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News Breaks
March 20, 2014
09:25 EDTABBV, ABBV, ABBV, AMGN, AMGN, AMGN, CELG, CELG, CELG, GILD, GILD, GILD, INCY, INCY, INCY, JNJ, JNJ, JNJ, NVS, NVS, NVS, PCYC, PCYC, PCYC, RHHBY, RHHBY, RHHBYPiper Jaffray's biopharm analyst holds an analyst/industry conference call
Analyst Schimmer, along with Dr. Munib Mundia, CEO of South Nassau Oncology, review CLL and other evolving hematological malignancies with relevant companies PCYC, JNJ, CELG, GILD, INCY, AMGN, ABBV, NVS, RHHBY on an Analyst/Industry conference call to be held on March 21 at 10 am.
News For ABBV;AMGN;CELG;GILD;INCY;JNJ;NVS;PCYC;RHHBY From The Last 14 Days
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April 9, 2015
09:10 EDTPCYCPharmacyclics' Imbruvica shows positive Phase II data
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06:12 EDTGILDSovaldi prices causes Medicaid spending for hepatitis C drugs to soar, WSJ says
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April 8, 2015
16:22 EDTNVSOn The Fly: Closing Wrap
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15:19 EDTRHHBYRoche says receives European approval for Avastin plus chemotherapy
Roche announced that the European Commission approved Avastin -- bevacizumab -- in combination with standard chemotherapy for the treatment of adult patients with persistent, recurrent or metastatic carcinoma of the cervix. The EU approval was based on the significant survival benefit in the pivotal GOG-0240 study, which showed that women who received Avastin plus chemotherapy had a statistically significant 26% reduction in the risk of death, representing a median improvement in survival of nearly four months, compared to women who received chemotherapy alone.
14:23 EDTNVSAdditional bidders for Perrigo could emerge after Mylan offer, says Stifel
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09:23 EDTJNJJohnson & Johnson April volatility elevated into Q1 and outlook
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07:24 EDTJNJNeurotechnology Industry Organization to hold a conference
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05:30 EDTABBVEnanta announces data on regimens containing protease inhibitors paritaprevir
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April 7, 2015
17:58 EDTGILDGilead submits NDA for investigational combination for treatment of HIV-1
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16:00 EDTGILDOptions Update; April 7, 2015
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07:31 EDTABBVBiogen to present data on neurological disease therapies at AAN meeting
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07:24 EDTCELGCelgene Otezla has growing opportunity, says Bernstein
After interviewing small groups of New York City area dermatologists, Bernstein believes that Celgene's psoriasis,treatment, Otezla, has a growing opportunity, due to its oral dosing, convenience, and lack of immunosuppression. The firm quotes doctors as saying that the drug serves as a useful "stepping stone," for patients who might need more intensive therapy, but want to postpone or avoid biologic Bernstein keeps a $158 price target and Outperform rating on Celgene.
07:14 EDTRHHBY, NVSEyeforpharma to hold a summit
Philadelphia 2015 Commercial Pharma Summit is being held in Philadelphia on April 7-8.
April 6, 2015
14:34 EDTJNJDepomed price target raised to $30 from $27 at Roth Capital
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09:36 EDTJNJActive equity options trading on open
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08:13 EDTNVSJuno Therapeutics announces patent litigation settlement
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07:36 EDTGILDGilead Q1 HCV revenue poised to beat expectations, says RBC Capital
After analyzing weekly prescription data, RBC Capital believes that Gilead's weekly hepatitis C prescriptions are tracking towards $3.5B-$3.6B of revenue from hepatitis C drugs for Q1, versus the consensus outlook of about $2.6B. The firm keeps an Outperform rating on Gilead.
06:21 EDTJNJJohnson & Johnson CEO comments on Asia expansion, WSJ reports
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05:19 EDTAMGNAmgen announces EC approval of Vectibix in combination with Folfiri
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April 5, 2015
14:43 EDTGILDActavis seeks FDA approval to market generic version of Gilead's Letairis
Actavis (ACT) on Friday, confirmed that it has filed an Abbreviated New Drug Application with the FDA seeking approval to market Ambrisentan Tablets, 5 mg and 10 mg. Actavis' ANDA product is a generic version of Gilead Science's (GILD) Letairis, which is a treatment for pulmonary arterial hypertension. Gilead Sciences and Royalty Pharma Collection Trust filed suit against Actavis on April 1, in the U.S. District Court for the District of Delaware seeking to prevent Actavis from commercializing its ANDA product prior to the expiration of U.S. Patent number RE42,462. The lawsuit was filed under the provisions of the Hatch-Waxman Act, resulting in a stay of final FDA approval of Actavis' ANDA for up to 30 months from the date the plaintiffs received notice of Actavis' ANDA filing or until final resolution of the matter before the court, whichever occurs sooner, subject to any other exclusivities. Based on available information, Actavis believes it may be a "first applicant" to file an ANDA for the generic version of Letairis and, should its ANDA be approved, may be entitled to 180 days of generic market exclusivity. For the 12 months ending December 31, Letairis had global sales of approximately $595M, according to Gilead.
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