Interested in Participating in a Trial for People with Ragweed Allergies?
This clinical research study is looking at the safety and effectiveness of an investigational medication option for people who suffer from symptoms associated with ragweed allergies. Study volunteers will be compensated with up to $1,720 for their time and effort.
Would you like to take part?
As a volunteer in a research study, you’ll receive medical care related to the study from the study doctor, and regular follow up to monitor the effectiveness of the care you’ll receive. The results of this research will be used to find out if the experimental medication being studied will be of benefit to others or not. Study volunteers are an important part of moving medical care forward.
You may qualify to participate in this study if you:
- Are male or female, 18 years of age or older
- Are voluntarily willing and able to follow instructions, and can travel to participate in a Phase 3 Clinical trial at Cliantha Research Mississauga
- Have at least a two-year history of moderate-to-severe ragweed-induced allergic conjunctivitis based on the investigator’s judgement
You may not qualify to participate if you:
- Are a pregnant female or plan to become pregnant during the duration of the study
- Have a history of anaphylaxis to any allergen being tested
- Have a history of glaucoma or have had ocular surgery within the past 12 months
- Have a history of uveitis in the past 3 years
- Have a history of moderate-to-severe asthma
- Have any other clinically significant condition that could endanger your health during the course of the study
There are other eligibility requirements that the study doctor will review. Only the study doctor can finally determine whether you are eligible to participate in the study or not.
