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Completed Phase 3 Interventional Results available

Trial to Compare the Efficacy and Safety of NNC0195-0092 (Somapacitan) With Placebo and Norditropin® FlexPro® (Somatropin) in Adults With Growth Hormone Deficiency.

ClinicalTrials.gov ID: NCT02229851

Public ClinicalTrials.gov record NCT02229851. 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 30, 2026, 4:04 PM 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 Multicentre, Multinational, Randomised, Parallel-group, Placebo-controlled (Double Blind) and Active-controlled (Open) Trial to Compare the Efficacy and Safety of Once Weekly Dosing of NNC0195-0092 (Somapacitan) With Once Weekly Dosing of Placebo and Daily Norditropin® FlexPro® in Adults With Growth Hormone Deficiency for 35 Weeks, Followed by a 53-week Open-label Extension Period

Brief summary

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

This study is conducted globally. The purpose is to demonstrate the efficacy of once weekly dosing of NNC0195-0092 (somapacitan) compared to placebo and once-daily dosing of somatropin (human growth hormone, hGH) after 35 weeks of treatment in adults with growth hormone deficiency.

Study identification

NCT ID
NCT02229851
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
301 participants

Conditions and interventions

Eligibility (public fields only)

Age range
23 Years to 79 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
Oct 31, 2014 (Actual)
Primary completion
Apr 21, 2017 (Actual)
Completion
May 7, 2018 (Actual)
Last update posted
Nov 23, 2020

2014 – 2018

United States locations

U.S. sites
29
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Novo Nordisk Investigational Site Birmingham Alabama 35233 —
Novo Nordisk Investigational Site Los Angeles California 90033 —
Novo Nordisk Investigational Site Los Angeles California 90095 —
Novo Nordisk Investigational Site Aurora Colorado 80045 —
Novo Nordisk Investigational Site Atlanta Georgia 30318 —
Novo Nordisk Investigational Site Roswell Georgia 30076 —
Novo Nordisk Investigational Site Topeka Kansas 66606 —
Novo Nordisk Investigational Site Baltimore Maryland 21205 —
Novo Nordisk Investigational Site Boston Massachusetts 02114 —
Novo Nordisk Investigational Site East Lansing Michigan 48824 —
Novo Nordisk Investigational Site St Louis Missouri 63110 —
Novo Nordisk Investigational Site Omaha Nebraska 68105 —
Novo Nordisk Investigational Site Omaha Nebraska 68198-4120 —
Novo Nordisk Investigational Site Las Vegas Nevada 89128 —
Novo Nordisk Investigational Site Reno Nevada 89511 —
Novo Nordisk Investigational Site New York New York 10032 —
Novo Nordisk Investigational Site Cleveland Ohio 44195 —
Novo Nordisk Investigational Site Portland Oregon 97239 —
Novo Nordisk Investigational Site Philadelphia Pennsylvania 19104 —
Novo Nordisk Investigational Site Philadelphia Pennsylvania 19107 —
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15212 —
Novo Nordisk Investigational Site El Paso Texas 79935 —
Novo Nordisk Investigational Site Houston Texas 77030 —
Novo Nordisk Investigational Site Plano Texas 75093 —
Novo Nordisk Investigational Site San Antonio Texas 78229 —
Novo Nordisk Investigational Site Shavano Park Texas 78231 —
Novo Nordisk Investigational Site Salt Lake City Utah 84103 —
Novo Nordisk Investigational Site Federal Way Washington 98003 —
Novo Nordisk Investigational Site Seattle Washington 98122-5789 —

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 88 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02229851, 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 Nov 23, 2020 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02229851 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →