drugset / Trial / NCT03071081

Study for Safety and Tolerability of TOP1288 Administered Orally in Healthy Subjects

NCT03071081 ↗

Phase 1 Completed 37 enrolled Topivert Pharma Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study evaluates the safety and tolerability of TOP1288 oral single ascending and multiple doses in healthy subjects.

Timeline

Start
2017-02-08
Primary completion
2017-06-02
Completion
2017-06-02

Drugs

EvaluationDrugModalityDoseRoute
Subject TOP1288 Small molecule 200 mg Oral
Subject TOP1288 Small molecule 1 g Oral

Indications