Who may participate
This study is seeking healthy male and female participants, meaning that the participants will not have the condition being studied.
In addition to the criteria listed, participants must meet the following requirements:
- Be a woman of non-childbearing potential. This means that you are either post-menopausal or that you have been surgically sterilized.
- Be a woman of childbearing potential who fulfills one of the criteria listed below:
- Have had a bilateral tubal occlusion
- Have a non-hormonal IUD
- Have a hormonal IUS
- Have a partner who has undergone a vasectomy at least six months ago.
For Both Sexes:
- Have a minimum body weight of 50 kg
- Have body Mass Index of 25.0 - 40.0 kg/m2
- Be a non-smoker or a smoker who smokes a maximum of 5 cigarettes per day
- Be able to meet all study visit requirements
There are other requirements for participation in this study. The study staff will explain these to you during the screening process.
Each clinical study has its own guidelines for who can participate, called eligibility criteria. However, only the research study staff can fully determine if you qualify to enroll in the study.
What to expect
The study is planned to last for approximately 10 weeks. There are several examinations procedures will be required in connection with the study:
- A screening examination
- A hospitalisation period of 7 days (6 nights)
- A follow-up phone call
Each participant will have a follow-up phone call 28 to 35 days after administration of the last dose of study medicine.
€ 1350 + € 180 additional COVID fees for participation, plus transportation expenses
Interested in participating?
New to clinical research? If you’re interested in becoming a participant or need more information on the registration process, please complete and submit the registration form. We will contact you as soon as possible
Already in our database? If you’d like to subscribe for this study, please contact us by phone.
Studies (recruiters) For more information, call 0800/99.256 (from abroad: 0032/2. 556.70.02 or 00800/2636.2636 from France, The Netherlands, Germany, UK) or email us.
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The personal data you share with us when completing the registration form is collected by the Brussels PCRU in order to send you the relevant literature and the medical questionnaire. It will be processed in a strictly confidential manner and in conformity with all applicable legislations, especially the European and Belgian laws applicable to clinical trials, and the European and Belgian laws applicable to personal data protection.
Personal data protection is very important to our clinical research unit. That’s why we ask that you read our Privacy Notice available at https://privacycenter.pfizer.com/en/belgium.