drugset / Trial / NCT04164121

A Clinical Study Trial of Phenlarmide in China

NCT04164121 ↗

Phase 1 Completed 36 enrolled Yiling Pharmaceutical Inc.
RandomizedParallel-groupQuadruple-blindOther

Summary

1. To evaluate the tolerance and safety of FLA tablets in healthy volunteers. 2. To evaluate the pharmacokinetics of FLA tablets in healthy volunteers. 3. Provide basis for dosage setting for follow-up clinical research.

Timeline

Start
2019-12-17
Primary completion
2020-12-02
Completion
2020-12-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Phenlarmide Unknown 150 mg Oral
Subject Phenlarmide Unknown 600 mg Oral
Subject Phenlarmide Unknown 900 mg Oral

Indications