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NCT05308927

French Registry of Children Treated With Norditropin® for Short Stature Associated With Noonan Syndrome

ENROLLING BY INVITATION Last updated 25 September 2025
What this trial tests

trial testing Norditropin in Noonan Syndrome in 221 participants. Enrolling by invitation.

Timeline
16 March 2022
Primary endpoint
17 March 2028
17 March 2028

Quick facts

Lead sponsorNovo Nordisk A/S
StatusENROLLING BY INVITATION
Study typeOBSERVATIONAL
Enrollment221
Start date16 March 2022
Primary completion17 March 2028
Estimated completion17 March 2028
Sites3 locations across France

Drugs / interventions tested

Conditions studied

Sponsor

Novo Nordisk A/S — full company profile →

Who can join

Eligibility, any sex, with Noonan Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a non-interventional registry of children treated with Norditropin® for short stature due to Noonan Syndrome (NS). This study aims to provide data on long-term growth evolution and safety of Norditropin® as well as Health Related Quality of Life (HRQoL) data. This registry will include the entirety of children treated with Norditropin® for short stature due to NS over the inclusion period. The decision to initiate treatment with commercially available Norditropin® is made by the patient/parents/Legally Acceptable Representative (LAR) and the treating physician before and independently from the decision to include the patient in this study.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Norditropin

Trials testing the same drug.

Other recruiting trials for Noonan Syndrome

Currently open trials in the same condition.

Other Novo Nordisk A/S trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05308927.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing