Viewing StudyNCT00455260



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Last Modification Date: 2024-10-26 @ 9:31 AM
Study NCT ID: NCT00455260
Status: COMPLETED
Last Update Posted: 2013-09-02
First Post: 2007-04-02

Brief Title: A Multi-Dose Study to Assess Tolerability Safety and Pharmacology of hGH-ViaDerm System in Adults With GH-Deficiency
Sponsor:
Organization: Teva Branded Pharmaceutical Products RD Inc

Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: None
Bio Spec Description: None
Enrollment Count: 60
Enrollment Type: ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Name
PHASE1
Observational Models:
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