active enzyme is not present in sufficient
quantities, Phe accumulates to abnormally high levels in the blood and
becomes toxic to the brain, resulting in a variety of complications
including severe mental retardation and brain damage, mental illness,
seizures, tremors, and limited cognitive ability. As a result of newborn
screening efforts implemented in the 1960s and early 1970s, virtually all
PKU patients under the age of 40 in developed countries have been diagnosed
at birth. Currently, PKU can only be managed by a Phe-restricted diet,
which is supplemented by nutritional replacement products, like formulas
and specially-manufactured foods; however, the strict diet is difficult for
most patients to adhere to the extent needed for achieving adequate control
of blood Phe levels. To learn more about PKU, please visit
http://www.PKU.com. Information on this website is not incorporated by
reference into this press release.
About BioMarin
BioMarin develops and commercializes innovative biopharmaceuticals for
serious diseases and medical conditions. The company's product portfolio
comprises two approved products and multiple clinical and preclinical
product candidates. Approved products include Naglazyme(R) (galsulfase) for
mucopolysaccharidosis VI (MPS VI), a product wholly developed and
commercialized by BioMarin, and Aldurazyme(R) (laronidase) for
mucopolysaccharidosis I (MPS I), a product which BioMarin developed through
a 50/50 joint venture with Genzyme Corporation. Investigational product
candidates include Kuvan(TM) (sapropterin dihydrochloride), a Phase 3
product candidate for the treatment of phenylketonuria (PKU), and 6R-BH4
for cardiovascular indications, which is currently in Phase 2 clinical
development for the treatment of peripheral arterial disease and sickle
cell disease. Both products are being developed in partnership with Merck
Serono, a division of Merck KgA of Darmstadt, Germany. For add
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SOURCE BioMarin Pharmaceutical Inc. Copyright©2007 PR Newswire. All rights reserved | |
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