The Ruby Study is a clinical trial of a possible treatment for adults with gout who still have flare-ups despite taking allopurinol.
What is the RUBY Study?
The study will test how effective and safe a study drug called (dotinurad) may be in treating gout compared to allopurinol. Taking part in the study lasts about 18 months and includes 21 study visits (some by phone).
All participants will also receive a prescription for colchicine or a nonsteroidal anti-inflammatory drug (NSAID) to prevent flares. The cost of the prescription will be reimbursed.
Who may qualify to participate:
If you qualify, the study involves:
Have you been diagnosed with Psoriasis:
To qualify:
We will discuss the study details and review the eligibility criteria to see if you qualify for the study. We can also be contacted by email: studies@westcoastresearch.com.
About Clinical Trials
A clinical trial is a scientific study that tests the safety and effectiveness of a new medical treatment, drug, or device with patients. While years are spent in laboratory and animal research to determine the general use and safety of a new treatment, a clinical trial studies the exact effects on people.
A clinical trial may show that the investigational treatment is better than, as good as, or no better than the standard treatment for the same condition. Or it may confirm the discovery of a successful treatment of a health problem for which there had never been an adequate (successful) treatment.
A clinical trial is a partnership and a commitment between doctors and volunteer patients. It is the final test in a series of many carefully controlled scientific studies that are done to improve the quality of life.
The medical world cares about improving the quality of life through medical advances. That's why researchers constantly look for better or new ways of treating illness and disease. However, the general public cannot use their discoveries until they have conducted controlled testing on actual patients.
Clinical trials are the only way that testing can be done. The Food and Drug Administration (FDA) require clinical trials before it can approve a new treatment as safe and effective for public use.
West Coast Research is committed to protecting your privacy and maintaining the confidentiality of your personal and medical information. This Privacy Policy explains how we collect, use, and safeguard your data when you interact with our website, services, or participate in a clinical study. We may collect personal identification information such as your name, date of birth, and contact details, as well as health-related information like medical history, current medications, and study eligibility.
The information we collect is used to contact you about potential or ongoing clinical studies, determine your eligibility for participation, comply with regulatory requirements, and improve our outreach and services. West Coast Research does not sell your personal or medical information. Your data may be shared only with study sponsors, regulatory bodies, or authorized clinical research staff when necessary and in accordance with the law. All third parties are required to protect your information with the same level of confidentiality we uphold.
West Coast Research complies fully with the Health Insurance Portability and Accountability Act (HIPAA). All protected health information you provide is handled securely and confidentially using administrative, physical, and technical safeguards to prevent unauthorized access or disclosure.
You have the right to access your personal data, request corrections, or withdraw consent at any time.