Novartis milestones be proud ! Management take a bow !

Buh Bye $1.7 billion

THE ECONOMIC TIMES
25 Mar, 2013, 12.45PM IST, Kiran Kabtta Somvanshi,ET Bureau
Lupin stock vaults to 52-week high on generic launch of Novartis' Diovan

Lupin achieves an important milestone with the launch of Valsartan and Hydrochlorothiazide Tablets, the generic version of Novartis' hypertension drug Diovan HCT in the US. The launch marks yet another limited competition foray in the US generics market for the fourth largest pharma company in India.

The market for Diovan HCT stands at $ 1.7 billion currently with two generic players. With LupinBSE 0.21 % having already started shipping the product, it will be help it in garnering market share for itself in a limited competition scenario.

Lupin's stock has hit a 52-week high of Rs 638.65 on BSE today following the news of the launch. The stock has gained 25% in the last one year - and has been one of the best performing stocks among the frontline pharma companies. The company has had a strong growth in its revenues in the last four quarters and also posted improvement in its operating profit margins during this period.
 






Novartis blockbuster linked to retracted papers

29 Mar 2013 | 14:32 GMT | Posted by David Cyranoski | Category: Health and medicine


Japanese media is reporting some uncomfortable ties between Novartis and some suspicious Japanese research linked to Valsartan (diovan), a lucrative blood pressure drug.

Sales of the drug hit ¥119.2 billion in 2011, making it the top selling drug for Novartis’ Japanese subsidiary and the third-best selling drug in Japan. The boom in sales followed reports that it not only lowered blood pressure but also reduced the risk of stroke and heart attack. Novartis used the results in advertisements.

But then Hiroaki Matsubara, the Kyoto Prefectural University of Medicine professor heading the group that published those results, ran into trouble. In December 2012, the Japanese Circulation Society retracted two of Matsubara’s papers, citing “serious errors in data analysis” in both. A 2012 paper claimed the drug helped diabetics avoid heart disease. The other, from 2011, claimed benefits for high-risk hypertensive patients. Matsubara said the errors were accidental and stood by his conclusions. A university committee in January found no signs of misconduct.

But since then the situation has spiraled. In February, the European Society of Cardiology retracted a similar 2009 paper on Valsartan by Matsubara. The notice raised the level of alarm: “Critical problems existed with some of the data reported in the above paper.”

Since then the Japanese Circulation Society has requested another investigation by Matsubara’s university. On February 28, he resigned. A day later the university began an investigation.

Novartis has maintained its distance from the research. When it was revealed that a scientist working for Novartis Pharma co-authored an earlier study with the group, also on Valsartan, but used an Osaka City University affiliation, Novartis responded by saying that its employee has an adjunct position at the university and “being famous in the statistician community, merely gave advice on what type of statistical analysis to use.” Yesterday, The Mainichi newspaper also reported that Novartis invested ¥100 million in the group’s research.
 












Domo Origato Mr Novato

Novartis blockbuster linked to retracted papers

29 Mar 2013 | 14:32 GMT | Posted by David Cyranoski | Category: Health and medicine


Japanese media is reporting some uncomfortable ties between Novartis and some suspicious Japanese research linked to Valsartan (diovan), a lucrative blood pressure drug.

Sales of the drug hit ¥119.2 billion in 2011, making it the top selling drug for Novartis’ Japanese subsidiary and the third-best selling drug in Japan. The boom in sales followed reports that it not only lowered blood pressure but also reduced the risk of stroke and heart attack. Novartis used the results in advertisements.

But then Hiroaki Matsubara, the Kyoto Prefectural University of Medicine professor heading the group that published those results, ran into trouble. In December 2012, the Japanese Circulation Society retracted two of Matsubara’s papers, citing “serious errors in data analysis” in both. A 2012 paper claimed the drug helped diabetics avoid heart disease. The other, from 2011, claimed benefits for high-risk hypertensive patients. Matsubara said the errors were accidental and stood by his conclusions. A university committee in January found no signs of misconduct.

But since then the situation has spiraled. In February, the European Society of Cardiology retracted a similar 2009 paper on Valsartan by Matsubara. The notice raised the level of alarm: “Critical problems existed with some of the data reported in the above paper.”

Since then the Japanese Circulation Society has requested another investigation by Matsubara’s university. On February 28, he resigned. A day later the university began an investigation.

