Expired Study
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Evansville, Indiana 47710


Purpose:

This trial is conducted in United States of America (USA). The aim of this trial is to examine the bioequivalence of Norditropin® versus Genotropin® in healthy adult volunteers.


Criteria:

Inclusion Criteria: - Body mass index (BMI) 18.0-27.0 kg/m^2 (both inclusive) - Considered generally healthy upon completion of medical history, physical examination, vital signs, screening laboratory results, and electrocardiogram (ECG), as judged by the Investigator (trial physician) Exclusion Criteria: - The receipt of any investigational medicinal product within 1 month prior to this trial - Current or previous treatment with growth hormone or IGF-I (insulin-like growth factor-I) - Female of childbearing potential who is pregnant, breast-feeding or intends to become pregnant or is not using adequate contraceptive methods (adequate contraceptive measures as required by local law or practice) for the duration of the trial - Known presence or history of malignancy - Diabetes mellitus - Use of pharmacologic doses of glucocorticoids - Use of anabolic steroids - History of drug or alcohol abuse


NCT ID:

NCT01401244


Primary Contact:

Study Director
Global Clinical Registry (GCR, 1452)
Novo Nordisk A/S


Backup Contact:

N/A


Location Contact:

Evansville, Indiana 47710
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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