$DPRX (Dipexium Pharmaceuticals, Inc.)

$DPRX {{ '2016-09-08T11:07:51+0000' | timeago}} • Announcement

$DPRX said the European Patent Office has issued a new Locilex patent in the European Union (EU). The patent claims are directed to novel formulation of Locilex, topical antimicrobial peptide formulated as topical cream, and use of Locilex as method of treating skin or wound infections. The issued patent has expiry date in June 2033.

$AGN {{ '2017-09-22T21:53:16+0000' | timeago}} • Announcement

$AGN received a Refusal to File letter from the US FDA on its Supplemental New Drug Application (sNDA) for Vraylar for treatment of negative symptoms associated with schizophrenia in adult patients. VRAYLAR is an oral antipsychotic approved in the US to treat schizophrenia. The FDA said the sNDA was not sufficient to permit a substantive review.

$AGN {{ '2017-09-22T14:30:34+0000' | timeago}} • Announcement

$AGN announced top-line results from new data for the Centaur Phase 2b study which supports the anti-fibrotic efficacy and safety of Cenicriviroc (CVC) for the treatment of liver fibrosis in adults with NASH. $AGN is currently enrolling patients in a 2,000 patient phase 3 clinical trial of CVC called the Aurora trial.

$AMGN {{ '2017-09-14T19:26:48+0000' | timeago}} • Announcement

$AMGN and $AGN said the FDA has approved their Mvasi for the treatment of five types of cancer. Amgen and Allergan's bevacizumab biosimilar is also undergoing review by the European Medicines Agency, following a Marketing Authorization Application submitted in December 2016.

$AMGN {{ '2017-09-14T19:26:21+0000' | timeago}} • Announcement

$AMGN and $AGN said the FDA has approved their Mvasi (bevacizumab-awwb) for the treatment of five types of cancer. The approval was based on totality of evidence from global development program showing Mvasi is highly similar to Avastin. Mvasi is the first anti-cancer biosimilar, as well as first bevacizumab biosimilar, approved by the FDA.

$AGN {{ '2017-09-08T19:54:30+0000' | timeago}} • Announcement

$AGN transferred all patents for its dry eye treatment drug Restasis to the St. Regis Mohawk tribe to protect the drug patents. The tribe has granted Allergan back an exclusive license for the drug. As per the agreement, the tribe will get $13.75MM as one-time payment, and potentially $15MM annually in royalties.

$AGN {{ '2017-08-29T10:53:21+0000' | timeago}} • Announcement

$AGN and its subsidiaries reached a settlement regarding its litigation with Famy Care Ltd. relating to the company's patent covering Restasis (Cyclosporine Ophthalmic Emulsion). All Famy Care litigation regarding Restasis patents will be dismissed and Famy Care will terminate its pending petitions for Inter Parties Review.

$VRX {{ '2017-08-08T18:56:32+0000' | timeago}} • Webcast

$VRX cuts FY17 revenue guidance by $200MM to about $8.70-8.90Bil. This reflects the loss of approx. $170MM of Dendreon revenues. The overall reduced outlooks is mostly due to the revised expectation of the struggling Dermatology business.

$VRX {{ '2017-08-08T18:56:03+0000' | timeago}} • Webcast

During 2Q17, $VRX announced the use of cash on hand to redeem $500MM of outstanding senior notes due 2018. Since 1Q16, the company reduced total debt to $4.8Bil. $VRX expects to exceed the commitment of paying down $5Bil of debt from divestiture proceeds and free cash flow before February 2018.

$VRX {{ '2017-08-08T18:54:54+0000' | timeago}} • Webcast

$VRX's dermatology business continues to underperform. To address the challenges, the company has stabilized Derm ASP and have rebranded the business unit as Ortho Dermatologics during 2Q17. The company launched SILIQ on July. 27, 2017 as the new product under this business unit.

$ZTS {{ '2017-08-08T18:36:56+0000' | timeago}} • Webcast

$ZTS stated that its key markets in Europe performed well in 2Q17, the UK and Germany leading with 12% and 8% operational growth respectively. The growth was driven primarily by strong Apoquel sales.

$ZTS {{ '2017-08-08T15:06:46+0000' | timeago}} • Infographic

$ZTS Zoetis, Inc Segment Revenue Comparison Q2 2017

$VRX {{ '2017-08-08T14:16:40+0000' | timeago}} • Announcement

For FY17, $VRX lowered its revenue to about $8.70-8.90Bil from $8.90-9.10Bil. The company also plans to exceed commitment to pay down $5Bil in debt from divestiture proceeds and free cash flow before February 2018.

$VRX {{ '2017-08-08T14:07:13+0000' | timeago}} • Announcement

$VRX, Quebec-based drugmaker, reported 8% drop in its 2Q17 revenue to $2.23Bil. This decrease was mainly due to decline in volume and pricing of its U.S. Diversified Products segment. The company's net loss narrowed to $38MM, or $0.11 per share, compared to $302MM or $0.88 per share during 2Q16, mostly due to progress in debt reduction.

$VRX {{ '2017-08-08T12:03:05+0000' | timeago}} • Infographic

$VRX Valeant Pharmaceuticals International Earnings AlphaGraphics: Q2 2017 highlights

$ZTS {{ '2017-08-08T11:57:37+0000' | timeago}} • Announcement

$ZTS revenue in the US segment was $623MM in 2Q17, an increase of 5%, as sales of companion animal products grew 7%. Meanwhile, in the International segment, a 12% growth in companion animal products lifted revenue 5% to $634MM.

$ZTS {{ '2017-08-08T11:44:20+0000' | timeago}} • Announcement

$ZTS updated its guidance for FY17, and now expects revenue between $5.15-5.25Bil. While GAAP EPS is anticipated between $2.12 and $2.21, adjusted diluted EPS is predicted to be $2.30-2.37.

$ZTS {{ '2017-08-08T11:39:52+0000' | timeago}} • Announcement

Animal health company $ZTS reported 2Q17 revenue of $1.3Bil, up 5%, helped by higher sales in companion animal products in both the US and International segments. Net income grew 10% to $247MM, or $0.50 per share. On a adjusted basis, $ZTS earned $261MM, or $0.53 per share during the quarter.

$ZTS {{ '2017-08-04T18:38:36+0000' | timeago}} • Announcement

$ZTS, an animal health company, has appointed Linda Rhodes to its BoD, effective Aug. 3, 2017. She will serve on the Quality and Innovation Committee of the Board.

$AGN {{ '2017-08-03T19:43:47+0000' | timeago}} • Announcement

"With our strong first half performance and solid outlook for the remainder of the year, we are raising our full-year guidance,” said CEO Brent Saunders. For FY17, $AGN expects sales to be $15.85-16.05Bil, up from the prior estimate of $15.8-16.0Bil. GAAP loss per share is expected to be $10.80-11.20 versus the previous range of $9.70-10.20.

$AGN {{ '2017-08-03T18:43:48+0000' | timeago}} • Announcement

$AGN, which owns 9.9% stake in $TEVA, reported a wider loss in 2Q17, hurt by the loss of patent exclusivity and lower revenues from certain drugs. Net loss attributable to ordinary shareholders was $796MM or $2.37 per share compared to $571MM or $1.44 per share a year ago. However, revenue rose 9% to $4.01Bil and adjusted EPS increased 20% to $4.02.

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