Novartis has maintained its distance from the research. When it was revealed that a scientist working for Novartis Pharma co-authored an earlier study with the group, also on Valsartan, but used an Osaka City University affiliation, Novartis responded by saying that its employee has an adjunct position at the university and “being famous in the statistician community, merely gave advice on what type of statistical analysis to use.” Yesterday, The Mainichi newspaper also reported that Novartis invested ¥100 million in the group’s research.

Must be Novartis silver samurai !
 












Patent’s Defeat in India Is Key Victory for Generic Drugs

By GARDINER HARRIS

Published: April 1, 2013


NEW DELHI — The Indian Supreme Court rejected a Swiss drug maker’s patent application for a major cancer drug Monday in a landmark ruling that will allow poor patients continued access to many of the world’s best drugs, at least for a while.

India Ink: Health Care Advocates Cheer Supreme Court Decision (April 1, 2013)

The ruling allows Indian makers of generic drugs to continue making copycat versions of the Novartis drug Gleevec — spelled Glivec in some markets, like Europe — which can have a seemingly miraculous effect on some forms of leukemia.

But the ruling’s effect will be felt well beyond the limited number of patients in India who need Gleevec, because it will help maintain India’s role as the world’s most important provider of inexpensive medicines, which is critical in the global fight against HIV/AIDS and other diseases. Gleevec can cost as much as $70,000 per year, while Indian generic versions cost about $2,500 year.

“The judgment in the Novartis case is a victory for patients both in India and around the world,” Dr. Yusuf K. Hamied, chairman of Cipla, an Indian generic drug giant, wrote in an e-mail. “India, being the pharmacy capital of the world, can continue to produce affordable, high-quality medicines without the threat of patents for minor modifications of known medicines.”

In a televised interview, Ranjit Shahani, vice chairman of Novartis’s Indian subsidiary, said that India would suffer as a result of the ruling because companies like Novartis would invest less money in research there. “We will continue with our investments in India, even though cautiously,” he said. “We hope that the ecosystem for intellectual property in the country improves.”

The ruling is a landmark in one of the most important economic battles of the 21st century, in which rich nations that increasingly rely on the creation of idea-based products like computer programs and medicines try to compel mostly poor countries that make physical things like clothing and toys to pay for their ideas.
 






India Court Ruling Against Novartis Is Dark Omen For Big Pharma

Nigam Arora Nigam Arora, Contributor

It is official: India is siding with poor cancer patients over profits for multinational drug giants.

The Supreme Court of India has rejected a plea by Swiss pharma giant Novartis that ends the seven-year legal battle to restrict Indian companies from copying blood cancer drug Glivec. Novartis had filed a plea with the Supreme Court after the Intellectual Property Appellate Board had rejected a patent claim for Glivec.

Glivec is marketed as Gleevec in the United States. In 2001, Time magazine called it the magic bullet for cancer patients. The drug was originally developed as Imatinib using rational drug design after Philadelphia chromosome mutation was discovered.

In India, Glivec costs about 120,000 rupees for a one month dose. In contrast, generic copies by Indian companies cost about 8,000 rupees, or about $148 at current exchange rates.

The decision is being hailed by activists and has major implications for multinational pharmaceutical firms. The decision opens the door for Indian companies to continue to make generics of a large number of drugs that are under patent in the developed world.

The decision is also a big setback for the ever-greening strategy employed by big pharma. In this strategy, big pharma makes minor changes to extend patents.

Lately, American investors have shown irrational exuberance about pharmaceutical stocks. Pharmaceutical stocks have been one of the best performing groups.

Bulls on pharmaceutical stocks cite two reasons behind their analysis. First, they deem pharmaceuticals as safe at a time of uncertainty in Europe and slowing growth in China. The thinking goes that people will always need drugs. Second, pharmaceutical stocks typically pay high dividends and buying dividend stocks is in fashion because there are not many other places to get yield.

Bulls miss two key points. The fastest growing markets are not the developed markets, but the developing markets such as India. Now India has thrown down the gauntlet against big profits on branded drugs. My expectation is that most emerging markets will follow. In the long run, this is a very negative development for big pharma.

The second point is that it is easy to forget $15 trillion in debt at a time when the stock market is in party mode. The debt situation is partly exasperated by ever increasing spending on Medicare and Medicaid. In the long run, the growth of Medicare and Medicaid at present rates is unsustainable. At present Medicare and Medicaid do not obtain competitive pricing for drugs; this situation cannot last forever. Typically, branded drugs in the U. S. tend to cost more than many other places in the world.

