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Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled, multiple-ascending dose study of MS-553 in healthy volunteers. Endpoints are safety, tolerability, and pharmacokinetics. Subjects are dosed for 14 days.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Safety and PK in Healthy Volunteers

NCT number NCT02406989
Study type Interventional
Source MingSight Pharmaceuticals Pty Limited
Contact
Status Completed
Phase Phase 1
Start date April 2015
Completion date September 2015