The Pfizer New Haven Clinical Research Unit is conducting a clinical trial of an oral study drug for obesity and weight management. Part C of this study will look at the effects of the study drug combined with an additional oral medication.

Obesity is a chronic weight condition that increases the potential risk of other illnesses such as stroke and diabetes. By 2030, it is projected that over a billion people worldwide will be considered obese.

While the scientific and medical community defines obesity as a complex, multifactoral chronic disease requiring prevention and treatment efforts, there are still many misconceptions and stigma associated with this condition which can further impact patients’ quality of life and access to healthcare. Most people with obesity do not receive any treatment, and diet and lifestyle are often not effective at long-term weight management for many patients.

Read more about how you can help change lives as a healthy volunteer.

Who may participate

Every modern medical discovery starts with a clinical trial, and every clinical trial starts with the amazing people who volunteer.

This study is seeking healthy adult volunteers, meaning that the participants will not have the condition being studied and are in overall good health. In addition to the criteria listed, participants must meet the following requirements: 

  • Willing to take a study drug
  • Willing and able to come to our facility in New Haven, CT*
  • Willing and able to comply with all study procedures

*participants may be eligible to receive a bonus for travel, ask our staff for details

**females must be unable to bear children

There are other requirements for participation in this study. The study staff will explain these to you during the screening process.

Do you know someone who may meet these requirements? Refer a friend and you may be eligible to receive a bonus. 

Learn more

Condition

Healthy

Age

18-65 years

Sex

All sexes**

Referral bonus

Up to $200

Each clinical study has its own guidelines for who can participate, called eligibility criteria. However, only the research study staff can determine if you qualify to enroll in the study.

What to expect

If this study may be a fit for you, you’ll be invited to a screening visit at our facility in New Haven, CT. If you qualify for the study, there may be a period of up to 28 days before dosing.

If you choose to participate, you will stay at our facility for 12 overnights. During your stay, you will receive doses of the study drug and/or an additional medication on the following schedule:

  • A single dose of study drug daily in the morning for 10 days starting 2 days after admission
  • An additional dose of another medication alone or in addition to the study drug the day after admission, on the 3rd morning, and on the 11th morning.

All doses will be given orally after a standard breakfast.

Throughout the study, staff will closely monitor your health status and collect data, such as the levels of the study drug in your blood.

Download informed consent form

Required overnight stays

12 overnights

Long-term follow up

1 visit + 1 phone call

How long is this study?

About 39 days

Compensation

Up to $4,800 upon completion of the study

The PCRU Loyalty Program has arrived!

Our new Loyalty Program offers unique tiered gifts for new and returning participants.

 

Interested in participating?

Complete and submit this form, and a Pfizer New Haven Clinical Research Unit (PCRU) representative will contact you. Please note: volunteers completing this form must be able to read and speak English at an 8th grade level.

You may also call 1-800-254-6398 and speak with a PCRU representative to learn more.

For Japanese language assistance only, please call 1-833-711-9984. We apologize, our representatives cannot take calls in languages other than English or Japanese at this time.

The personal data gathered here will be collected, processed, and maintained in a confidential manner. Your information will be stored in our research unit’s database. We may use this information to invite you to participate in current and future clinical studies at the PCRU. You will have full access to your records at the Pfizer New Haven Clinical Research Unit and the opportunity to correct them if necessary.

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