Bulls are right that the drug lobby is strong and politicians prefer to kick the can down the road. However, sooner or later the pricing of branded drugs in the U. S. is bound to come under pressure and herein lies a valuable insight for the long-term investors. Investors may want to exercise caution in stocks of firms such as Novartis, Pfizer, Merck, Lilly, and Bristol-Myers. Aggressive investors can also take advantage of the present irrational exuberance to start slowly and cautiously building short positions in pharmaceuticals.

About Me: I am an engineer and nuclear physicist by background. I founded two Inc. 500 companies, and have been involved in over 50 entrepreneurial ventures. I am the chief investment officer at The Arora Report, which publishes four newsletters to help investors profit from change. Write me: Nigam@TheAroraReport.com. Follow me here and get email notification when I publish a new article
 






3 Apr, 2013, 03.36AM IST, Chidanand Rajghatta,TNN

Novartis patent case: Glivec developer Brian Druker hails SC ruling

WASHINGTON: Big Pharma found little support from the small guy on the street as the Indian Supreme Court's decision to reject patent claims of the drug maker NovartisBSE -0.08 % for its celebrated cancer medicine Glivec reverberated across the world.

The pharma lobby railed against the decision but the overwhelming sentiment, from physicians to politicians, from academia to media, particularly in a country groaning from the high cost of health care, was that the Indian judiciary did good by workaday people -- not just by the poor in the developing world but also those struggling in the developed world.

The pharma chums argument that denying patents to drug companies and eating into their profits will inhibit research investment into future wonder drugs was knocked down easily in the U.S, particular in the case of Glivec. The acclaimed drug, considered a magic bullet for leukemia, was actually developed jointly by Dr Brian Druker, director of the OregonBSE 4.47 % Health and Science University Knight Cancer Institute, in collaboration with Nicholas Lydon of Novartis. In that sense, it had some public funding.

Druker himself welcomed the Indian ruling, according to media reports. At the same time, he has also criticized the pharma majors' predatory pricing in the past, including in reference to Glivec.

The U.S spends more than $ 2.5 trillion, more than 15 per cent of its GDP, on health care -- more than any other country in the world -- with much less to show than other nations. Much of this is attributed to a broken health care system aggravated by predatory practices of the all-powerful pharmaceutical industry that spends enormous amounts on lobbying and reaps huge profits, to the dismay of even health care professionals.

The health care community also rejected Novartis contention that it was supplying Glivec free to most patients in India who were prescribed the drug, saying patients should not have to depend on the whims of the drug industry or voluntary programs. Among those welcoming the Indian decision was Doctors Without Borders (Medicines Sans Frontier), which depends largely on generics from India for worldwide operations.

"This is a huge relief for the millions of patients and doctors in developing countries who depend on affordable medicines from India, and for treatment providers like MSF," said Dr. Unni Karunakara, MSF's international president. "The Supreme Court's decision now makes patents on the medicines that we desperately need less likely."

"This marks the strongest possible signal to Novartis and other multinational pharmaceutical companies that they should stop seeking to attack the Indian patent law," Dr Karunakara added.

Even in the United States, where the pharma lobby is considered all-powerful because of its deep pockets and ability to influence legislation in Washington, the general sentiment went with the Indian decision with editorials and commentaries broadly sympathetic to the immediate needs of the poor against the arguments of the rich and powerful claiming to work in long term interests of the needy.

According to think-tank studies, the drug industry has spent more than a billion dollars since 2000 on lobbying, more than any other sector. The industry has more than 1200 registered lobbyists who strive to promote legislation friendly to the industry at the expense of patients.

Many of them sprang to Novartis' defense on Monday, pointing to what they saw as the folly of shooting down pharma majors' profit for short term gains for patients. Some of them tried to isolate India, which is seen as taking the lead role in the fight against branded drugs by the so-called generics.
 






