Discover Opportunities in Rheumatology Clinical Trials

Find support for your rheumatology clinical trial journey

Across rheumatology, clinical trials are driving innovation for people who need more than standard treatments. Our team can help you understand your options and guide you through each step. Explore the conditions below or connect with our team for guidance if you're unsure where to start.

Our rheumatology trials cover:

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Frequently Asked Questions

A clinical trial is a research study that evaluates how a new medical approach — such as a medication, device, vaccine, or treatment strategy — works in people. Trials help determine whether new options are safe and effective for broader use.

Participants often consider clinical trials to:
  • Learn about potential new treatment options
  • Receive study-related care and monitoring
  • Be part of medical innovation that may help others
  • Receive reimbursement for time and travel (varies by study)

All clinical trials involve potential risks and benefits, which vary by study. Before you decide whether to participate, you’ll go through a thorough informed consent process where you’ll learn about:

  • The study’s purpose
  • What participation involves
  • Possible side effects or risks
  • Who to contact with questions

Each study is approved by an Institutional Review Board (IRB) or Research Ethics Board (REB) to ensure the rights and welfare of participants are protected. Studies are also regulated by:

  • The U.S. Food and Drug Administration (FDA)
  • Health Canada, the Canadian authority for health research
  • Local ethical and scientific review committees

No. Participation is always voluntary. You may leave a study at any time, for any reason, without penalty or loss of access to your regular care.

Some studies offer reimbursement for time, travel, or related expenses. Details vary by study and will be provided before you decide whether to take part.

Each study has specific eligibility criteria to ensure safety and valid results. If a study isn’t a fit, we can—with your permission—contact you about future opportunities.

It depends. Some studies may require changes to your current medications or care. You’ll be informed of any potential changes before you enroll. You can discuss this with our team — and with your regular doctor — before making a decision.

Yes. Centricity Research conducts clinical trials that are reviewed by independent ethics boards, follow national and international regulations, and adhere to Good Clinical Practice (GCP) standards. We’re committed to ethical conduct and patient-first research.

Yes. Our team is here to answer your questions and help you understand what participation would involve, without any pressure. We’ll make sure you have all the information you need to make the decision that’s right for you.

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