Join our innovative clinical trial evaluating an investigational medication that is being researched to potentially help chronic weight management in adults who are overweight or obese, with cardiovascular disease.
Those who qualify and choose to participate may be compensated up to $3,730 for 20 in-clinic visits and 12 remote visits over approximately 3 years.
This study is designed to evaluate the safety and effectiveness of petrelintide, an investigational injection, for chronic weight management in adults who are overweight or obese, with cardiovascular disease. Petrelintide is an “investigational” drug because it has not been approved by the Food and Drug Administration (FDA).
The study is randomized, double-blind, and placebo-controlled to ensure high-quality, unbiased results. If you qualify and choose to participate, there is a 50% chance you will receive the study treatment and a 50% chance you will receive a placebo. A placebo is an inactive material that looks like the study drug but does not contain any active ingredient.
You will be in this study for at least 1 year and 7 months and up to 3 years which will include a screening period, a treatment period, and a follow up period. The study will require up to 20 in-clinic visits and 12 remote visits. If you qualify and choose to participate, you may be compensated up to $3,730 for your study-related time and travel. Your participation is entirely voluntary, and you can leave the study at any time.
Those who qualify and choose to participate could receive:
Access to the investigational study drug at no cost
Access to our top-tier team of board-certified physicians at no cost
Nutritional counseling at no cost
Compensation up to $3,730 for 20 in-clinic visits and 12 remote visits over approximately 3 years
A research study or clinical trial is the process a potential new drug, device, procedure, or process goes through to prove that it is safe, tolerable and effective for the condition it is being studied for. Research studies are the only way to advance medicine for future generations.
Each study has its own set of inclusion and exclusion criteria that a participant must meet before they are allowed to participate in a study. Patients from all backgrounds and walks of life are encouraged to participate.
Every participant in every research study must go through the informed consent process. During this, the trial doctor and research team go over what will happen in the study, what treatments you might get, how long the trial is expected to last, what happens during visits, the potential risks and benefits, and many other important facts about the study. Participants may withdraw their consent and discontinue the study at any time for any reason.
A placebo looks like a treatment but does not have any active medicine in it. Researchers use placebos to help make sure any changes in the participants’ health are actually caused by the study treatment. You do not get to choose if you get the study treatment or the placebo, and you may not know if you get the placebo until after the study. Not all research studies use a placebo.
If studies do not include diverse participants, we cannot know if treatments work for everyone who needs them. Studies only tell researchers how something works for the participants of that study, and they may not work the same in people of different races, ethnicities, ages, or sexes.
All research studies must follow federal laws and ethical guidelines, including HIPAA. Studies must also be reviewed by an expert group called an institutional review board (IRB) that helps make sure the trial is fair and as safe as possible, and that any risks to the participants are worth the potential benefits.