Of course on April Fools Day Jose Jimenez says
"the industry needs to make big changes in order to survive in the long run, like redefining blockbusters and getting paid for positive outcomes instead of just transactions"
So what positive outcomes will we be achieving with garbage like Tekturna Jose ?
That little snafu in India was not some isolated event.
The case in Indian is the NUKE that will blast the pharma biz into low priced commodities
In other words , (most) pills will be like wheat & corn
Patients will not care what box they are in , who's name is on the box or where to box came from. It's all about the benjamins especially to the govts footing the tab.
& for the record all these 'traditional' pharma co's have as spotty a quality track record
as any factory in Shanghai or Mumbai.
Anyway that little case in India will do to pharma what cars did to horse & buggy .
In the meantime , to quote the esteemed Loki
"How desperate are you that you turn to such lost creatures ? "

Like say......Tekturna or Exelon patch
 






India rejects Novartis patent appeal

8 April 2013
Sarah Houlton

The court says the new polymorph of Glivec does not enhance its efficacy enough to warrant a patent
India’s Supreme Court has denied Novartis’ appeal against the decision to refuse patent protection for its anticancer drug Glivec (imatinib mesylate).

The company described the decision as a setback for patients that will hinder medical progress for diseases without effective treatment options. ‘We strongly believe that original innovation should be recognised in patents to encourage investment in medical innovation,’ said Novartis India’s managing director Ranjit Shahani.

The court’s decision met widespread dismay in industry. John Castellani, chief executive of US trade organisation PhRMA, described the decision as disappointing. ‘[It] marks yet another example of the deteriorating innovation environment in India,’ he said. ‘In order to solve the real health challenges of India’s patients, it is critically important that India promote a policy environment that supports continued research and development of new medicines for the health of patients in India and worldwide. Protecting intellectual property is fundamental to the discovery of new medicines.’

However, it was welcomed by humanitarian organisations such as Médicins Sans Frontières (MSF), which said that Indian law is designed to prevent drugs’ patent protection being extended through formulation modifications, and this was a ‘major victory’ for patient access to affordable medicines. ‘This is a huge relief for the millions of patients and doctors in developing countries who depend on affordable medicines from India,’ said MSF’s international president, Unni Karunakara.

Picking at patents

Before 2005, only manufacturing processes could be patented in India, not molecules. The result was a very strong generics industry, built on the skills of chemists who developed new ways to make drugs without infringing pharma companies’ process patents. Product patents were introduced so that India complied with the World Trade Organization’s Trade-Related Aspects of Intellectual Property Rights Agreement, or TRIPs.

However, numerous western pharmaceutical companies have struggled to patent their drug molecules in the country; for example, Pfizer was granted a patent for anticancer agent Sutent (sunitinib) in 2007, but this was revoked last year. Merck & Co is currently also suing Indian firm Glenmark over generic versions of its diabetes treatment Januvia (sitagliptin) and Janumet (sitagliptin plus metformin). The high court in Delhi has allowed the suit to proceed, but denied Merck an injunction to prevent Glenmark from selling its generic versions in the meantime. And even when patents are granted, India’s government can override them by issuing a ‘compulsory license’, as happened with Bayer’s anticancer drug Nexavar (sorafenib) last year.

Indian law requires certain pharmaceutical inventions to show ‘enhanced efficacy’, thus greatly limiting pharma companies’ ability to obtain patents on molecules, especially those that were already patented elsewhere before India introduced product patents.
 






MORE MANAGEMENT INCOMPETENCE

How the CSIRO cheated a global drugs giant

Date-April 11, 2013 Sunday Morning Herald

Linton Besser, Nicky Phillips

The CSIRO has duped one of the world's biggest pharmaceutical companies into buying anti-counterfeit technology which could be easily compromised - passing off cheap chemicals it had bought from China as a ''trade secret'' formula.

The Swiss-based multinational Novartis signed up two years ago to use a CSIRO invention it was told would protect its vials of injectible Voltaren from being copied, filled with a placebo and sold by crime syndicates.

"I'm sure you'll appreciate the importance of secrecy."

Police and drug companies are battling counterfeiters who are selling fake medicines that have killed hundreds of people. Last year Interpol seized 3.75 million units of fake drugs and arrested 80 people.

DataDot Technology: The joint venture between DataTrace DNA and CSIRO which convinced Novatiris to buy an easily compromised product.

The invention sold to Novartis to protect against such counterfeit attacks - a microscopic chemical powder painted on the neck of its Voltaren ampoules - was being marketed by DataTrace DNA, a joint venture of CSIRO and DataDot Technology, a publicly listed company.

But a Herald investigation has established that CSIRO officials and Datadot executives misled Novartis about the technology in order to close the deal, after receiving explicit internal warnings the Novartis code could be easily duplicated.

