honeybee

Researchers


Healthy Volunteer Study

Cliantha Research, Clinical Research Organization (CRO)


The purpose of this study is to evaluate the safety and tolerability (able to bear) of the study drug and also to understand the extent of this study drug’s absorption, levels of study drug in your blood and effects of the study drug.

Eligibility Criteria


Male, Female

18 to 65 years old

In general good health

Not having used tobacco products or nicotine-containing products within 30 days prior to dosing

Not have a history of pituitary and/or adrenal gland diseases

Have a BMI (Body Mass Index) between 18 kg/m2 to 30 kg/m2 inclusive and weigh at least 50kg

Other criteria will be assessed

Study Tasks


Informed Consent Document (ICF)
Medical history and demographics
Measurement of vital signs and physical examination
Electrocardiogram (ECG) – a recording of the electrical activity of the heart
Tuberculin skin test will be performed to test for Tuberculosis
Other tasks will be outlined during the ICF process

Ethics


This study has been approved by Advarra Ethics Board

Keywords


Clinical trial
Healthy volunteer

Activity and Time


Investigational Medicine

Clinical Trial

Weekdays, Weekends, Overnight, Weeknights

6 days total, 4 sessions

The study will be approximately 34 days in total, including screening, Period 1, and Period 2. For both Period 1 and Period 2, you will be required to stay at the Cliantha Research facility for two overnight stays. There is a 10-day washout in between the two periods. After Period 2, one end-of study follow-up visit is required.

Compensation


Up to $2550

Study Address


4500 Dixie Rd Mississauga, Ontario, Canada, L4W 1N2

Posting date: Jan 5, 2021

Earn $2550