drugset / Trial / NCT03908242

Phase I Study of Continuous Administration of Salvianolic Acid A Tablet

NCT03908242 ↗

Phase 1 Unknown 24 enrolled Peking University First Hospital
RandomizedParallel-groupTriple-blindTreatment

Summary

Salvianolic acid A has a variety of pharmacological effects, such as: anti-oxidation, scavenging oxygen free radicals, anti-fibrosis, anti-myocardial ischemia, anti-coagulation, anti-thrombosis, anti-tumor, etc. Professor Du Guanhua, at Institue of Materia Medica, Chinese Academy of Medical Sciences, first discovered that salvianolic acid A can alleviate diabetic complications and improve patients' quality of life. With the support of major national science and technology projects, the preclinical research work of salvianolic acid A was completed, and the application was approved by the State Food and Drug Administration (Clinical Approval No.: 2016L06293).The purpose of this study is to assess the safety,tolerability, and pharmacokinetics (PK) of an extended dosing regimen ofsalvianolic acid A: open label, continuous subcutaneous infusion for 7 days were tested as ascending doses of salvianolic acid A from 90mg up to 180 mg.

Timeline

Start
2019-04-08
Primary completion
2019-04-30
Completion
2019-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject salvianolic acid A Small molecule 90 mg Subcutaneous
Subject salvianolic acid A Small molecule 180 mg Subcutaneous

Indications