Now, hundreds of millions of Voltaren ampoules across the world could carry the easily compromised DataTrace product. The injectible version of the drug is not approved for use in Australia.

Three months before the deal was signed, the scientist working on the technology, Gerry Swiegers, issued a last caution against proceeding. ''The code which has been offered to Novartis may not be fit for purpose … because the code material is commercially available from a variety of vendors,'' Dr Swiegers wrote to DataTrace in March 2010. ''If there is a serious counterfeiting threat to the Novartis ampoules, then this code risks being quickly and easily cracked in a counterfeiting attack. Serious questions could then be raised, especially if the successful counterfeiting attack resulted in injury or death.''

But the deal went ahead anyway in July 2010. And despite having promised to supply a unique tracer code, DataTrace issued Novartis cheap tracer it had bought in bulk from a Chinese distributor.

The bulk tracer had been earmarked for low-risk applications with no real security concerns. But when DataTrace sold it to Novartis, it said the formula was a trade secret, and Novartis is believed to have been contractually forbidden from trying to identify its make-up.

Asked in general about industry practice, Jeff Conroy, the chief technology officer of Authentix, a rival company, said it was common ''to require either a non-disclosure agreement and/or a non-reverse engineering clause when supplying a security material''. It would be ''very typical'' to not disclose the precise material used in the tracer.

Had Novartis reverse-engineered the tracer potentially in breach of its contract, it would have been able to identify its components and check whether the phosphor formula was available elsewhere. In fact, at least two firms were selling the identical material to hundreds of firms around the world.

Damning internal documents seen by the Herald show DataTrace and some of the most senior officials at the CSIRO knew that Novartis was being misled in a deal believed to be worth $2.5 million.

On August 7, 2009, Greg Twemlow, the DataTrace manager who engineered the deal with Novartis, emailed CSIRO managers Peter Osvath and Geoff Houston with this subject line: ''Proposed answer to the question, 'is our Tracer code commercially available'.''

''This is how we propose to answer the question if it's posed. We want everyone answering consistently. Answer: The CSIRO will

make your Novartis codes using their Trade Secret methods and I'm sure you'll appreciate the importance of secrecy for Novartis and all of our clients. Having said that there may well be a possibility that aspects of the code could be simulated with commercially available products.''

But it was much more than a possibility. Mr Twemlow himself confirmed this was the case in a ''highly confidential'' paper he prepared for a January 2010 DataTrace meeting attended by CSIRO officials. ''We currently source end-product, ie we deploy the product as purchased by us for our clients,'' it said.

A leaked email list from one of the potential suppliers of the phosphor, a British company called Phosphor Tech, ''indicates that many hundreds of companies could be buying the same materials we use for Tracers''.

''The key question from our clients has generally been, 'Do we make our own Tracers?' Our answer has always been that CSIRO handles this.''

Mr Twemlow himself understood the risks, according to internal company correspondence. ''Greg, when we talked just before Xmas [2009] you indicated that if we used Chinese lamp phosphors in high security applications, then it would be 'only a matter of time' (your words, not mine) before the system would be copied and compromised,'' Dr Swiegers wrote in January 2010.

''The lamp phosphors were meant for bulk applications, not high security ones. This is especially significant in pharmaceutical applications where counterfeit pharmaceuticals could have serious safety implications (life-and-death implications).''

Mr Twemlow said on Wednesday he was bound by confidentiality agreements but that ''it was a detailed and complex proposal to a large company … I was the sales guy.'' He said the final decision on the transaction was taken by others.'' Dr Swiegers, who was retrenched from CSIRO after a bitter falling-out, has since been agitating for reform of the peak scientific body.

Counterfeiting was such a serious commercial and public health risk that Novartis went to extraordinary lengths to ensure DataTrace and CSIRO had security measures in place to prevent the code from being cracked.

In April 2010, Dr Osvath completed a Novartis questionnaire guaranteeing the ''protocols'' CSIRO would employ ''for secure freight logistics … with appropriate security measures''.

The next month he sent an email to Mr Twemlow and others regarding an $8000 quote to create a ''secure lab'' at the organisation's Clayton campus in Melbourne. The money was spent installing a wall and security access readers on the lab doors - features which may have assisted in convincing Novartis that its tracer code could not be compromised.

