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Study to Evaluate the Tolerance and Pharmacokinetics of Suramin Sodium

Hand, Foot and Mouth Disease Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled, Single-dose, Dose-escalation Study to Evaluate the Tolerance and Pharmacokinetics of Suramin Sodium in Healthy Chinese Adults

Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled, single-dose with three incremental doses, Phase 1 study to evaluate the tolerance and pharmacokinetics of suramin sodium for injection in Chinese healthy adults.

Clinical Trial Description

A total of 36 subjects are divided into three dosage groups: 10mg/kg, 15mg/kg and 20mg/kg, in which 20mg/kg is the conventional dosage per international pharmacopoeias for established indications of suramin sodium. Each dose group contains 12 subjects. By randomization, 10 of them receive suramin sodium while 2 of them receive placebo (0.9% sodium chloride injection）. The trial will start from the low dose (10mg/kg) group, followed by the middle dose (15mg/kg) and high dose (20mg/kg) groups, only after the safety in the previous dose group has been demonstrated.

All subjects in each dose group will be un-blinded after blood/urine collection and safety evaluation on Day 28. After that, blood and urine samples on suramin-dosing subjects will continue to collect on Days 56、84、112 and 140.

Subjects receiving placebo will complete the study on Day 28 if no AE is observed, or follow up till the adverse event (AE) return to normal or stabilize if AE is detected.

Blood and urine samples will be tested by a validated LC/MS method for pharmacokinetic study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03804749
Study type Interventional
Source First Affiliated Hospital of Zhejiang University
Contact Jianzhong Shentu, Ph.D.(Pharm)
Phone 0571 87236560
Email stjz@zju.edu.cn
Status Recruiting
Phase Phase 1
Start date December 19, 2018
Completion date December 19, 2020
View Details
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