Clinical Trial Services

Patients that choose the concierge-level services provided by Clinical Endpoints will enjoy the benefits of individual care and personalized service that is all too rare in healthcare settings today. We offer you a personalized visit to review your health concerns, discuss our available clinical trial treatment options, and provide care in a unique one-on-one setting where you will be isolated from other patients.

We are a leading center globally for the most promising and potentially life-saving clinical trial treatments offered by the world’s top-rated pharmaceutical companies. We specialize in offering additional options to patients that have exhausted traditional treatments and now seek new hope while wanting to contribute to discoveries that may aid their family, friends, and all humanity. We collaborate closely with your primary healthcare provider while providing you concierge-level service; we strive to personalize your care and deliver the best possible experience and outcome for you and your family.

A clinical trial is at the heart of all medical advances, which is how currently prescribed treatments were proven safe and effective for widespread therapeutic use. Clinical trials are studies designed to test how a new drug, surgical procedure or device works on a group of patient volunteers. A clinical trial evaluates the effectiveness and safety of new treatment options. The U.S. Food and Drug Administration (FDA) requires pharmaceutical companies to test new medications or devices in well-controlled and carefully monitored clinical trials before new treatments become widely available to physicians and their patients.

Participants in clinical trials play a more active role in their own healthcare and gain access to new research treatments before they become widely available. Many volunteers feel as though they are contributing to the potentially huge benefits of future treatments for those who may share their same medical condition. Others feel that due to new advances in drug treatments, a clinical trial may provide new hope and a chance at a brighter future. By participating in a clinical trial, volunteers benefit from free study-related medical procedures and study medications as well as closer attention from physicians and clinical research staff. Participants will also receive expert medical care for their specific condition.

Clinical trials follow strict regulations to protect the safety and rights of research volunteers. Each research site is mandated to follow strict ethical and legal regulations that are also monitored by the Food and Drug Administration (FDA). Following the FDA’s permission to conduct a clinical trial, an Institutional Review Board (IRB) comprised of medical professionals also evaluates the study to determine if it is safe and ethical for our volunteers. We will personally explain all of this to you in your first visit with us, before any commitment is made by you.

No, there is no cost to participate in a trial. All study-related exams and procedures will be done at no cost for the study participant. Typically, this means you will receive enhanced care for your condition. Additionally, many clinical trials may offer compensation for time and travel while participating in the new treatment study.

Yes, not only will you continue to see your Primary Care Provider, but we will coordinate and work very closely with your primary care physician if you consent to this communication.

See https://clinicaltrials.gov for more information on clinical trials.