A Clinical Trial to Evaluate Efficacy and Safety of TransCon CNP Compared With Placebo in Infants (0 to <2 Years of Age) With Achondroplasia

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

A PHASE 2, MULTICENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED TRIAL, EVALUATING SAFETY, TOLERABILITY, AND EFFICACY OF SUBCUTANEOUS DOSES OF TRANSCON CNP ADMINISTERED ONCE WEEKLY FOR 52 WEEKS IN INFANTS (0 TO <2 YEARS OF AGE) WITH ACHONDROPLASIA FOLLOWED BY AN OPEN LABEL EXTENSION (OLE) PERIOD

Intervention/treatment:
NAVEPEGRITIDE (TRANSCON CNP)
Medical condition:
ACHONDROPLASIA
Protocol code:
ASND0030
Control number:
302955
Status:
Recruiting
Approved:
November 21, 2025
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT06079398
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
0 Years to 2 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Ascendis Registry Inquiries
Role
CONTACT
Phone:
+45 61242484
Sponsor
ASCENDIS PHARMA GROWTH DISORDERS A/S

Locations

Ascendis Investigational Site
Montreal, H3T 1C5
RECRUITING
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