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Stock Market & Financial Investment News

News Breaks
July 1, 2014
11:07 EDTPFE, ACTActavis could be potential target of Pfizer after Forest deal, says Leerink
News For ACT;PFE From The Last 14 Days
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April 28, 2015
07:12 EDTPFEPfizer lowers FY15 adjusted EPS view to $1.95-$2.05 from $2.00-$2.10
Consensus $2.07. Lowers FY15 revenue guidance to $44B-$46B from $44.5B-$46.5B, consensus $45.94B.
07:09 EDTPFEPfizer reports Q1 adjusted EPS 51c, consensus 49c
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April 27, 2015
15:04 EDTPFENotable companies reporting before tomorrow's open
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14:41 EDTPFEEarnings Watch: Pfizer up over 6% since its last earnings report
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12:47 EDTPFEPfizer technical comments before earnings
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09:03 EDTPFEChina Jo-Jo Drugstore signs incentive agreement with Pfizer subsidiary
China Jo-Jo Drugstores (CJJD) announced its subsidiary, Hangzhou Jiuzhou Grand Pharmacy Chain, has signed a new sales incentive agreement with Wyeth Pharmaceutical, a wholly owned subsidiary in China of Pfizer (PFE). The Agreement illustrated specific approaches and conditions of Jiuzhou Pharmacy's collaboration with Wyeth, including sales targets, promotional incentive to consumers, products and pricing methods. In return, Wyeth will fully support Jiuzhou Pharmacy with priority delivery, favorable purchase prices and promotional activities.
08:41 EDTPFETelegraph discusses potential takeover of GSK by Pfizer
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06:19 EDTPFEPharmceutical companies buy drugs and raises prices, WSJ reports
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April 24, 2015
09:27 EDTACTActavis' Dalvance shows positive Phase 3 results for skin infections
Actavis announced positive top-line results for study DUR001-303, a phase 3 study comparing a single 1500 mg dose of Dalvance with the same total dose given as two-doses one week apart, for the treatment of acute bacterial skin and skin structure infections caused by susceptible Gram-positive bacteria, including methicillin resistant Staphylococcus aureus. Preliminary top-line data demonstrated the 1500 mg single-dose of Dalvance achieved its primary endpoint of non-inferiority to the two-dose regimen at 48-72 hours after initiation of therapy. Actavis plans to file a supplemental New Drug Application with these data in Q3.
07:09 EDTACTCipher Pharmaceuticals announces Markman hearing in Absorica patent suit
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April 23, 2015
08:16 EDTACTActavis launches Avycaz anti-infective in U.S.
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April 22, 2015
07:37 EDTACTOrexigen and Takeda receive Paragraph IV certification notice
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April 21, 2015
10:01 EDTPFEPfizer receives FDA breakthrough therapy designation for Xalkori
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08:18 EDTPFEPain Therapeutics resumes responsibility for Remoxy
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08:06 EDTPFEPfizer says Phase 3 inotuzumab ozogamicin study met first primary endpoint
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April 20, 2015
16:22 EDTACTActavis reports CCO Charles Mayr to retire for health reasons
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08:12 EDTACTActavis's BOTOX label approved by FDA for spasticity treatment
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08:02 EDTPFEMerck KGaA, Pfizer initiate Phase III study with Avelumab
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07:18 EDTACTAmerican Academy of Neurology to hold annual meeting
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06:05 EDTPFEProvectus receives notice of allowance for PV-10 combined with other drugs
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