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- J&J's tuberculosis drug gets FDA panel support
An FDA panel has backed the safety and efficacy of Johnson & Johnson's bedaquiline drug for tuberculosis, but also pointed out possible heart and liver-safety issues. The drug works by targeting the adenosine triphosphate synthase enzyme, which the pathogen requires to generate energy. Reuters
(11/28)
- AesRx reports promising data for sickle cell disease drug
AesRx said data from a Phase I study of its sickle cell disease treatment Aes-103 showed the drug is safe and well-tolerated by patients. The data are set to be presented at a hematology meeting. Following the positive findings, AesRx has started a second trial at the NIH Clinical Center in Bethesda, Md., that will involve patients with sickle cell disease. Mass High Tech (Boston)
(11/27)
- Method allows aging stem cells to rejuvenate
Canadian researchers have developed a method to prompt aging stem cells to rejuvenate. The researchers created a "micro-environment" conducive to growing heart tissue from stem cells collected from elderly patients. The discovery could allow for the development of "young" patches for treating or healing damaged or diseased hearts without the fear of rejection. ZeeNews.com (India)/Indo-Asian News Service
(11/28)
| Company & Financial News |  |  |
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- Panacela lands $4.6M contract to develop infectious disease drugs
The Ministry of Industry and Trade of the Russian Federation awarded Panacela Labs a contract worth around $4.6 million to develop Xenomycins, a family of anti-infective compounds that works by targeting pathogenic microbe DNA. In preclinical studies, Xenomycins showed efficacy against parasites and pathogenic fungi that cause candidiasis, aspergillosis and other infections. "We expect that the contract will enable us to accelerate our preclinical program and evaluate the potential application of Xenomycins against life threatening infectious diseases," Panacela CEO Dmitry Tyomkin said. Genetic Engineering & Biotechnology News
(11/27)
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| Food & Agriculture |  |  |
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- Study linking biotech corn to cancer has serious defects, EFSA says
There is no need to re-assess the safety of Monsanto's biotech corn NK603 because the study that linked the crop to cancer risks in rats had major design and methodology flaws, according to the European Food Safety Authority. "Conclusions cannot be regarded as scientifically sound because of inadequacies in the design, reporting and analysis of the study as outlined in the paper," EFSA said. The Wall Street Journal
(11/28)
| Industrial & Environmental |  |  |
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- Poll: Advanced biofuel execs believe federal support will stay
Most of the participants in last month's Advanced Biofuels Markets conference in San Francisco were optimistic that federal support for biofuels would be continued or increased in 2013, and that commercial-scale cellulosic ethanol production would be achieved next year, a survey showed. More than 67% of respondents believed that the Renewable Fuel Standard would stay in its current form through 2013, the poll showed. BiofuelsDigest.com
(11/28)
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