Food and Drug
Administration
U.S. Department of Health and Human Services
Public Health Service 5600 Fishers Lane Rockville,MD 20857
FDA Talk Papers
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T97-64 Lenore Gelb:
301-827-6242
Dec 17, 1997 Broadcast Media: 301-827-3434 Consumer Inquiries: 800-532-4440
NEW BIOTECH PRODUCT FOR DIABETIC ULCERS
FDA has approved the first biotechnology product to treat deep diabetic foot and
leg ulcers.This product,becaplermin,is produced through recombinant DNA
technology and when combined with standard care, can improve the likelihood of
complete healing.
About 16 million people in the United States have diabetes and approximately 15
percent develop chronic ulcers of the foot and leg.Patients with diabetic ulcers
are at higher risk for local and systemic infections and amputation.
A majority of diabetic ulcers are quite deep and also have an adequate blood
supply. Becaplermin is approved to treat these ulcers,but is not currently
indicated for other ulcers,such as those caused by pressure.
Becaplermin must be used as a topical treatment, along with the surgical removal
of infected and dead tissue,daily cleanings,the strict avoidance of
weight-bearing activities and other standard measures for ulcer management.
The active ingredient in becaplermin is platelet derived growth
factor(PDGF).This growth factor,normally found in the blood, is produced in the
lab by inserting a gene into yeast. It works by recruiting and promoting cell
growth that helps to heal the ulcer.
Clinical studies of the product indicate that the likelihood of complete ulcer
closure, after up to 20 weeks of treatment, is greater when becaplermin is
used.Typical problems associated with ulcers were not increased,although 2
percent of the patients using becaplermin or the placebo gel had rashes.
The efficacy of becaplermin for non-diabetic ulcers is currently being evaluated
by its sponsor, R.W. Johnson Pharmaceutical Research Institute,Raritan, N. J. It
will be marketed under the trade name Regranex Gel by Ortho-McNeil
Pharmaceutical,Raritan, N.J.
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