| Ceftobiprole’s Non-Approval in the U.S. Changes the Forecast for MRSA and Community-Acquired Pneumonia – Who Will Get the Projected $150 Million?
Based on our Pharmacor advisory services entitled Methicillin-Resistant Staphylococcus aureus (MRSA) and Community-Acquired Pneumonia, Decision Resources is offering an exclusive Pharmacor analyst call entitled Ceftobiprole’s Non-Approval in the U.S. Changes the Forecast for MRSA and Community-Acquired Pneumonia – Who Will Get the Projected $150 Million? Because this presentation will feature major updates, it is ONLY available to purchasers of one or both of these Pharmacor advisory services.
Please contact us to learn how you can purchase one or both of these Pharmacor advisory services and attend the analyst call.
The recently-announced rejection by the U.S. Food and Drug Administration (FDA) of Johnson & Johnson/Basilea’s application to market ceftobiprole for the treatment of complicated skin and skin structure infections will create a significant void in the MRSA pipeline. As a result of the FDA’s action, Decision Resources has updated its Pharmacor Methicillin-Resistant Staphylococcus aureus (MRSA) and Community-Acquired Pneumonia advisory services. Ceftobiprole, which was widely considered to be a highly promising drug candidate, had been previously forecasted by Decision Resources to garner more than $150 million in peak year sales for the treatment of MRSA and community-acquired pneumonia in the world’s major pharmaceutical markets.
This 15-minute analyst call, presented by Director of Infectious Diseases Danielle Drayton, Ph.D., will answer the following questions:
- How will the market absence of ceftobiprole affect the uptake of current and emerging therapies for MRSA and community-acquired pneumonia, most notably Forest/Novexel/Takeda’s ceftaroline? Which agents will fill the void created by ceftobiprole’s absence?
- What is Decision Resources’ updated forecast for the MRSA and community-acquired pneumonia drug markets?
- Through 2018, what effect will ceftobiprole’s non-approval and significantly delayed market entry have on the overall infectious diseases drug market?
Dr. Drayton will conduct a live Q & A session after the presentation.
Registration
Ceftobiprole’s Non-Approval in the U.S. Changes the Forecast for MRSA and Community-Acquired Pneumonia – Who Will Get the Projected $150 Million?
January 14, 2010 at 10 a.m. U.S. Eastern Time, 4 p.m. Central European Time (Paris).
To learn how you can purchase one or both of these Pharmacor advisory services and attend the analyst call, please contact us using the information below.
Contact Us
In North America — Keith Rourke at 781-296-2656 or krourke@dresources.com
In Europe — Kaj van Langendonck at +32-2-357-06-14 or kvanlangendonck@decisionresources.be
In Japan — Makiko Yoshimoto at +81-3-5401-2615 or makiko@dresources.jp |
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Date & Time
Thursday, January 14, 2010
10 a.m. U.S. Eastern Time, 4 p.m. Central European Time Duration
15 minutes  |
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Danielle Drayton, Ph.D. is the Director of Infectious Diseases at Decision Resources. Prior to joining the company, she completed a postdoctoral fellowship at CBR Institute for Biomedical Research (Harvard Medical School), where she investigated a novel role of natural killer cells in adaptive immunity. She has conducted extensive research on the mechanisms of tumor necrosis factor- and lymphotoxin-mediated lymphoid organ development, inflammation, and angiogenesis and has coauthored numerous peer-reviewed research articles in these areas. Dr. Drayton holds a Ph.D. in immunobiology from Yale University and a B.S. in microbiology and immunology from the University of Miami, Florida. |
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