''I was wondering whether it would also suit DataTrace's purposes, to have signage on the door, identifying the area as a 'DataTrace Lab','' he wrote. ''While it will be used for other purposes … it might be useful for you, and not stretching the reality too far.''

In fact, a team of auditors from Novartis had already visited Australia to check on the company's claims. In August 2009, the team visited CSIRO's Clayton campus and was given a series of presentations by the company, including one by Dr Osvath on ''CSIRO: secure supply and support for DataTrace DNA/Novartis project''.

In July 2010 DataTrace announced a five-year deal with an unnamed pharmaceutical company to the stock exchange.

Just three months after the deal was announced to the market, CSIRO sold its 50 per cent stake of the company, worth $1.3 million, for 8.93 per cent of DataTrace's parent company, DataDot Technology.


Read more: http://www.smh.com.au/technology/sc...drugs-giant-20130410-2hluf.html#ixzz2Q5z5RGNv
 






Novartis, minister launch inquiries
By Linton Besser, Nicky Phillips
April 12, 2013, 3 a.m

Global drug giant Novartis has begun an ''internal investigation'' into a five-year deal it signed with a CSIRO spin-off company to buy an anti-counterfeit technology that the CSIRO and its partner knew could be compromised.

Novartis bought what it was told was a custom-designed invisible ''tracer'' that would protect millions of ampoules of injectible Voltaren, widely sold overseas but not in Australia, from the threat of the booming black market trade in counterfeit medicines.

But a Herald investigation revealed on Thursday that DataTrace DNA Pty Ltd, a joint venture between the CSIRO and public company DataDot Technology Ltd, instead issued Novartis with widely available tracer material it had bought from China and which it was warned was insufficient for a pharmaceutical application.

Science Minister Don Farrell has demanded the CSIRO investigate the issue and report back to him, and opposition science spokeswoman Sophie Mirabella is calling for an independent inquiry into the CSIRO to address this ''very serious allegation''.

''There needs to be an independent investigation,'' she said. ''Obviously something has gone very wrong.''

Alexandra Suvajac, a Novartis Australia spokeswoman, said the company had several measures to ensure the safe use of its drugs that were ''not compromised by the allegations around the use of this technology''.

''I can confirm we are undertaking an internal investigation of the matter,'' she said.

''Novartis is aware of the story reported today and cannot comment further on the ongoing investigation.''

The CSIRO said it was ''making inquiries to establish the facts and test the veracity of the claims in so far as they relate to CSIRO''.

Shares in DataDot Technology have been put into a trading halt until Monday. Company secretary Graham Loughlin requested the halt as a result of Thursday's press coverage of the allegations.

DataTrace was half-owned by CSIRO when it sold the anti-counterfeit technology to Novartis, which had sought a method to protect its injectible drugs, made in Egypt, Slovakia and Switzerland.

DataTrace had several times assured Novartis the tracer was made under secure conditions in a CSIRO laboratory in Melbourne.

In fact, the company issued it with phosphor-based tracer bought from a lighting supplier in China that was considered sufficient only for low-security applications, such as batch and stock control or sorting industrial commodities.

Do you know more?

investigations@smh.com.au
 












WHATCHYA YA GONNA DO ? WHATCHYA GONNA DO WHEN THEY COME FOR YOU

Novartis Didn't Properly Test Hypertension Drugs, Suit Says
by Juan Carlos Rodriguez
Law360, New York (April 16, 2013, 1:51 PM ET) --

Novartis AG has been hit with a lawsuit in New Jersey federal court alleging a woman was injured by the company’s hypertension drugs Valturna and Tekturna because the company didn’t test them properly, according to a notice of removal filed Friday.

Plaintiff Dottie Dodson said she was prescribed Valturna in 2010 in combination with Benicar, another anti-hypertensive drug, and later in combination with Tekturna, leading to chronic kidney disease and end-stage renal failure in 2011. She alleges Novartis discovered the drugs should not be taken in...
 






U.S. sues Novartis over alleged fraudulent kickbacks
Reuters – 29 mins ago...
April 1, 2013. REUTERS/Vivek Prakash

(Reuters) - Novartis AG was sued on Tuesday by the United States, which accused the Swiss drug maker of using kickbacks to induce pharmacies to steer thousands of patients to its drug Myfortic, which is used for people who have undergone kidney transplants.

