharmacokinetics of Multiple Subcutaneous Doses of TransCon CNP Administered Once Weekly in Children With Achondroplasia
Studying Achondroplasia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Ascendis Pharma A/S
- Principal Investigator
- Vibeke BreinholtAscendis Pharma
- Intervention
- TransCon CNP(drug)
- Enrollment
- 24 enrolled
- Eligibility
- 2-10 years · All sexes
- Timeline
- 2022 – 2024
Study locations (5)
- Ascendis Pharma Investigational Site, Beijing, China
- Ascendis Pharma Investigational Site, Guangzhou, China
- Ascendis Pharma Investigational Site, Hangzhou, China
- Ascendis Pharma Investigational Site, Shanghai, China
- Ascendis Pharma Investigational Site, Wuhan, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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