Participate in innovative clinical trials for asthma and gain access to potential new treatments not available elsewhere. Our studies provide personalized care from experienced medical professionals, guiding you through each step.
Your participation can make a real difference—for yourself and for others affected by asthma. By contributing to medical research, you help advance treatments that could improve lives and shape the future of asthma care.
These research studies are designed for adults and adolescents living with asthma. The studies are testing medications to see if they can help reduce the risk of asthma flare-ups. Additional goals are to assess how safe the study drugs are and how they are processed by the body compared to placebos.
The studies will consist of a screening period, a treatment period, and a follow-up period. The length of the studies varies depending on which study you qualify for and choose to participate in. If you qualify and choose to participate, you may earn compensation for your study-related time and travel. Throughout the study, your health and progress will be closely monitored by the study team. Your participation could help advance research in asthma care.
Those who qualify and choose to participate could receive:
Access to the study
medication at no cost
Access to our top-tier team of board-certified physicians
at no cost
Compensation for study-related time and travel.
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 approved 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.