- Big pharmaceuticals spent $49.5B on R&D in 2011
The Pharmaceutical Research and Manufacturers of America said 28 members invested $49.5 billion in research and development last year, about $100 million less than in 2010. Despite the drop, drugs undergoing clinical study or FDA review increased from 2,400 in 2005 to more than 3,200. Also, the FDA approved more than 30 drugs last year, compared with 22 in 2010. The Wall Street Journal/Dow Jones Newswires
(4/12)
 | Boehringer Ingelheim is the leading biopharmaceutical contract manufacturer with 35 years of experience – and 19 commercial products. At our globally licensed facilities in Biberach (Germany), Vienna (Austria) and Fremont (USA) we offer our customers flexible modules covering the entire process chain from cell line development to fill & finish. |
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- Agennix taps Lonza to produce talactoferrin
Lonza agreed to commercially manufacture Agennix's talactoferrin, an oral dendritic-cell-mediated immunotherapy in late-stage trials as a therapy for nonsmall-cell lung cancer, at its microbial production plant in Kourim, Czech Republic. The deal initiates the process required for Lonza to be approved as a producer of talactoferrin. Genetic Engineering & Biotechnology News
(4/12)
- Scientists: Drugmakers should release complete trial data
Drugmakers in the U.S. are not required to release full clinical trial reports to researchers or the public, and the FDA does not disclose the data that regulators review in the drug approval process, write research fellow Peter Doshi and epidemiologist Tom Jefferson. The European Medicines Agency intends to release clinical study data after regulators review a manufacturer’s application, and the FDA should follow suit, the scientists write. The New York Times (tiered subscription model)
(4/10)
- Old drugs give new hope to patients with rare diseases
Some drugs developed and tested to treat one disease show promise as therapy for another, sometimes rare, disease, NIH Director Francis Collins said at the TEDMED annual conference. For example, farnesyltransferase inhibitors used to treat cancer might mask the genetic mutation associated with progeria, which causes the body to age unnaturally quickly. Finding multiple uses for drugs is a win for drugmakers and the public, Collins said. ABC News/Medical Unit blog
(4/11), MedCityNews.com
(4/11)
| Company & Financial News |  |  |
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- Shire buys Pervasis for up to $200M
Shire has purchased Massachusetts-based biotech firm Pervasis Therapeutics in a deal reportedly worth "single-digit millions" at the start and up to $200 million after milestone fees are paid. The agreement
allows Shire to add Pervasis' endothelial cell technology to its regenerative medicine unit. Pervasis' experimental drug PVS-10200, a possible therapy for peripheral arterial disease, complements Shire's Dermagraft product for diabetic foot ulcers. American City Business Journals/Boston
(4/12), Fox Business/Dow Jones Newswires
(4/12)
- South Korea to invest $29M in stem cell research this year
The South Korean government will raise its investment in stem cell research and regenerative medical treatment to $29 million this year, four times higher than last year, according to the Ministry of Health and Welfare. The additional money will go in part to practical research and development to confirm the efficacy and safety of stem cell therapies. The Korea Times (Seoul)
(4/12)
| Food & Agriculture |  |  |
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- EFSA: Monsanto biotech maize safe for humans and the environment
Based on data from the 2010 farming season, a European Food Safety Authority panel concluded that cultivation of Monsanto's MON810 biotech maize poses no risks to human and animal health or the environment. The panel's scientific opinion, which appeared in the Post-Market Environmental Monitoring report for 2010, supported the findings of the agency's earlier evaluation of MON810 using 2009 data. FoodNavigator
(4/12)
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