Growth Hormone Deficiency Clinical Trial
Official title:
A Randomized, Double-blind, Vehicle-controlled, Parallel Group, Single Dose Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Three Doses of Long Acting HGH Product (MOD-4023) in Healthy Caucasian and Japanese Volunteers
The study is a Phase 1, randomized, double-blind, vehicle-controlled, single-dose, three dose
levels study in healthy Caucasian and Japanese male volunteers.
Following a 4-week screening period, eligible male subjects will be stratified by ethnic
group and will be randomized to one of six groups. On dosing day, designated as Day 1, each
subject will receive single SC injection of study medication according to group allocation
and will be followed up for a month for safety monitoring.
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