Clinical Trials

Our Commitment to Discovery

Advancing liver and metabolic health requires innovation and patients are at the center of every breakthrough. Texas Liver Care collaborates with experienced research organizations, including Evidentis Clinical Research, to connect eligible participants with cutting-edge clinical trials in liver and metabolic diseases.

 

Our goal is to expand access to promising options today while helping shape tomorrow’s treatments through safe, ethical, and transparent research partnerships.

About Clinical Trials

Clinical trials study new therapies to determine whether they are safe, effective, and beneficial for patients. Each phase of research serves a distinct purpose:

Phase 1 – Safety & Dosing

Determines how a new treatment behaves in the body and identifies a safe dosage range. These studies are often conducted in healthy volunteers (First-in-Human) but may also involve individuals with liver or metabolic diseases when direct safety data are needed.

Phase 2 – Effectiveness & Refined Safety

Evaluates the treatment’s effectiveness in a small group of patients while continuing to monitor safety.

Phase 3 – Confirmation & Comparison

Confirms the treatment’s benefits in larger populations, compares it with existing standard therapies, and tracks side effects to support FDA approval.

Phase 4 – Post-Approval & Long-Term Monitoring

Conducted after FDA approval to assess long-term outcomes, performance in real-world use, and ongoing safety.

Why Participate?

Patients who join research studies help advance medical progress and may personally benefit from:

Early Access: Opportunity to receive promising investigational therapies under expert supervision.

Comprehensive Oversight: Frequent assessments and close safety monitoring by experienced clinical professionals.

Contribution to Progress: Participation supports discovery of new treatments for liver and metabolic diseases.

Compensation and Support: Some studies provide payment for time and travel, as described in each consent form.

What to Expect

Before joining a study, you will complete a brief pre-screening to confirm eligibility. The study team will provide a clear explanation of all procedures, potential risks, and your rights before you decide whether to participate (informed consent).

Most trials involve:

Regular study visits for treatment or assessments

Safety labs, imaging, and health monitoring

Assistance with travel and scheduling when available

How to Get Involved

Patients interested in clinical research can join the Clinical Trial Registry to receive updates about upcoming studies that may match their health profile. Participation in the registry is voluntary and does not automatically enroll you in any study.

Privacy & Data Use: Your information will be stored securely and used only to contact you about research opportunities through Evidentis™. We do not sell or share personal data for marketing purposes. You may opt out at any time.

Learn More

For details on currently enrolling studies, investigator services, and research infrastructure, visit our collaborating research site: Evidentis Clinical Research

Request a Call About Clinical Trials