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Stock Market & Financial Investment News

News Breaks
November 14, 2012
10:55 EDTABT, ABT, AZN, AZN, CELG, CELG, INCY, INCY, LLY, LLY, PFE, PFE, RIGL, RIGLLeerink's major pharmaceuticals and biotech analysts hold a conference call
Major Pharmaceuticals Analyst Fernandez and Biotech Analysts Kozul and Liang provide insights from the American College of Rheumatology's Annual Meeting on an Analyst/Industry conference call. Relevant covered companies ABT, AZN, CELG, INCY, LLY, PFE and RIGL may be included on the Analyst/Industry conference call to be held on November 14 at 11 am.
News For ABT;AZN;CELG;INCY;LLY;PFE;RIGL From The Last 14 Days
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March 20, 2015
09:45 EDTCELGActive equity options trading on open
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09:01 EDTLLYEli Lilly up 2% to $75.75 in pre-market trading
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08:01 EDTLLYEli Lilly and Innovent Biologics announce strategic alliance
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07:55 EDTAZN, PFEAstraZeneca seen as potential target again if oncology drugs lag, Bloomberg says
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07:41 EDTLLY, PFE, CELGAmerican Academy of Dermatology to hold annual meeting
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06:26 EDTCELGCelgene price target raised to $144 from $135 at Piper Jaffray
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March 19, 2015
11:00 EDTPFEPfizer participates in a conference call with Bernstein
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09:37 EDTCELGActive equity options trading on open
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08:37 EDTAZNNektar and Daiichi Sankyo to commercialize Movantik in the U.S.
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08:08 EDTLLYEli Lilly and Hanmi sign license and collaboration agreement
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March 18, 2015
17:09 EDTPFEPfizer CAPiTA published in New England Journal of Medicine
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17:07 EDTCELGCelgene GED-0301 Phase II data published in New England Journal of Medicine
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12:48 EDTLLYFly Watch: Biogen predicted to report strong Alzheimer's data this Friday
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07:46 EDTLLYLilly Roche would have upbeat read through from strong BIIB data, says Bernstein
Bernstein notes that the data for Biogen's (BIIB) Alzheimer's treatment, due to be released on Friday, is widely expected to be positive. The firm thinks that positive data would boost the outlook for similar Alzheimer's drugs being developed by Eli Lilly (LLY) and Roche (RHHBY), since consensus estimates for those drugs are low. The firm keeps Outperform ratings on Eli Lilly and Roche.
March 17, 2015
14:10 EDTAZNIGI Laboratories recent sell-off a buying opportunity, says Craig-Hallum
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05:32 EDTINCYIncyte announces Novartis receives EC approval for Jakavi
Incyte (INCY) announced that Novartis (NVS) received approval from the European Commission for Jakavi for the treatment of adult patients with polycythemia vera, or PV, who are resistant to or intolerant of hydroxyurea. Jakavi is the first targeted treatment approved by the European Commission for these patients. Under the Incyte-Novartis Collaboration and License Agreement signed in 2009, Novartis received exclusive development and commercialization rights to ruxolitinib outside of the United States for all hematologic and oncologic indications, and sells ruxolitinib under the name Jakavi. Ruxolitinib is marketed by Incyte in the United States as Jakafi. Jakafi is approved by the FDA for treatment of people with polycythemia vera who have had an inadequate response to or are intolerant of hydroxyurea. Jakafi is also indicated for treatment of people with intermediate or high-risk myelofibrosis, or MF, including primary MF, post–polycythemia vera MF, and post–essential thrombocythemia MF.
March 16, 2015
07:30 EDTAZNAmerican College of Cardiology to hold an expo
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07:27 EDTLLYBiodel BIOD-961 Phase 1 clinical trial meets primary efficacy endpoint
Biodel (BIOD) announced positive preliminary results from Study 6-101, a Phase 1 clinical trial comparing Biodel's lyophilized glucagon formulation BIOD-961, designed for use in a proprietary Glucagon Emergency Management, or GEM, auto-reconstitution device, to Eli Lilly's (LLY) Glucagon Emergency Rescue Kit and Novo Nordisk's GlucaGen HypoKit, which are marketed for the treatment of severe hypoglycemia. Study 6-101 was a randomized, single-center, double blind, six-period cross over study in 15 healthy volunteers who received each glucagon administered subcutaneously, or SC, and intramuscularly, or IM, in a randomized treatment sequence. The objectives of the study were to compare the pharmacokinetic, or PK, profiles, the pharmacodynamic, or PD, glucose, responses, and the PK/PD relationships of IM and SC dosing, as well as to assess safety profiles of the three test glucagons. Study 6-101 was a Phase 1 randomized, single-center, double blind, six-period cross over study designed to evaluate the PK and PD profiles of BIOD-961 compared to marketed glucagon formulations manufactured by Eli Lilly and Novo Nordisk. BIOD-961 is a lyophilized glucagon formulation designed for use in the GEM auto-reconstitution device. On six separate dosing days, each subject received 1 mg of one of the test glucagons delivered either SC or IM. Fifteen normal, healthy subjects were randomized into the study and ten completed all dosings. The objectives of the study were to compare the PK profiles, the PD responses, and the PK/PD relationships of IM and SC dosing, as well as to assess safety profiles of the three test glucagons. These data will facilitate selection of an appropriate marketed glucagon to use as a comparator in the planned pivotal study, in which the primary efficacy endpoint for approval is to demonstrate PK and PD bioequivalence of BIOD-961 to one of the marketed comparators.
06:40 EDTPFEPCSK9 studies show potential improvement in heart health, WSJ says
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March 15, 2015
14:16 EDTABTAbbott announces 'favorable' data from MitraClip study
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