誰が参加できますか

This study is seeking healthy male  participants, meaning that the participants will not have the condition being studied.

In addition to the criteria listed, participants must meet the following requirements:

  • Weight of 50 kg minimum
  • Body Mass Index of 17.5 - 30.5 kg/m2
  • Non-smoker, ex-smoker, smoker (max 5 cigarettes per day)
  • Women of non-childbearing potential
  • 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.

Condition
Healthy
The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.
Age
18-55 years
The age a person must be to participate in a clinical trial.
Sex
Males and females
The sex of people who may participate in a clinical trial. Sex is a person's classification based on assignment at birth. Eligibility based on sex is distinct from eligibility based on gender.
もっと参加基準を表示する

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.

実施項目

The study is planned to last for approximately 13 weeks. Several examinations or procedures will be required in connection with the study:

• A screening examination

• 3 treatment periods organised of 6 days and 5 nights in the PCRU (from Day -1 to Day 5). The 3 treatment periods will be separated by an interval of at least 14 days between dosing days.

• An on-site visit will take place on Day 7 of each period.

• The follow-up phone call will take place approximately 28-35 days after the last administration of the study medicine.

 

You will not personally derive any benefit from your participation in this study, but the results obtained could be very important for the development of medicines and treatments which will benefit other people.

Required overnight stays
3 periods of 5 nights
A participant may be required to stay overnight at the PCRU for observation and study procedures. The number and length of overnight stays is determined by the design of the study.
How long is this study?
Approximately 13 semaines
The length of the study includes the time from screening until the final follow-up call or study activity. There may be up to 28 days between screening and dosing.
Compensation
€ 2900 + € 450 additional COVID inconvenience fees upon completion of the study, plus transportation expenses 
Participants in clinical trials at the PCRU receive financial compensation for their participation. The amount depends on factors like length of the stay, total number of study visits, and the nature of the study procedures.

Interested in participating?

この治験についての詳しい情報:

0800.99.256 (フリーダイヤル:ベルギーから)、00800.26.36.26.36(フリーダイヤル:イギリス、フランス、ドイツ、オランダから)、+32.25.66.78.46(有料ダイヤル:上記以外の国から)に電話し、担当者に詳細をお問い合わせください。または、以下の登録フォームに入力してご送信ください。

「個人情報」とは名前、生年月日、電話番号、健康状態や病状など、一個人としてのあなたに関する情報を意味します。登録フォームに登録される際に当社と共有される個人情報は、医療アンケートや関連資料を送信するためにPCRUブリュッセルによって収集されます。

あなたの個人情報は、厳密に機密扱いで取り扱われ、適応されるすべての法律、特に治験に関するEUとベルギーの法律およびEUとベルギーの個人情報保護に関する法律に準拠して処理されます。

個人情報保護は私たち治験ユニットにとっても非常に重要です、そのため、https://privacycenter.pfizer.com/en/belgiumよりプライバシーに関する通知をお読みください。