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Arrangements complementing current therapeutic areas
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Cholesterol (Schering-Plough)
Respiratory (Schering-Plough)
HIV (Cambridge Antibody Technology, Crucell, CytRx)
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Antibacterials (Elitra)
Osteoporosis (Celera)
Ophthalmics (Cole Eye Institute)
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Arrangements expanding into new, large therapeutic areas
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Diabetes (Kyorin)
Neuroscience (NeuroTargets)
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Influenza (Biodiem)
Hepatitis C (ISIS)
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Arrangements for cutting-edge research technologies
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Pharmacogenomics (Rosetta Inpharmatics7)
Genomics/Proteomics (DoubleTwist, LifeSpan, Amersham Pharmacia, Proteome)
Gene Tools/Targeting (Lexicon, Sangamo, Affymetrix)
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Lead Identification (NeoGenesis)
Assay Development (Chromagen)
Chemical Libraries (Array Biopharma, Chembridge, Discovery Partners)
Knock Out Mice (Deltagen, Lexicon)
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Arrangements for cutting-edge biologics and drug delivery technologies |
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Drug Delivery (Elan/Nanosystems, Flamel, Symyx)
Biologics (ProBioGen)
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4 Merck plans to submit an expanded New Drug Application
(NDA) for Arcoxia to the U.S. Food and Drug Administration
in order to include new efficacy data that will better position the
product to compete successfully in the coxib class, where there already
are three entrants. Accordingly, on March 13, 2002, Merck withdrew
the original U.S. NDA for the investigational medicine. Merck is submitting
the additional efficacy data to support a new indication for ankylosing
spondylitis, which is a chronic, inflammatory disorder primarily involving
the spine. Timing of the expanded submission has not been determined.
In addition to the indications listed above, Merck is seeking an indication
for acute gouty arthritis. The regulatory process for Arcoxia
outside the United States continues uninterrupted.
5 Scheduled for filing in 2002
6 Ezetimibe is under development around the globe (except in Japan) through
a joint venture between Merck and Schering-Plough Corporation
7 Purchased by Merck on July 19, 2001
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