drugset / Trial / NCT06308874

Investigate Safety, Tolerability, PK/PD of J2H-1702 in Healthy Females

NCT06308874 ↗

Phase 1 Completed 16 enrolled J2H Biotech
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2023-01-02
Primary completion
2023-02-17
Completion
2023-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject J2H-1702 Unknown — Oral