U.S. Attorney Preet Bharara in Manhattan said Novartis disguised the kickbacks as rebates and discounts, in a scheme that caused Medicare and Medicaid to issue tens of millions of dollars of reimbursements based on false, tainted claims.

"Novartis co-opted the independence of certain pharmacists and turned them into salespeople," Bharara said in a statement.

The lawsuit seeks civil penalties and triple damages from Novartis for violating the federal False Claims Act. Bharara also said Novartis is a "repeat offender," having settled fraud charges linked to kickbacks fewer than three years ago.

A Novartis spokeswoman had no immediate comment.
 






Novartis to cut 300 jobs at Lincoln plant

7 hours ago • By MATT OLBERDING / Lincoln Journal star

(12) Comments

Novartis announced plans Wednesday to restructure operations at its plant at 10401 U.S. 6 east of Lincoln, including laying off 300 people.

After more than a year of trying to fix quality-control problems at its plant east of Lincoln, Novartis appears to be throwing in the towel.

The Swiss pharmaceutical company on Wednesday announced that it will drastically scale back its operations at the plant at 10401 U.S. 6 east of Lincoln and lay off 300 employees over the next two years, a 40 percent reduction of its workforce of around 750 people.

Novartis said the reduction in production at the Lincoln plant will enable the site to "focus on operational excellence with minimal product complexity."

In a news release, the company said that going forward it will make only Excedrin and TheraFlu in Lincoln, along with animal health product Sentinel.

"We have made the decision to focus this plant away from a pretty complex plant where we produce five different technologies to only two," CEO Joe Jimenez said in a conference call with financial analysts. "We are going to produce only solids and powders."

That means many well-known over-the-counter drugs that have been manufactured in Lincoln -- including Maalox, Bufferin and Triaminic -- will no longer be made here.

Novartis said many of those drugs are already being made by third-party manufacturers, which it declined to name.

Sentinel, an oral medication that prevents fleas and worms in dogs and cats, is the only product currently being shipped from Lincoln. Novartis did not give a timetable for restarting production of Excedrin and Theraflu products in Lincoln.

Jimenez said that despite the product cuts, the Lincoln plant will still produce 70 percent of the volume it did before the shutdown. He said the remaining 30 percent of production will go to third parties or other Novartis plants.

Julie Masow, a Novartis spokeswoman, said that while much progress has been made addressing problems at the Lincoln plant, "we still have more remediation work to do."

The company said that it underwent another inspection by the Food and Drug Inspection in February, which noted nine issues, mostly relating to the timeliness and completion of handling customer complaints.

That was a major issue among those that led to the plant's being shut down in December 2011.

Two FDA inspections that year, about five months apart, noted numerous instances of the company's not addressing consumer complaints and in some cases, ignoring them.

Those complaints included broken tablets as well as numerous instances of mixed tablets in drug products. In several incidents, the FDA inspectors said Excedrin caplets were mixed in with Excedrin tablets or gelcaps. In another instance, there was a report of unnamed foreign tablets in a package of the antacid Prevacid.

The most recent FDA inspection report was not available, but Novartis said it noted no problems related to manufacturing processes.

Masow said that by streamlining operations at the site and cutting the number of products produced there, the company will be able to create stronger quality systems and capabilities "that will ensure its long-term success."

She said the job cuts will come in phases, with plans to lay off 100 people late next month. Another round of about 100 layoffs is planned for early 2014, with the final 100 layoffs planned for by mid-to-late 2015.

Masow said the majority of the jobs that will be cut will be in production.

Those who lose their jobs will be offered a compensation package that includes severance pay and a retraining allowance, Masow said. Novartis will also continue to contribute to medical and dental costs for a period of time, she said, and will continue access to the Employee Assistance Program. The company also is hiring an outside firm to provide outplacement assistance to laid-off employees.

Novartis said Wednesday that impairment and severance costs related to the Lincoln operations will total about $100 million, and that the company already took a $51 million charge for those costs in the first quarter.

That will come on top of the losses the company has already incurred due to the plant being closed. For the calendar year 2012, the company's net sales were down almost $900 million for the consumer health division, which includes the Lincoln operation. Operating income was down almost $700 million for the division.

Novartis' announcement Wednesday marks the largest downsizing move by a local company since Kawasaki offered buyouts to 320 employees in May 2009.

“We are obviously disappointed at today’s news regarding the downsizing of the Novartis workforce," Lincoln Chamber of Commerce President Wendy Birdsall said in a statement.

