drugset / Trial / NCT03650075

To Determine Safety and Tolerability of MG-S-2525 and to Evaluate Its PK Profile in Healthy Volunteers

NCT03650075 ↗

Phase 1 Completed 81 enrolled Metagone Biotech Inc.
RandomizedCrossoverDouble-blindTreatment

Summary

This is a Phase I stage to investigate the safety and tolerability of MG-S-2525 in healthy volunteers. The proposed trial consists of 3 study parts to be conducted at Tri-Service General Hospital and includes Single Ascending Dose (SAD), Multiple Ascending Dose (MAD) and Food Effect parts. This study will enroll up to 16 evaluable subjects in the SAD part, 36 evaluable subjects in the MAD part and enroll up to 20 evaluable subjects for the Food Effect part.

Timeline

Start
2019-02-25
Primary completion
2019-12-31
Completion
2020-02-27

Drugs

EvaluationDrugModalityDoseRoute
Subject MG-S-2525 Small molecule — Oral