Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Healthy Volunteers
Type
Interventional
Phase
Phase 1
Design
Allocation: RandomizedIntervention Model: Sequential AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 60 years
Gender
Both males and females

Description

A phase I, double-blind, placebo-controlled, single and multiple dose

A phase I, double-blind, placebo-controlled, single and multiple dose

Tracking Information

NCT #
NCT04817202
Collaborators
Not Provided
Investigators
Principal Investigator: +61-8-70887900 Wabnitz, phD CMAX Clinical Research Pty Ltd