Participating in a clinical trial may seem intimidating and confusing, but our experienced physicians and research coordinators ensure that all participants are fully informed and comfortable throughout the entire process. Learn more about clinical trials below!

What is a clinical trial?

The goal of clinical trials is to test new medications and therapies before they are made available to the public. Through Phase I-IV trials, the treatment under research (the investigational product) is tested for its effectiveness, potential side effects, and safest dosage. All clinical studies are FDA approved and are continuously supervised by the Institutional Review Board, pharmaceutical companies, and medical monitors.

What is the Informed Consent FORM and California Bill of Rights for clinical trials?

The Informed Consent Form and California Bill of Rights explains the main purpose of the study, possible risks and benefits of the medication, schedule of appointments, types of procedures, and your rights as a participant in a clinical trial. Before the start of any study-related procedures, you will be given time to read, review, and sign these documents. During this process, our physicians and research coordinators will also be available to supplement your understanding of the study and answer all questions.

are clinical studies right for me? Am I eligible to qualify?

Many patients volunteer for clinical trials because their current medications are too expensive. Some come as a last resort for their illness as all other treatments have failed. Others want to contribute to the fast-growing field of medicine. We welcome anyone who is qualified and dedicated to improving medical care for themselves and others.
Each study is different and has their own set of eligibility requirements. These requirements include, but are not limited to age, gender, and medical history.

What should I consider before agreeing to participate in clinical studies?

Make sure you have the time and means of travel to attend your appointments. Visits vary depending on the study but are generally one hour. The initial visit will take longer due to the consenting process. Some studies may require more time or overnight visits.

Does it cost me anything? Do I get paid?

Volunteers do not need to pay anything to participate in our clinical studies. Instead, participants receive compensation for enrolling in our studies, even if you fail the screening visit! Compensation ranges from as much as $250.00 to $4,500.00! We even provide snacks and entertainment for any visit that takes longer than two hours to complete!

Will my information stay confidential?

Yes, clinical trials follow HIPAA (Health Insurance Portability and Accountability Act of 1996). All identifying information is omitted when data is relayed to the pharmaceutical company.