News Breaks |
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| March 14, 2013 |
| 06:54 EDT |  | LLY, RHHBY | FDA wants to relax criteria for Alzheimer's drug approval, NY Times says The FDA intends to make it easier for companies to obtain approval of new treatments for Alzheimer’s disease, according to The New York Times. Under the agency's proposal, drugs could be approved if they improve peoples' performance on cognitive tests even before symptoms become apparent, and companies would not have to demonstrate that their drugs improve patients' functioning, the newspaper explained. Currently companies must show that their drugs improve patients' day to day functioning in order to obtain FDA approval of treatments, The Times added. Reference Link |
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News For LLY;RHHBY From The Last 14 Days Check below for free stories on LLY;RHHBY the last two weeks. |
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| May 23, 2013 |
| 15:19 EDT |  | RHHBY | FDA announces approval of Roche diabetes test
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| May 22, 2013 |
| 10:33 EDT |  | RHHBY | Bristol-Myers jumps after Citi ups rating on cancer potential
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| 10:00 EDT |  | RHHBY | On The Fly: Analyst Upgrade Summary
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| 06:02 EDT |  | RHHBY | Roche upgraded to Buy from Neutral at Citigroup
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| May 21, 2013 |
| 20:03 EDT |  | RHHBY | Roche, Sigma-Aldrich teamed for Life bid, Reuters says
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| 07:24 EDT |  | LLY | Global Health Care to host a conference
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| May 20, 2013 |
| 17:26 EDT |  | RHHBY | Regeneron, Genentech, Sanofi enter into 'Zaltrap agreement'
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| 17:20 EDT |  | RHHBY | Regeneron,, Bayer, Genentech resolve certain patent disputes
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| May 16, 2013 |
| 08:55 EDT |  | LLY | BofA/Merrill's pharmaceuticals analysts hold analyst/industry conference call
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| May 15, 2013 |
| 15:59 EDT |  | RHHBY | Roche exploring sale of blood glucose meters unit, Reuters says
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| 12:13 EDT |  | RHHBY | Roche management to meet with Jefferies Meeting to be held in London on May 17 hosted by Jefferies. |
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| 11:38 EDT |  | RHHBY | Roche says FDA approves Tarceva tablets for specific lung cancer situation
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| May 14, 2013 |
| 16:55 EDT |  | RHHBY | FDA approves Roche's cobas EGFR mutation test with Tarceva
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| 09:09 EDT |  | LLY | Eli Lilly announces CEO John Lechleiter recovering from surgery
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| 07:24 EDT |  | LLY | EBD Group to host a conference BioTrinity 2013 is being held in Newbury, England on May 14-16. |
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| May 13, 2013 |
| 08:55 EDT |  | RHHBY | Biosimiliar drug bill to be taken up in Senate, LA Times reports
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| 07:30 EDT |  | RHHBY | TechConnect to host a summit 2013 National Innovation Summit is being held in Washington, D.C. on May 12-16. |
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| May 10, 2013 |
| 15:59 EDT |  | RHHBY | Roche spokesman reiterates that Illumina is "off the table," Bloomberg reports
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| 11:48 EDT |  | RHHBY, LLY | Drugmakers to face pressure on U.S. prices, Reuters says
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| 08:02 EDT |  | LLY | Eli Lilly's Enzastaurin Phase III study did not meet primary endpoint Eli Lilly announced Phase III clinical trial results from enzastaurin's PRELUDE study, which explored the molecule as a monotherapy in the prevention of relapse in patients with diffuse large B-cell lymphoma. The study failed to show a statistically significant increase compared to placebo in disease-free survival in patients at high risk of relapse following rituximab-based chemotherapy. There were no new safety findings, and the safety data were consistent with previously disclosed studies. Lilly will stop development of enzastaurin, which is expected to result in a second-quarter charge to R&D expense of approximately $30M. The company's previously-issued financial guidance for 2013 remains unchanged. |
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