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Active, not recruiting Phase 3 Interventional

A Research Study to Compare Somapacitan Once a Week With Norditropin® Once a Day in Children Who Need Help to Grow

ClinicalTrials.gov ID: NCT05330325

Public ClinicalTrials.gov record NCT05330325. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 3:25 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study Comparing the Effect and Safety of Once Weekly Dosing of Somapacitan With Daily Norditropin® as Well as Evaluating Long-term Safety of Somapacitan in a Basket Study Design in Children With Short Stature Either Born Small for Gestational Age or With Turner Syndrome, Noonan Syndrome, or Idiopathic Short Stature

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The study compares two medicines for treatment of children born small and who stay small, or with Turner Syndrome, Noonan Syndrome, or idiopathic short stature. The purpose of the study is to see how well treatment with somapacitan works compared to treatment with Norditropin®. Somapacitan is a new medicine, and Norditropin® is a medicine doctors can already prescribe in some countries. The study will last for upto 5.5 years. The participants will either get somapacitan once a week up to 5.5 years or Norditropin® once a day for 1 year followed by somapacitan once a week for up to 4.5 years. Which treatment the participants get is decided by chance.

Study identification

NCT ID
NCT05330325
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
412 participants

Conditions and interventions

Eligibility (public fields only)

Age range
2 Years to 10 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 10, 2022 (Actual)
Primary completion
Aug 5, 2024 (Actual)
Completion
Oct 29, 2027 (Estimated)
Last update posted
Jun 12, 2026

2022 – 2027

United States locations

U.S. sites
35
U.S. states
24
U.S. cities
35
Facility City State ZIP Site status
Univ of AL at Birmingham_BRM Birmingham Alabama 35233 —
Children's Hospital Los Angeles - Endocrinology Los Angeles California 90027 —
Sutter Valley Med Fdt Ped Endo Sacramento California 95821 —
Rady Childrens Hosp San Diego San Diego California 92123 —
Children's Hospital Colorado Aurora Colorado 80045 —
Rocky Mt Ped and Endo Centennial Colorado 80112 —
Ped Endo Assoc PC-G.V Greenwood Village Colorado 80111-2803 —
Nemours/AI duPont Hosp-Chld Wilmington Delaware 19803 —
Childrens National Medical Ctr Washington D.C. District of Columbia 20010-2978 —
Nemours Chld Clnc Jacksonville Jacksonville Florida 32207 —
Atlanta Diabetes Associates Atlanta Georgia 30318 —
St. Luke's Children's Endo Boise Idaho 83712 —
Rocky Mt Clin Res, LLC Idaho Falls Idaho 83404-7596 —
Riley Hosp for Child-Indiana U Indianapolis Indiana 46202 —
University OF Iowa Iowa City Iowa 52242 —
UMass Medical School Worcester Massachusetts 01655 —
Univ of Minnesota M.C.H. Minneapolis Minnesota 55454 —
Children's Minnesota Saint Paul Minnesota 55102 —
Univ of Mississippi Med Ctr Jackson Mississippi 39216 —
The Children's Mercy Hospital Kansas City Missouri 64108 —
Goryeb Children's Hospital Morristown New Jersey 07962 —
UBMD Peds-Div of Endo/Diabetes Buffalo New York 14203 —
NYU Langone Hospital-LI Garden City New York 11530 —
NYU Langone Hospital-LI Mineola New York 11501 —
WakeMed Childn Endo-Dbt_Raleig Raleigh North Carolina 27610 —
Akron Children's Hospital Akron Ohio 44308 —
CCHMC_Cinc Cincinnati Ohio 45229 —
Univ Oklahoma Sci Ctr OK City Oklahoma City Oklahoma 73104 —
UPMC Child Hosp-Pittsburgh Pittsburgh Pennsylvania 15224 —
UT Southwestern Med Cntr Dallas Texas 75235 —
Cook Children's Medical Center Fort Worth Texas 76104 —
Consano Clinical Research, LLC Shavano Park Texas 78231 —
University Of Virginia Hospital Charlottesville Virginia 22903 —
MultiCare Inst for Res & Innov Tacoma Washington 98405 —
Marshfield Clinic Marshfield Wisconsin 54449 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 164 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05330325, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 12, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05330325 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →