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Stock Market & Financial Investment News

News Breaks
July 11, 2014
07:36 EDTGILD, JNJJohnson & Johnson Q2 EPS likely to exceed expectations, says Bernstein
Bernstein predicts that Johnson & Johnson will report higher than expected Q2 EPS, driven by its pharmaceuticals business. However, the firm warns that the growth of the company's pharmaceutical business could slow as the company's Olysio drug encounters more competition from Gilead's (GILD) Sovaldi. The firm keeps an Outperform rating on Johnson & Johnson.
News For JNJ;GILD From The Last 14 Days
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April 13, 2015
16:01 EDTGILDOptions Update; April 13, 2015
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15:38 EDTJNJNotable companies reporting before tomorrow's open
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15:08 EDTJNJJohnson & Johnson April 100 straddle priced for 2.2% movement into Q1
14:07 EDTJNJEarnings Watch: Johnson & Johnson shares down slightly since last earnings
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13:28 EDTJNJJohnson & Johnson April volatility elevated into Q1 and outlook
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11:12 EDTJNJJohnson & Johnson technical notes before earnings
Leading up to earnings, the shares have been trading in a narrow range largely bound by $98 at the low and $103 at the high. This trading range was preceded by a decline from the 52-week high set back in the fall of 2014. In a longer time frame, the current trading action is part of a larger potential topping process, with $95 as the midpoint. On worse than expected news, the low bound at $98 would be first important support. A breakdown below $98 would see next support at $95. A move below $95 would confirm the topping process and break the long-term uptrend. Support below $95 would be at $93.94. If results and outlook are better than expected, first resistance would be at the top of the range at $103. Next resistance would then be at $105.36. A move above that level would see $107.10, and then 52-week high and life high at $109.49 as next potential upside objectives.
09:34 EDTGILDActive equity options trading on open
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April 10, 2015
16:05 EDTGILDOptions Update; April 10, 2015
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14:39 EDTJNJJohnson & Johnson April volatility elevated into Q1 and outlook
Johnson & Johnson April call option implied volatility is at 20, May is at 16, June is at 15, October is at 14; compared to its 26-week average of 16 according to Track Data, suggesting large near term price movement into the expected release of Q1 results on April 14.
April 9, 2015
09:25 EDTJNJPiper Jaffray pharmaceuticals analysts hold an analyst/industry conference call
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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
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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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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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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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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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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