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Date:  Dec. 5, 2013

 

FOR IMMEDIATE RELEASE:

 

In Most Cases, Human Gene Transfer Research No Longer Requires Additional Review by NIH Advisory Committee; Other Areas of Research on Humans May Benefit From This Type of Oversight

 

WASHINGTON -- In most cases, human gene transfer research is no longer novel or controversial enough to require additional review from the National Institutes of Health’s Recombinant DNA Advisory Committee, known as RAC, says a new report by the Institute of Medicine.  Patient safety is always paramount, the report says, but most individual RAC reviews no longer provide benefits beyond the existing regulatory and oversight framework and may be impeding scientific advancement with unnecessary administrative burdens.

 

However, NIH should consider developing a process – using RAC as a model – to rigorously review research on humans in any scientific realm that uses applications from emerging technologies or techniques that pose unknown or significant risks.

 

“The government’s role in research must be, first and foremost, to safeguard the rights, dignity, and health of human subjects, while also facilitating vital scientific research to prevent and treat major health threats,” said Lawrence O. Gostin, university professor at Georgetown University Law Center and chair of the committee that wrote the report. "The RAC has instilled public confidence in an area of research that was once deeply controversial, and the RAC model could serve as a method for transparent engagement and review of any novel scientific research that poses unknown or heightened risk.”

 

Human gene transfer research involves the introduction of genetic material into a human subject for diagnostic or therapeutic purposes.  Individual gene transfer research protocols – extensive written research plans -- currently must be reviewed by the U.S. Food and Drug Administration as well as by multiple oversight bodies at individual research institutions.  Each protocol for NIH-funded research is also reviewed by RAC, which then selects a small number of potentially controversial or novel research protocols for further oversight and public review. The RAC no longer directly regulates human gene transfer research but instead advises NIH on protocols and provides a public forum for discussing scientific, technical, and ethical considerations.

 

Since RAC was formed in the 1970s, decades of extensive clinical and research experience have helped alleviate many of the initial concerns about human gene transfer research.  Hundreds of clinical trials – predominantly Phase I clinical trials designed to evaluate safety – have been completed and much has been learned about how to ensure the safety of research participants.   In addition, the promise of more effective treatments for devastating and debilitating diseases has increased the public’s positive perceptions of this research.

 

RAC should only review individual research protocols in exceptional cases, the committee concluded. The report identifies specific criteria that a research protocol should meet before it is determined to require RAC review, such as when a new vector, genetic material, or delivery method is first used on human subjects, and when protocols cannot be adequately reviewed by other oversight and regulatory bodies.  The NIH director should consult with other regulatory and oversight authorities to determine whether RAC review is warranted.  But even if proposed research doesn’t meet these criteria, the director should have the flexibility to select research protocols for RAC review that may present significant societal or ethical concerns.

 

In addition to gene transfer, other emerging technologies to be used in human research, such as nanotechnology, could benefit from public discussion and oversight, the report says.  The NIH director should convene an ad hoc working group to consider whether providing oversight and a venue for public deliberation similar to RAC for research on humans involving other emerging applications is needed.  The report notes that such oversight and review should focus only on cases that have generated significant public concern or that fall outside existing regulatory capacities.

 

The study was sponsored by the National Institutes of Health.   Established in 1970 under the charter of the National Academy of Sciences, the Institute of Medicine provides independent, objective, evidence-based advice to policymakers, health professionals, the private sector, and the public.  The National Academy of Sciences, National Academy of Engineering, Institute of Medicine, and National Research Council make up the National Academies.   A committee roster follows.

 

Contacts:

Molly Galvin, Senior Media Relations Officer

Rachel Brody, Media Relations Associate

Office of News and Public Information

202-334-2138; e-mail news@nas.edu

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Additional resources:

Full Report
Report in Brief
___________________________________________________________________________________________
Copies of Oversight and Review of Clinical Gene Transfer Protocols: Assessing the Role of the Recombinant DNA Advisory Committee are available from the National Academies Press on the Internet at
http://www.nap.edu or by calling tel. 202-334-3313 or 1-800-624-6242.  Reporters may obtain a copy from the Office of News and Public Information (contacts listed above).

 

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INSTITUTE OF MEDICINE

Board on Health Sciences Policy

 

Committee on the Independent Review and Assessment of the Activities of the NIH Recombinant DNA Advisory Committee

 

Lawrence O. Gostin, J.D. (chair)

University Professor and the Linda and Timothy O'Neill Professor of Global Health Law

Georgetown University;

Professor of Public Health

Johns Hopkins University; and

Director

O'Neill Institute on National and Global Law, and

Director

WHO Collaborating Center on Public Health Law and Human Rights

Georgetown University Law Center

Washington, D.C.

 

Kenneth I. Berns, Ph.D., M.D.

Distinguished Professor

Department of Molecular Genetics and Microbiology

University of Florida College of Medicine

Gainesville

 

R. Alta Charo, J.D.

Warren P. Knowles Professor of Law and Bioethics
School of Law, and
Department of Medical History and Bioethics
School of Medicine and Public Health
University of Wisconsin

Madison

 

Howard J. Federoff, M.D., Ph.D.

Executive Vice President for Health Sciences
Department of Neurology, and

Executive Dean

Georgetown University School of Medicine

Washington, D.C.

 

Jeffrey P. Kahn, M.P.H., Ph.D.

Levi Professor of Bioethics and Public Policy

Berman Institute of Bioethics

Johns Hopkins University

Baltimore

 

Terry Magnuson, Ph.D.

Vice Dean for Research, and
Sarah Graham Kenan Professor and Chair

Department of Genetics

University of North Carolina

Chapel Hill

 

Joseph G. Perpich, M.D.

Principal and Senior Medical Adviser

JBS International Inc.

Bethesda, Md.

 

Sharon F. Terry

President and CEO

Genetic Alliance

Washington, D.C.

 

Inder M. Verma, M.Sc., Ph.D.

Professor

Laboratory of Genetics, and

American Cancer Society Professor of Molecular Biology and

Irwin and Joan Jacobs Chair in Exemplary Life Science

Salk Institute for Biological Studies

La Jolla, Calif.

 

John E. Wagner, M.D.

Professor of Pediatrics

University of Minnesota Medical School

Minneapolis

 

Daniel J. Wattendorf, M.D.

Deputy Chief

Medical Innovations, and
Program Manager

Defense Advanced Research Projects Agency

U.S. Department of the Air Force

Arlington, Va.

 

STAFF

 

Rebecca N. Koehler, Ph.D.

Study Director