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(682) 651-1112
We conduct clinical trials in liver, metabolic, and cardiometabolic conditions. Our studies evaluate emerging therapies and aim to advance treatment options for patients. Participation is free, and eligible participants may receive compensation for study-related time and travel, depending on the study.
We are actively conducting and preparing clinical studies in the following areas:
Metabolic Dysfunction-Associated Steatohepatitis (MASH)
Alcohol-Associated Liver Disease (ALD)
Cholestatic Liver Diseases (e.g., PBC, PSC)
Cirrhosis and Complications of Advanced Liver Disease
Obesity and Cardiometabolic Conditions
Specific study availability changes over time. Eligibility depends on individual study criteria.
All information provided is kept confidential and used solely for clinical trial screening and research purposes.
Evidentis uses a short eligibility form to identify which clinical trials may be a good match based on your health history and interests. If no current study is appropriate, your information remains securely stored so we can contact you about future opportunities.
The Evidentis clinical trial registry allows us to notify individuals about current and future studies that may be a good fit based on health history and research interests. Joining the registry does not obligate you to participate in any study.
What to expect when taking part in a clinical trial at Evidentis.
Clinical trials follow a protocol-defined process designed to evaluate investigational therapies in a safe and organized manner. While individual studies vary, participants who proceed beyond initial screening can generally expect the steps below.
Start by filling out our short online form. This helps determine whether you may be a match for a current study or future opportunities.
If your information suggests a possible match, a member of our team will reach out to review details, answer questions and discuss next steps.
Most studies require one or more screening visits to confirm eligibility. These may include questionnaires, physical measurements, laboratory testing, imaging, or other evaluations required by the study protocol.
Participants who meet eligibility criteria take part in scheduled study visits. Depending on the protocol, visits may include clinic appointments, laboratory assessments, imaging, questionnaires, or time-specific procedures.
Some studies include follow-up visits after completion of the main study period to monitor outcomes and collect additional study data over time.
Healthcare providers may refer eligible patients to Evidentis clinical trials through a secure, HIPAA-compliant process that supports continuity of care and appropriate follow-up.
How to Refer:
Submit the secure referral form with relevant clinical details.
Our team reviews study availability and eligibility criteria.
We will contact the patient directly and provide updates when appropriate and permitted.
Please share patient details for clinical trial referral.