Are your clinical strategies keeping pace with the rapid evolution of renal drug development?
Renal drug development is entering a new era that demands deeper clinical insight and smarter design from day one. At Emerald Clinical Trials, we believe that early strategic input, not late-stage fixes, will define the next generation of kidney therapies.
Our new Renal Clinical Development Advisory Board is designed to help sponsors make smarter, faster, and more patient-centered decisions. Learn how top nephrologists and pharma veterans are reshaping clinical design, optimizing endpoints, and de-risking development from preclinical through commercialization. They offer real-world clinical insight grounded in day-to-day patient care, with a particular focus on IgA nephropathy, chronic kidney disease, and glomerular diseases.
Navigate Complexity with Expert Insight
Develop therapies that change lives worldwide. Our Renal Clinical Development Advisory Board helps chart your path to approval.
Through in-depth assessment of early-stage and ongoing clinical initiatives, you can fully realize your program’s scientific, regulatory, and commercial potential.
Working as an extension of your team, we help define clinical pathways that align with evolving standards of care, regulatory expectations, and real-world patient needs. From Phase I through pivotal trials, we guide critical decisions that accelerate renal drug development.
Our Renal Advisory Board—featuring world-renowned nephrologists Professor Jonathan Barratt, Professor David Wheeler, Dr. Richard Lafayette, and Dr. Adrian Liew, along with pharmaceutical development veteran Dr. Colin Orford—provides strategic clarity and insight across the entire drug development lifecycle. In addition, renal experts (90+) in the US, Europe, APAC, and LATAM are available to help sponsors design smarter studies from preclinical through pivotal phases.
Focused, efficient, and optimized for long-term success, our Renal Advisory Board helps you bring therapies to the patients who need them most.
Read Our Latest Article from CEO Mary Gunn, PhD, MBA, MA, LLM
Reimagining Renal Drug Development: Through Strategic Design
Renal drug development is going through a renaissance of sorts as the pace of innovation has accelerated rapidly in the past few years. Competitive pipelines are reshaping standards of care. Emerging biomarkers promise more precise endpoints. Yet for all this scientific momentum, the development pathway remains fraught with clinical, regulatory, and commercial risk.
That’s why we’ve launched a new Renal Clinical Development Advisory Board to address a critical gap we see in the ecosystem: the lack of integrated, domain-specific strategic design support for sponsors developing renal therapeutics.
Read the full article
Your Premier Renal Drug Development Partner
Contact Us to Find Out How We Can Help Shape Your Clinical Design
Why Emerald Clinical?
We help shape your development strategy to deliver clinical, regulatory, and commercial success.
Strategic Design Matters
Turn innovation into therapies with insight, experience, and trusted guidance from our Renal Advisory Board and 90+ nephrology KOLs.
Global Regulatory Intelligence
Navigate complex global requirements with in-country specialists who align your strategy with regional regulations and standards of care.
Real-World Relevance
Get nuanced perspectives on trial feasibility, endpoint selection, and emerging biomarkers based on the latest science and clinical practice.
See the Patient, Not Just the Protocol
Active clinical nephrologists design sustainable and scalable trials with a ground-level view of patient, provider, and payer demands.
Strategic Market Positioning
Drive clinical and commercial impact with competitive landscape analysis that informs clinical relevance and market success.
Competitive Intelligence = Smarter Strategy
Team up with experts who consult, guide, and execute, working closely with you from trial design and feasibility to submission.
“What we have is a global network of nephrologists who have delivered clinical trials and want to deliver more—and they know how to do it. Seeing these studies published in high-profile publications and new drugs getting approved for our patients justifies all the time and effort spent in delivering these clinical trials, and really changes clinical practice for the better.”
Professor Jonathan Barratt, PhD, FRCP
Meet the Experts Leading the Way
We’ve brought together industry-leading voices to shape the next generation of kidney care.

Colin Orford PhD, BSc
Colin Orford is a senior leader and experienced drug developer with 33 years of experience across GSK, Novartis, Quintiles, Eisai, and ICON. He combines scientific strategy with operational execution and is well-networked across biotech, pharma, and the pharmaceutical investment community. With 22 years of hands-on pharmaceutical development experience and 10 years leading ICON’s Drug Development team, Colin has spearheaded R&D project teams from preclinical through Phase IIIb, transitioning numerous molecules from candidate selection to late phase development. He has deep expertise in neurosciences, particularly in depression, anxiety, Alzheimer’s, and sleep disorders. Colin brings strong knowledge of regulatory guidelines for US, EU, and Japan markets, and expertise in due diligence for asset acquisition and investment funding. He has successfully guided Phase III teams through NDA and MAA submissions and works with emerging modalities such as cell and gene therapy.

Jonathan Barratt PhD, FRCP
Professor Barratt’s research is focused on a bench to bedside approach to improving understanding of the pathogenesis of IgAN. He is the IgAN Rare Disease Group lead for the UK National Registry of Rare Kidney Diseases and a Convener of the International IgAN Network. He is Chief Investigator for multiple international randomized controlled IgAN clinical trials and was a member of the FDA and American Society of Nephrology Kidney Health Initiative: Identifying Surrogate Endpoints for Clinical Trials in IgAN Work group. He is an Editorial Board member for Kidney International and the Journals of the American Society of Nephrology and is co-Chair of the UK Glomerulonephritis Clinical Study Group.

Professor David Wheeler MB, ChB, MD, FRCP
Professor Wheeler’s research focuses on the management of CKD. He is Professor of Kidney Medicine, University College London and Honorary Consultant Nephrologist, the Royal Free Hospital. He has participated in the development and running of several large-scale clinical trials testing therapeutic interventions in kidney disease. He has developed clinical practice guidelines for several organizations, most recently KDIGO, of which he has served as Co-Chair. He has completed a term as Chair of the International Society of Nephrology Advancing Clinical Trials Committee and is Deputy Chair of the ISN’s Western Europe Regional Board. He is currently England’s National Institute for Health Research National Specialty Lead for Renal disorders.

Dr. Richard Lafayette MD, FACP
Dr. Lafayette’s research interests include glomerular disease with a focus on IgA nephropathy. He is Professor of Medicine (Nephrology) at the Stanford University Medical Center and founder and director of the Stanford Glomerular Disease Center and its fellowship training program. His longstanding focus on IgA nephropathy has led to many evaluations and some elucidation of the pathogenesis of IgA nephritis and leadership in many clinical trials. He has more than 30 years of clinical experience and remains passionate in efforts to discover safer and more effective treatments.

Dr. Adrian Liew MD, MBBS, MRCP (UK), FAMS, FASN, FRCP, MClinEpid
Dr. Liew focuses on glomerular diseases, peritoneal dialysis, kidney transplantation, and diabetic kidney disease. He is Senior Consultant Nephrologist and Director of The Kidney & Transplant Practice at the Mount Elizabeth Novena Hospital, Singapore; the current elected secretary and executive of the International Society for Peritoneal Dialysis; current member of the executive committee for the KDIGO organization; and Deputy Chair of the Continuing Medical Education Committee for the ISN. A global Scientific Leader with roots in APAC, he is the only Singaporean appointed to the KDIGO working groups on Diabetes Management in Chronic Kidney Disease, and Update on Glomerular Diseases.
Together, they bring a uniquely integrated lens to every phase of development—from preclinical strategy to Phase III trial optimization.
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The future of renal drug development belongs to those who design smarter from day one. Planning your next program? Don’t go it alone.