RecruitingPhase 2NCT06079398
A Clinical Trial to Evaluate Efficacy and Safety of TransCon CNP Compared With Placebo in Infants (0 to <2 Years of Age) 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
- Medical Director, MDAscendis Pharma A/S
- Intervention
- Navepegritide(drug)
- Enrollment
- 72 enrolled
- Eligibility
- 0-2 years · All sexes
- Timeline
- 2024 – 2028
Study locations (17)
- Ascendis Investigational Site, Saint Paul, Minnesota, United States
- Ascendis Investigational Site, Houston, Texas, United States
- Ascendis Investigational Site, Madison, Wisconsin, United States
- Ascendis Investigational Site, Parkville, Australia
- Ascendis Investigational Site, Linz, Austria
- Ascendis Investigational Site, Copenhagen, Denmark
- Ascendis Investigational Site, Helsinki, Finland
- Ascendis Investigational Site, Paris, France
- Ascendis Investigational Site, Berlin, Germany
- Ascendis Investigational Site, Cologne, Germany
- Ascendis Investigational Site, Dublin, Ireland
- Ascendis Investigational Site, Milan, Italy
- Ascendis Investigational Site, Auckland, New Zealand
- Ascendis Investigational Site, Oslo, Norway
- Ascendis Investigational Site, Coimbra, Portugal
- +2 more locations on ClinicalTrials.gov
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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