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Stock Market & Financial Investment News

News Breaks
June 23, 2014
07:39 EDTSHPG, ABBVShire CEO to highlight growth as rationale for turning down bid, FT says
Shire (SHPG) CEO Flemming Ornskov will lay out the company's financial case for independence, centered on highlighting its status as one of the fastest-growing companies in the pharmaceuticals industry, when the it holds a conference call with investors later today to explain why it turned down the latest bid made by AbbVie (ABBV), according to Financial Times. Reference Link
News For SHPG;ABBV From The Last 14 Days
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September 18, 2014
11:15 EDTABBVRepros sinks after panel backs tests for testosterone therapies
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06:10 EDTABBVFDA panel votes 20-1 to study changes to testosterone therapies
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September 17, 2014
07:43 EDTSHPGBofA/Merrill to hold a conference
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September 16, 2014
11:51 EDTSHPGOECD looks to close tax loopholes with new proposals
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September 15, 2014
10:55 EDTABBV, SHPGRegulators to determine AbbVie, Shire deal by next month, Reuters says
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08:01 EDTSHPGShire announces FDA acceptance for filing of sNDA for Vyvanse
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September 12, 2014
07:32 EDTABBVBiogen, AbbVie announce ZINBRYTA DECIDE Phase 3 study results
Biogen (BIIB) and AbbVie (ABBV) announced the full results from the Phase 3 DECIDE clinical trial, which show ZINBRYTA, dosed subcutaneously once a month, demonstrated a statistically significant improvement in reducing disease activity in people with relapsing-remitting multiple sclerosis compared to AVONEX. These results are being presented at the Sixth Triennial Joint Meeting of the Americas Committee for Treatment and Research in Multiple Sclerosis and the European Committee for Treatment and Research in Multiple Sclerosis. Patients on ZINBRYTA demonstrated a statistically significant 45% reduction in annualized relapse rate compared to patients treated with AVONEX. Based on the efficacy and safety data from the ZINBRYTA clinical development program, Biogen Idec and AbbVie plan to file marketing applications for ZINBRYTA with regulatory authorities during 1H15.
September 11, 2014
05:34 EDTABBVAbbVie reports Humira Phase 3 trial meets primary endpoint
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September 10, 2014
10:24 EDTABBVEnanta announces AbbVie initiated Phase 2b trial with ABT-493
Enanta (ENTA) announced that AbbVie (ABBV) initiated a phase 2b clinical study with ABT-493, Enantas next-generation protease inhibitor. ABT-493 is the second clinical-stage protease inhibitor candidate developed within the Enanta-AbbVie collaboration. The phase 2b study being conducted by AbbVie will evaluate the safety and efficacy of ABT-493 co-administered with ABT-530 in HCV patients. AbbVie has informed Enanta that results from this trial are expected in 2015 and AbbVie plans to start phase 3 development of the combination next year.
08:37 EDTSHPGMedgenics appoints Scott Applebaum as Chief Legal Officer
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07:06 EDTSHPGSangamo plans to submit IND application for hemophilia B in 2Q15
Sangamo BioSciences (SGMO) plans to submit an Investigational New Drug application for the treatment of hemophilia B in Q2 2015. This program, partnered with Shire (SHPG), is the first therapeutic application of Sangamo's zinc finger nuclease-mediated In Vivo Protein Replacement Platform. Sangamo is developing the IVPRP as a generally applicable strategy to provide a one-time, permanent genetic cure for monogenic diseases that are currently managed by protein replacement therapy, which involves costly repeat infusions over the lifetime of the patient.

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