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A Multicentre, Randomised, Open-labelled, Parallel-group, Activecontrolled Trial to Evaluate the Safety of Once Weekly Dosing of Somapacitan (NNC0195-0092) and Daily Norditropin® FlexPro® for 52 Weeks in Previously Human Growth Hormone Treated Japanese Adults With Growth Hormone Deficiency
This trial is conducted in Asia. The aim of this trial is to evaluate the safety of once weekly dosing of somapacitan (NNC0195-0092) and daily Norditropin® FlexPro® for 52 weeks in previously human growth hormone treated Japanese adults with growth hormone deficiency.
Age
18 - 79 years
Sex
ALL
Healthy Volunteers
No
Novo Nordisk Investigational Site
Bunkyo-ku, Tokyo, Japan
Novo Nordisk Investigational Site
Chiba-shi, Chiba, Japan
Novo Nordisk Investigational Site
Fukuoka, Japan
Novo Nordisk Investigational Site
Kagoshima, Japan
Novo Nordisk Investigational Site
Kobe, Hyogo, Japan
Novo Nordisk Investigational Site
Kyoto-shi Kyoto, Japan
Novo Nordisk Investigational Site
Okayama, Okayama, Japan
Novo Nordisk Investigational Site
Osaka, Japan
Novo Nordisk Investigational Site
Sagamihara-shi, Kanagawa, Japan
Novo Nordisk Investigational Site
Tokyo, Japan
Start Date
March 3, 2017
Primary Completion Date
October 4, 2018
Completion Date
October 4, 2018
Last Updated
November 23, 2020
62
ACTUAL participants
somapacitan
DRUG
Norditropin
DRUG
Lead Sponsor
Novo Nordisk A/S
NCT05230550
NCT07259564
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT01514500