UpcomingVirtual

2026 FDA Cellular, Tissue, and Gene Therapies Advisory Committee Meeting

by FDA

The 2026 FDA Cellular, Tissue, and Gene Therapies Advisory Committee Meeting is a pivotal event organized by the U.S. Food and Drug Administration (FDA). This committee is dedicated to reviewing and evaluating data concerning the safety, effectiveness, and appropriate use of human cells, tissues, gene transfer therapies, and xenotransplantation products intended for transplantation, implantation, infusion, and transfer in the prevention and treatment of a broad spectrum of human diseases, as well as in the reconstruction, repair, or replacement of tissues for various conditions.

The meeting will cover key topics such as the latest advancements in cellular therapies, tissue transplantation, gene transfer therapies, and xenotransplantation. Discussions will focus on evaluating new research findings, assessing clinical trial data, and considering regulatory pathways for emerging therapies. The agenda will also include deliberations on the ethical implications and safety concerns associated with these innovative treatments.

Attendees will have opportunities to engage in networking sessions, participate in panel discussions, and attend presentations by leading experts in the field. The event will feature an expo hall showcasing the latest technologies and products related to cellular, tissue, and gene therapies. Notable speakers will include prominent researchers, clinicians, and regulatory officials who will share their insights and experiences.

This meeting is essential for healthcare professionals, researchers, industry representatives, and policymakers involved in the development, regulation, and application of cellular, tissue, and gene therapies. Participation will provide valuable insights into current trends, regulatory considerations, and future directions in these rapidly evolving fields.

Speakers(18)

Alexis C. Komor, Ph.D.

Assistant Professor at University of California, San Diego

Dr. Komor is an Assistant Professor at UC San Diego, specializing in gene editing.

Amy Shapiro, M.D.

Medical Director and CEO at Indiana Hemophilia & Thrombosis Center

Dr. Shapiro is the Medical Director at the Indiana Hemophilia & Thrombosis Center, specializing in sickle cell disease.

Christopher K. Breuer, M.D.

Director of Tissue Engineering Program and Surgical Research at Nationwide Children’s Hospital

Dr. Breuer leads the Tissue Engineering Program and Surgical Research at Nationwide Children’s Hospital, focusing on pediatric surgery.

Donald B. Kohn, M.D.

Distinguished Professor at University of California, Los Angeles

Dr. Kohn is a Distinguished Professor at UCLA, specializing in gene therapies for blood diseases.

Eric Crombez, M.D.

Chief Medical Officer at Ultragenyx Gene Therapy

Dr. Crombez serves as the Chief Medical Officer at Ultragenyx Gene Therapy, representing industry perspectives.

Gil I. Wolfe, M.D.

Professor and Chairman of Neurology at University at Buffalo/SUNY

Dr. Wolfe is the Professor and Chairman of Neurology at the University at Buffalo, specializing in neurology.

Jasmine Hightower, M.S.W.

Patient Representative

Ms. Hightower serves as a patient representative, providing insights on sickle cell disease.

John F. Tisdale, M.D.

Branch Chief

Dr. Tisdale serves as Branch Chief, focusing on stem cell research.

Joseph Wu, M.D., Ph.D.

Director, Stanford Cardiovascular Institute at Stanford University

Dr. Wu directs the Stanford Cardiovascular Institute, with expertise in cardiology and radiology.

Kathleen O’Sullivan-Fortin, Esq.

Founder at ALD Connect, Inc.

Ms. O’Sullivan-Fortin is the founder of ALD Connect, Inc., serving as the consumer representative.

Event Details

Date
October 31, 2026
Location
🇺🇸 United States
Audience
Healthcare professionals, researchers, industry representatives, policymakers
In 18 weeks

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