Chengdu Xinhua Hospital
Chengdu, Sichuan, 610000, China
NCT Number: NCT06385145
The purpose of this study is to compare the pharmacokinetics of the two different PEG-rhGH preparations.
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Notify Me18 year–45 year
Male
Interventional
Phase 1
Chengdu, Sichuan, 610000, China
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A single subcutaneous injection of PEG-rhGH with new preparation
A single subcutaneous injection of PEG-rhGH with present preparation
Time frame: 0 hours -192 hours post-administration
Time frame: 0 hours -192 hours post-administration
Time frame: 0 hours -192hours post-administration
Time frame: up to approximately 30 days
Time frame: 0 hours -192 hours post-administration
Time frame: 0 hours -192 hours post-administration
Time frame: 0 hours -192 hours post-administration
Changchun GeneScience Pharmaceutical Co., Ltd.
Industry
A Randomized, Open-label, Single Dose, 2-period Crossover Bioavailability Study of Two Different Polyethylene Glycol Recombinant Human Growth Hormone(PEG-rhGH) Preparations in Chinese Healthy Adult Male Subjects
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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