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Clinical Trial Summary

- Objectives: Primary objective_To evaluate the safety and tolerability after single oral administration of the investigational product (IP), J2H-1702 in healthy female subjects. Secondary objective_To evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) characteristics after single oral administration of the IP, J2H-1702 in healthy female subjects.


Clinical Trial Description

- Study Methodology: 6 Subjects will be randomized to the study group (J2H-1702 group) and 2 subjects will be to the placebo group. AE, VS, ECG, Lab tests will be evaluated to check the safety, tolerability and PK/PD. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06308874
Study type Interventional
Source J2H Biotech
Contact
Status Completed
Phase Phase 1
Start date January 2, 2023
Completion date February 17, 2023

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