drugset / Trial / NCT06308874
Investigate Safety, Tolerability, PK/PD of J2H-1702 in Healthy Females
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | J2H-1702 | Unknown | — | Oral |