See if You Qualify

Fill out the form below to see if you meet the basic study requirements.

Who are we looking for?

To qualify for participation in the Abdominal Fat Reduction Study, individuals should have a body weight within the range of average to slightly overweight and maintain good overall health & a stable lifestyle, with belly fat that does not fold when standing. As part of this study, participants will be required to undergo MRI scans and receive up to four sets of injections, administered once every three weeks, at one of our designated research sites. Additionally, individuals must commit to attending scheduled screening and checkup appointments.

What is the purpose of this study?

Traditional methods of reducing abdominal fat through cosmetic procedures frequently involve surgical or invasive interventions. At Caliway Biopharmaceuticals, researchers are testing a potential alternative – a non-invasive option consisting of a series of injections.

Early investigations into these investigational injections have displayed encouraging outcomes, both in terms of reducing abdominal fat and ensuring safety. This study represents a continuation of that research.

Frequently asked questions

What is the purpose of this treatment?

This investigational treatment may help to assist individuals dealing with surplus abdominal fat, offering them a pathway to attain their desired body composition without resorting to the extreme measures associated with invasive surgery.

What is the goal of this study?

To evaluate the efficacy of the investigational injections in reducing abdominal fat when compared to a placebo.

Where is this study taking place?

We have study locations available in the following cities: (city list)

How many people will be receiving the placebo?

25% of the people enrolled in the study will receive the placebo.

How long is my participation?

From start to finish, the study participation is about 21 weeks. The screening period is about 4 weeks. You could receive up to 4 treatments (3 weeks apart each). The treatment period is roughly 2 and a half months, or 10 weeks. Then the follow-up period is about 2 months, or 8 weeks.

Is there compensation for my participation?

Compensation is available for time and participation, but exact amounts vary by participating study site. Please ask your local study site for more details.

Is participation voluntary?

Your participation is entirely voluntary and can be ended at any time.