AcceleratingBreakthroughs, with Trusted Research

We partner with sponsors to deliver rigorous, patient-centered clinical trials led by experts in liver and metabolic disease.

Your Clinical Research Partner

We conduct Phase I–IV clinical trials with a focus on quality, ethics, and efficiency for sponsors across therapeutic areas.

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Patient-Focused Care

Patients are the foundation of our work. We ensure each participant feels respected, informed, and cared for throughout the study journey.

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Operational Excellence

Our skilled team and optimized workflows ensure fast study start-up, precise data collection, and consistent regulatory compliance. Everything is delivered on time and aligned with your goals.

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Introducing

Dr. Adrian Di Bisceglie

Dr. Di Bisceglie brings over 40 years of clinical research experience in liver and metabolic diseases. A former AASLD President and internationally recognized hepatologist, he leads with deep scientific insight and a legacy of innovation in clinical trials.

Liver Disease Expertise

Over 40 years in liver and metabolic disease studies

Therapeutic Innovation Leader

Experience driving metabolic and liver drug development

Academic Excellence

Led SLU’s Hepatology department for over 20 years

Global Recognition

Former AASLD President & NIH/CDC/FDA advisor

We Are

KAD Clinical Research

We provide sponsors and CROs with full-service clinical trial execution across Phase I-IV studies, specializing in liver disease, metabolic disorders, and non-invasive diagnostics with rapid start-up and centralized regulatory support.

Prime Location for Patient Access

Our research site is physically embedded within the prominent Clayton Sleep Institute, the region’s premiere institution for the study of sleep disorders and the care of patients with sleep disorders.

Experienced Investigators & Integrated Site Management

Led by KOLs and supported by a cohesive on-site team ensuring operational continuity and oversight.

Rapid Study Start-Up & Contracting

Streamlined processes for budgets, feasibility, and regulatory startup to get trials moving fast.

Central IRB & Regulatory Compliance

Fully aligned with central IRB use and built-in SOPs for audit-ready compliance.

Patient Recruitment & Retention Excellence

Dedicated team using outreach, screening protocols, and retention strategies to hit enrollment goals.

On-Site Lab & Liver Diagnostics

Non-invasive testing capabilities and secure drug/lab storage support complex liver trials.

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