Affiliated Hospital of Qingdao University
Qingdao, Shandong, 266000, China
NCT Number: NCT04554043
The primary objective of this study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of SHR7280 tablets in healthy subjects.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 1
Qingdao, Shandong, 266000, China
GNRH antagonists can be used to treat sex hormone-dependent diseases, and SHR7280 is an oral GNRH antagonist. The purpose of this study is to observe the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple oral doses of SHR7280 in healthy subjects.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
PART 1:
PART 2:
Exclusion criteria
PART 1
PART 2:
treatment
blank control
Time frame: Pre-dose to 28±2 days after dose administration
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit( 28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1 and Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 1
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 2
Time frame: At pre-defined intervals from initial dose through final study visit (28±2 days after dose administration)
Part 2
Jiangsu HengRui Medicine Co., Ltd.
Industry
A Randomized, Double-blind, Dose-escalation, Placebo-controlled Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Oral Doses of SHR7280 Tablets in Healthy Subjects.
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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