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Agilent Expands Therapeutic Nucleic Acids Manufacturing Capacity
Dow Nucleic Acids Medicines Business Assets Acquired
SANTA CLARA, Calif., May 7, 2008 -- Agilent Technologies Inc. (NYSE: A) today
announced the expansion of its nucleic acid active pharmaceutical ingredient
(API) manufacturing facility in Boulder, Colo. Agilent’s Nucleic Acids Solutions
Division is adding large-scale nucleic acid synthesis, purification and drying
capacity that will come on stream by the end of 2008. As a part of this
expansion, Agilent has purchased from Dowpharma all of the assets of its Nucleic
Acid Medicines business. The financial terms of the purchase were not disclosed.
This is the second manufacturing expansion for the Boulder, Colo., facility
since Agilent purchased the business in 2006.
“This expansion represents a significant commitment by Agilent to meet the
supply demands of a rapidly expanding market,” said James Powell, general
manager of Agilent’s Nucleic Acid Solutions Division. “Merging our expansion
plans with the acquisition of Dow’s assets will allow Agilent to respond to this
demand well ahead of our original plan. Agilent will have the ability to serve
customers from pre-clinical through large-scale commercial launch with
facilities, equipment and expertise across a broad range of nucleic acid APIs.”
Agilent’s capacity expansion features the addition of a 200-1,000 mmole
synthesizer capable of producing kilo quantities of API per synthesis batch.
Additional downstream processing capability will also be added with a 30 liter
per min chromatography system and two multikilo lyophilization units.
Corresponding infrastructure and reaction vessels will be added for custom
conjugation chemistries and duplex annealing of siRNAs; addressing the fastest
growth segment of the oligonucleotide market.
To learn more, please visit Agilent at booth 514 at the TIDES Conference at Red
Rock Resort and Spa, Las Vegas, Nev., May 19-21.
About Agilent in Nucleic Acids
Agilent, through its Nucleic Acid Solutions Division, is a leading provider of
therapeutic nucleic acid development services and manufacturing solutions for
the biotech and pharmaceutical industries. The division operates a 33,500 square
foot cGMP nucleic acid API contract manufacturing facility in Boulder, Colo. The
state-of-the-art facility manufactures of a wide range of nucleic acid
therapeutics, including DNA, RNA, phosphorothioates, mixed PO/PSs, aptamers,
conjugated aptamers, siRNA and various modified RNAs. In addition to
manufacturing cGMP nucleic acid therapeutics, Agilent also offers an array of
turnkey services, including development of analytical methods and processes,
stability studies, quality control, and regulatory support. Information about
Agilent’s Nucleic Acid Solutions Division is available at
www.agilent.com/chem/nucleicacid .
About Agilent Technologies
Agilent Technologies Inc. (NYSE: A) is the world’s premier measurement company
and a technology leader in communications, electronics, life sciences and
chemical analysis. The company’s 19,000 employees serve customers in more than
110 countries. Agilent had net revenues of $5.4 billion in fiscal 2007.
Information about Agilent is available on the Web at
www.agilent.com .
# # #
NOTE TO EDITORS: Further technology, corporate citizenship and executive news is
available on the Agilent news site at
www.agilent.com/go/news
Press release URL:
http://www.agilent.com/about/newsroom/presrel/2008/07may-ca08030.html
Additional metadata keywords (for Web use only): therapeutic nucleic acids,
manufacturing, Dowpharma, API
Claudia Hachtel, Agilent Technologies
+49-7243-602 100
claudia_hachtel@agilent.com
Nicki Muir, Alto Marketing
+44-1489-55 76 72
nickim@alto-marketing.com
Sarah Perceval, Alto Marketing
+44-1489-55 76 72
sarahp@alto-marketing.com
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