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News Breaks
January 24, 2014
05:56 EDTCBLICleveland BioLabs downgraded to Perform from Outperform at Oppenheimer
Oppenheimer downgraded Cleveland BioLabs calling BARDA's decision to terminate negotiations for the continued development of Entolimod a significant setback.
News For CBLI From The Last 14 Days
Check below for free stories on CBLI the last two weeks.
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September 15, 2014
07:10 EDTCBLICleveland BioLabs announces approval to start CBLB612 Phase 1 study in Russia
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September 10, 2014
07:37 EDTCBLICleveland BioLabs announces extra 180 days to regain NASDAQ compliance
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September 8, 2014
07:06 EDTCBLICleveland BioLabs, Sabby announce resolution of litigation
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September 3, 2014
14:09 EDTCBLICleveland BioLabs up 41% in afternoon trading following FDA opinion on entolimod
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07:23 EDTCBLICleveland BioLabs to host conference call
Conference call to discuss update of July FDA meeting will be held on September 3 at 11 am. Webcast Link
07:06 EDTCBLICleveland BioLabs to submit pre-EUA application for entolimod
Cleveland BioLabs announced that the minutes from its meeting with the FDA in July confirmed that the company's existing efficacy and safety data and animal-to-human dose conversion are sufficient to proceed with a pre-Emergency Use Authorization, or pre-EUA, submission for entolimod for reducing the risk of death following exposure to potentially lethal irradiation occurring as the result of a radiation disaster. The FDA has granted Fast Track status to entolimod and Orphan Drug status for prevention of death following a potentially lethal dose of total body irradiation during or after a radiation disaster.

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