All Posts Tagged With: "NVS"

(BIIB) Biogen Analyst Neutral on Shares

We recently reiterated our Neutral recommendation on Biogen Idec (BIIB). Biogen is the market leader in therapies for the treatment of multiple sclerosis (MS). We believe the company will continue to retain a leading position in the MS market. Biogen’s largest product, Avonex,... 

21Jan2012 | | 0 comments | Continued

(NVS) Novartis’ Cancer Drug Afinitor Shows Promise for Breast Cancer

Novartis’ (NVS) cancer drug Afinitor took a significant step forward, as the company once again presented encouraging data from late-stage trials of Afinitor for the treatment of breast cancer, an indication for which management estimates sales potential in excess of $1 billion.... 

12Dec2011 | | 0 comments | Continued

(EU) Emerging Markets: The Way Forward

According to Irish orator, philosopher, & politician Edmund Burke, change is the most powerful law of nature. The winds of change seem to be sweeping across the pharmaceutical industry as well. Until recently, most commercialization efforts were focused on the U.S. —... 

7Dec2011 | | 0 comments | Continued

(MYL) Mylan Earns FDA Approval

Generic maker, Mylan Inc. (MYL) recently announced that its Indian subsidiary Mylan Laboratories has received tentative approval from the US Food & Drug Administration (FDA) for a fixed-dose combination of generic versions of Bristol Myers Squibb’s (BMY) drug Reyataz and... 

5Dec2011 | | 0 comments | Continued

(ALNY) Alnylam Pharmaceuticals Completes Trial Enrollment

Alnylam Pharmaceuticals Inc. (ALNY) recently announced it has completed enrollment in a mid-stage study of its pipeline candidate ALN-RSV01, an RNA interference technology (RNAi) therapeutic being studied for the treatment of respiratory syncytial virus (RSV) infection. The study... 

2Dec2011 | | 0 comments | Continued

(MYL) Mylan Approved for Zinecard Generic

Mylan, Inc.’s (MYL) generic business was boosted further with the approval from the U.S. Food and Drug Administration (FDA) for its generic version of Pharmacia & Upjohn’s Zinecard injection. Zinecard injection, which is a chemoprotective agent, recorded revenue of... 

1Dec2011 | | 0 comments | Continued

(NVS) Novartis’ Rasitrio Cleared in European Union

Novartis (NVS) recently announced that its triple combination hypertension pill Rasitrio has been cleared in the European Union (EU). Rasitrio combines the currently marketed hypertension pill Razilez (marketed as Tekturna in the US) with amlodipine and hydrochlorothiazide (HCT).... 

28Nov2011 | | 0 comments | Continued

(MYL) Mylan Settles with Novartis

Mylan, Inc. (MYL) recently announced a settlement agreement with Novartis (NVS) relating to the generic version of Novartis’ bioidentical estrogen therapy Vivelle-Dot. As a result of the resolution, the lawsuit filed by Novartis will be dismissed and Mylan can launch a generic... 

28Nov2011 | | 0 comments | Continued

(ALNY) Alnylam Pharmaceuticals Reveals ALNTTR01 Trial Data

Alnylam Pharmaceuticals Inc. (ALNY) recently presented data from an early stage study of its pipeline candidate ALN-TTR01 at a scientific conference in Japan. ALN-TTR01 is a systemically delivered RNA interference technology (RNAi) therapeutic that employs a first-generation... 

28Nov2011 | | 0 comments | Continued

(MNTA) Momenta Pharmaceuticals and Novartis AG Sue Watson Pharmaceuticals

Momenta Pharmaceuticals, Inc. (MNTA) and Novartis AG (NVS) filed a lawsuit against Amphastar Pharmaceuticals, Inc. and Watson Pharmaceuticals Inc. (WPI) regarding the generic version of Sanofi-Aventis’ (SNY) Lovenox. The lawsuit was filed in United States District Court for... 

24Sep2011 | | 0 comments | Continued

(MYL) Mylan Settles with Roche for Xeloda

Mylan Inc. (MYL) recently announced that it has entered into a settlement and license agreement with Roche (RHHBY) bringing an end to its ongoing litigation with the latter relating to Roche’s cancer drug Xeloda. Mylan was looking to launch a generic version of the drug which... 

23Sep2011 | | 0 comments | Continued

(NVS) Novartis Drug Cleared in European Union for SEGA

Novartis (NVS) recently received a boost when its drug Votubia was approved for the treatment of subependymal giant cell astrocytomas (SEGA), a benign brain tumor associated with tuberous sclerosis (TS) in the European Union (EU). For the first time ever will such a medication... 

20Sep2011 | | 0 comments | Continued

(NVS) Novartis Neuroendocrine Tumors Drug Cleared in European Union

Novartis’(NVS) drug Afinitor was recently approved in the European Union (EU) for the treatment of patients with advanced neuroendocrine tumors (NET) of pancreatic origin with progressive disease. The drug is already approved in the US for the indication. The approval was based... 

11Sep2011 | | 0 comments | Continued

(TEVA) Teva Pharmaceutical Industries Earns Favorable Court Ruling

Teva Pharmaceutical Industries Ltd. (TEVA) recently received a boost with the US District Court for the Southern District of New York issuing a favorable ruling related to the company’s patent infringement lawsuit against Novartis AG (NVS)/Momenta Pharmaceuticals, Inc. (MNTA)... 

1Sep2011 | | 0 comments | Continued

(ALNY) Alnylam Pharmaceuticals Analyst Maintains Neutral Rating on Shares

We have maintained a Neutral rating on Alnylam Pharmaceuticals, Inc (ALNY) with a target price of $7.00 per share. Alnylam Pharmaceuticals Inc. is a biopharmaceutical company developing novel therapeutics based on a biological breakthrough technology known as RNA (Ribo Nucleic... 