"There have been very obvious issues with the Lincoln operation of Novartis that have been well publicized. These go well beyond the community and are part of the global decision-making of the company. We have offered to help wherever we can and continue to offer any services that the Chamber, Partnership (for Economic Development) or community at large can provide in order to get the facility back to full strength. We will begin working with our state and local workforce development resources to identify new opportunities for any displacements of people at the plant when they occur.”
 






Wall St Journal
4/26/2013

U.S. Accuses Novartis of Kickbacks
Prosecutors Allege Drug Maker Gave Physicians Lavish Dinners, Fishing Trips to Prescribe Pills.
By CHAD BRAY and JEANNE WHALEN


Federal prosecutors accused the U.S. unit of Novartis of paying kickbacks and providing lavish dinners to doctors to encourage them to prescribe their brand-name drugs to treat hypertension and other maladies.

The money, Novartis AG said, was for doctors to speak at educational programs around the U.S.
Federal prosecutors allege that many of those meetings took place at Hooters.

Those alleged junkets were among many outlined in a civil-fraud lawsuit filed in Manhattan federal court on Friday, in which prosecutors alleged the company's U.S. unit paid kickbacks and provided lavish dinners for doctors to encourage them to prescribe certain brand-name drugs to treat hypertension and other maladies.

The inducements, prosecutors said, included fishing trips off the Florida coast, and outings to restaurants like Nobu in Manhattan—as well as meals at Hooters around the country. Another outing allegedly was held at a salmon fishing lodge in Alaska, with the speaker receiving $750.

"It would have been virtually impossible for any presentation to be made" on a fishing boat, prosecutors said.

It was the second civil case federal prosecutors had brought in a week regarding alleged payment of kickbacks by the U.S. unit of the Swiss drug maker.
 






Global Post
Amy Silverstein April 27, 2013 14:58

Novartis took doctors to Hooters, lawsuit says

Drug company Novartis is accused of giving doctors unethical kickbacks.
this story is part of globalpost's continuing coverage of world business. for more visit our new business page.

Have you ever received a prescription that you didn't think you needed for some hardcore Novartis drugs? Bad news: your doctor may have sold you out for a Hooters waitress and some crispy chicken wings.

Novartis plied physicians with dinners, speaker fees, fishing trips and outings at Hooters restaurants to get them to prescribe patients more Novartis drugs, the US government alleges. The US made the claims in a lawsuit filed in Manhattan federal court

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“Novartis corrupted the prescription drug dispensing process with multimillion-dollar ‘incentive programs’ that targeted doctors who, in exchange for illegal kickbacks, steered patients toward its drugs,” Manhattan US Attorney Preet Bharara said in a statement to reporters.

The charges were first made by a former Novartis employee turned whistle-blower. The whistle-blower filed the lawsuit in 2011, the New York Times reported, but the federal government has only recently joined it.

In an email, Novartis told the Wall Street Journal that physician speaker programs are an "accepted and customary practice in the industry," which will probably not improve your faith in the drug industry or your doctor.
 






Generics Co. Rips Novartis' Bid To Combine Reclast Suits

By Linda Chiem
Law360, New York (May 01, 2013, 2:02 PM ET) -- Wockhardt USA LLC told a New Jersey federal judge Tuesday that three patent infringement suits launched by Novartis Pharmaceuticals Corp. seeking to block drugmakers from developing generic versions of its osteoporosis drug Reclast and oncology drug Zometa should be tried separately.

Wockhardt urged U.S. Magistrate Judge Madeline C. Arleo to reject Novartis' April 12 motion to consolidate the three suits against Wockhardt, Sun Pharmaceutical Industries Ltd., Actavis LLC and Accord Healthcare Inc., saying the cases were at completely different stages of litigation
 






NICE turns town Novartis’ blood cancer drug Jakavi
April 26th 2013

Regulators have refused to recommend the use of Novartis' Jakavi on the NHS in England and Wales to treat patients with certain types of blood cancer.

The National Institute for Health and Care Excellence's (NICE) final draft guidance says Jakavi (ruxolitinib) is not a cost-effective use of NHS resources for the treatment of adult patients with enlarged spleens and related symptoms who have any of the following cancers: primary myelofibrosis, post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis.

Jakavi was approved in the EU in August 2012, but has struggled to prove its worth with the cost-effectiveness body, which has already issued previous draft guidance recommending against the drug's use