NIH News Release
National Center for Research Resources

Tuesday, November 6, 2001

Kathy Kaplan
NCRR Information Officer
(301) 435-0888

New Resources to Assist with Gene Transfer Clinical Studies

Bethesda, Md. — The National Center for Research Resources (NCRR), a part of the National Institutes of Health (NIH), announced today the award of cooperative agreements in the amount of $2.65 million to establish National Gene Vector Laboratories (NGVLs) at five locations:

In gene transfer clinical studies, a vector serves as the vehicle to deliver a healthy gene to a part of the patient's body. This allows the correction of a genetic disorder or alteration of the properties of the cell. In this manner, gene transfer protocols, using several viral and non-viral vectors, have addressed such diseases as cystic fibrosis, severe combined immune deficiencies, hemophilia, cancer, heart disease, and AIDS.

"While the potential for gene transfer is great, the technical requirements and the expense of vector development, production, and safety testing often limits the capacity of investigators to proceed with their research," said Dr. Judith Vaitukaitis, NCRR Director. "A cooperative national effort will help move this promising research forward."

Frequently, physician scientists have had neither the ability to generate clinical grade vector in sufficient quantity nor the financial resources or time required to obtain the needed vector from commercial manufacturers. The limited availability of clinical quality vector constituted a barrier to progress in the field of gene transfer.

NCRR established a NGVL network in 1995 to help clinical researchers obtain adequate quantities of clinical-grade vectors. With today's announcement, the NGVLs will have not only the capability to produce and distribute a variety of human gene vectors, but also the capacity to provide toxicology studies at no cost to investigators for Phase I and Phase II human gene transfer clinical trials.

Toxicology data are frequently required by the Food and Drug Administration to minimize the likelihood of adverse events occurring during clinical research. This aspect of the NIH support is critical since many investigators' project grants do not provide funds for such studies. Since toxicology data are frequently considered proprietary and, therefore, not shared, toxicology studies are often repeated at great cost to the research community and funding entities. These new awards will help to eliminate these problems.

The responsibilities of the NGVLs:

Seven other NIH components will participate in the NGVL cooperative agreements, in addition to NCRR. They are: the National Cancer Institute; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Neurological Disorders and Stroke; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Dental and Craniofacial Research; National Institute of Allergy and Infectious Disease; and the National Institute of Child Health and Human Development.

NCRR is the nation's leading Federal sponsor of resources that enable advances in many areas of biomedical research. NCRR support provides the scientific research community with access to a diverse array of biomedical research technologies, instrumentation, specialized basic and clinical research facilities, mammalian and non-mammalian animal models, genetic stocks, and biomaterials such as cell lines, tissues, and organs.

The National Center for Research Resources is a component of the National Institutes of Health, U.S. Department of Health and Human Services.