30Aug2011 | | 0 comments | Continued

(MYL) Mylan Analyst Reaffirms Shares at Neutral

We have maintained our Neutral recommendation on Mylan Inc. (MYL) with a target price of $19.00 following an appraisal of second quarter 2011 financial results. Mylan’s second quarter 2011 earnings (excluding special items) of 52 cents per share were above the Zacks Consensus... 

25Aug2011 | | 0 comments | Continued

(HGSI) Human Genome Sciences Analyst Maintains Neutral Recommendation

We are maintaining our Neutral recommendation on Human Genome Sciences Inc. (HGSI) with a target price of $16.00. Human Genome, founded in 1992 and based in Rockville, Maryland, is a biopharmaceutical company. The US launch of Benlysta earlier in the year for treating patients... 

22Aug2011 | | 0 comments | Continued

(MYL) Mylan and Endo Pharmaceuticals in Legal Tussle

Mylan Inc. (MYL) recently announced that Endo Pharmaceuticals (ENDP) filed a patent infringement lawsuit in connection with an abbreviated new drug application (ANDA) filed by Mylan with the US Food and Drug Administration (FDA) for the generic version of Endo’s acute migraine... 

18Aug2011 | | 0 comments | Continued

(MYL) Mylan Beats Second Quarter Earnings on All Fronts

Mylan Inc.’s (MYL) second quarter 2011 earnings (excluding special items) of 52 cents per share were above the Zacks Consensus Estimate of 45 cents as well as the year-ago earnings of 37 cents per share. Earnings growth was driven by increase in generics revenue and improved... 

27Jul2011 | | 0 comments | Continued

(AIXG) Company News for July 20, 2011 – Corporate Summary

•    Coca-Cola Company (NYSE:KO) reported Q2 EPS of $1.20, ahead of the Zacks Consensus Estimate of $1.16 per share. Revenues for the quarter rose 47% year-over-year to $12.7 billion, beating the Zacks Consensus Estimate of $12.364 billion •    Bank of America (NYSE:BAC)... 

20Jul2011 | | 0 comments | Continued

(AAPL) 2011 Second Quarter Earnings Preview – Detailed

Earnings Preview 7/15/11 Second quarter earnings season is now under way, but things really start to move into high gear next week. There will be 348 firms reporting, and 108 of those are in the S&P 500. By next Friday we should have a very good handle on how the overall... 

18Jul2011 | | 0 comments | Continued

(RDY) Dr. Reddy’s Laboratories Earns FDA Approval for Generic

Dr. Reddy’s Laboratories (RDY) delivered yet another positive momentum within a week, as the US Food and Drug Administration (FDA) approved fondaparinux sodium injection, the company’s bioequivalent generic version of Arixtra. The drug is currently marketed by GlaxoSmithKline... 

14Jul2011 | | 0 comments | Continued

(MYL) Mylan Gets HIV Rights from Gilead

Mylan, Inc. (MYL) recently announced that its Indian subsidiary Matrix Laboratories has been granted future rights to produce and sell generic versions of three investigational HIV therapies of Gilead Sciences, Inc. (GILD), if and when approved. The agreement aims to expand access... 

14Jul2011 | | 0 comments | Continued

(NVS) Novartis Presents Afinitor Data

Recently, Novartis (NVS) presented data from a late-stage study (EXIST-1) of its cancer drug Afinitor (everolimus). The randomized, placebo-controlled, double-blind, multicenter study evaluated the safety and effectiveness of the drug compared to placebo for treating patients... 

12Jul2011 | | 0 comments | Continued

(NVS) Novartis AG’s Lung Drug Cleared in US

Novartis AG (NVS) recently announced that its once-daily long-acting beta2-agonist (LABA) Arcapta Neohaler (75 mcg) was cleared by the US Food and Drug Administration (FDA) for the long-term maintenance bronchodilator treatment of airflow obstruction in patients with chronic... 

11Jul2011 | | 0 comments | Continued

(WPI) Watson Pharmaceuticals Entangled in Legal Dispute

The legal tussle between Watson Pharmaceuticals Inc. (WPI) and Shire plc (SHPGY) intensified, with the latter filing a patent infringement case against Watson Pharma relating to Vyvanse. Vyvanse is indicated for the treatment of attention deficit hyperactivity disorder (ADHD)... 

8Jul2011 | | 0 comments | Continued

(NVS) Novartis AG’s Afinitor Impresses Again

It seems Novartis AG’s (NVS) breast cancer drug, Afinitor (everolimus), is getting into a habit of delivering positive news. Right after the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended approval of Afinitor last week... 

7Jul2011 | | 0 comments | Continued

(SHPGY) Shire Entangled in Legal Dispute

The legal tussle between Shire (SHPGY), Sandoz, Inc. — the generic arm of Novartis (NVS) and Amneal Pharmaceuticals — intensified with Shire filing a patent infringement case against the two companies relating to Vyvanse. Vyvanse is indicated for treating patients... 

7Jul2011 | | 0 comments | Continued

(AMD) Roche Holdings Gets Positive Data on Lucentis

Roche Holdings Ltd. (RHHBY) recently reported positive data from two late-stage studies (RISE and RIDE) on its eye drug, Lucentis. The studies were conducted to evaluate the safety and efficacy of the drug in patients suffering from diabetic macular edema (DME). DME leads to... 

29Jun2011 | | 0 comments | Continued

(NVS) Novartis AG Afinitor Backed in EU

Novartis AG (NVS) received a boost recently when the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended approval of its drug Afinitor for the treatment of subependymal giant cell astrocytomas (SEGA), a benign brain tumor associated... 

29Jun2011 | | 0 comments | Continued