Tuesday, December 24, 2013

Insulin pill may soon be a reality

Daily jabs of insulin are a painful reality for many with diabetes. That may change if researchers who have successfully tested oral insulin in rats are able to replicate those results in humans.

Nearly 350m people worldwide suffer from diabetes and that number is predicted to grow to more than 500m by 2030. While the more common form, type-2 diabetes, does not always need insulin treatment, nearly quarter of all diabetes patients depend on insulin jabs. Oral insulin’s estimated annual sales could be somewhere between $8 billion and $17 billion.

The benefits of an insulin pill are more than just ease of taking the drug. The pill will mean that patients can start taking insulin earlier in the development of the disease, which could reduce some of the secondary complications, which can include blindness and impaired healing that leads to amputations.

The idea of oral insulin has been around since the 1930s, but the difficulties of making it seemed too big to overcome. First, insulin is a protein – when it comes in contact with stomach enzymes, it is quickly destroyed. Second, if insulin can pass through the stomach safely, it is too big a molecule (about 30 times the size of aspirin) to be absorbed into the bloodstream, where it needs to be in order to regulate blood-sugar levels.

Sanyog Jain at India’s National Institute of Pharmaceutical Education and Research and his colleagues have been working on delivering insulin in the oral form for many years. Their first fully-successful attempt came in 2012, when they developed a formulation that successfully controlled blood-sugar level in rats. But the materials used were too expensive to consider commercialising the technology.

Now, in a paper published in the journal Biomacromolecules, they have found a cheaper and more reliable way of delivering insulin. They overcome the two main hurdles by, first, packing insulin in tiny sacs made of lipids (fats), and, second, attaching to it folic acid (vitamin B9) to help improve its absorption into the bloodstream.

The lipids they use are cheap and have been successfully employed to deliver other drugs before. These help to protect insulin from being digested by stomach enzymes, which gets it to the small intestine. When the lipid-covered sacs enter the small intestine, special cells on its lining called microfold cells are attracted to the folic acid in them. The folic acid helps activate a transport mechanism that can let big molecules pass through into the blood. The amount of folic acid used in the formulation also seems to be in the safe region.

In rats, Jain’s formulation was as effective as injected insulin, although the relative amounts that entered the blood stream differed. However, it was better in one key aspect. Whereas the effects of an injection are quickly lost (in less than 6 to 8 hours), Jain’s formulation helped control blood-sugar level for more than 18 hours.

The most important part of the research comes after successful testing in animals – the formulation needs to be given to human volunteers. But, Jain said, “at a government institute like ours, we don’t have the sort of money needed for clinical trials.”

He may not have to wait for long, as big pharma companies have been searching for an insulin pill formulation for decades. Two of them, Danish pharma giant Novo Nordisk and Israeli upstart Oramed are in a race to come up with a solution. Google’s venture capital arm, Google Ventures, recently invested $10m in Rani Therapeutics with the hope it will help develop oral insulin. Indian firm Biocon also does oral insulin research, and it recently signed an agreement with pharma giant Bristol-Myers Squibb.

Oramed is ahead, with their oral insulin product soon to enter phase-II clinical trials, which is the most advanced stage any oral insulin formulation has ever reached. Its chief scientist, Miriam Kidron, said of Jain’s research: “Most people have the same basic idea to develop an insulin pill, but its the little differences that will determine ultimate success.”

While Kidron did not reveal Oramed’s formulation, she said, “we attempted liposomal delivery before, just like Jain’s work, but we weren’t successful.” She warned that translating success from rats to humans is very difficult. And she is right – most drugs have a high cull-rate at each stage of their development. Even so, research like Jain’s give hope that an insulin pill may not remain a dream for long.

http://theconversation.com/insulin-pill-may-soon-be-a-reality-21696

IPC urges govt to ensure only registered pharmacists dispense drugs in all chemist shops

The Indian Pharmaceutical Congress (IPC), the largest congregation of pharmacists and pharma professionals, has urged the union health ministry to make sure that registered pharmacists are present and they only dispense drugs in all the chemist shops across the county, thus implementing the laws in uniformity.

The 65th edition of the IPC, which concluded at Amity University, Noida near here on December 22 after three-days of intense deliberations and power-packed scientific sessions, said some states like Maharashtra, Goa and Tamil Nadu had taken the lead in this regard while it was blatantly violated in most of the other states.

“We urge the health ministry to take it up with all the states and agencies to make sure that the chemist shops do have registered pharmacists present all the time, in line with the laws under the Indian Pharmacy Act and the Drugs and Cosmetics Rules,” said the resolution.

Speaking at the valedictory function as the chief guest, union minister for labour and highways Oscar Fernandes supported the demand and said he would take the lead to implement this resolution. “We have the largest network of ESI hospitals and I will see that the ESI hospitals would follow this rule. I will champion your cause,” said the minister who also holds the charge of ESI hospitals.

The minister also pointed out that pharma industry had made the country proud all over the world with its generic strides, especially in therapeutic areas like HIV where India supplies 80 per cent of the drugs to the world.

The resolution also pointed out that even the government dispensaries and even the district hospitals in the public sector did not follow the rules and did not have registered pharmacists. “The rule is only on the paper, and is not followed,” it said.

In another resolution, IPC recommended that the pharmacy education at all levels be brought under a single regulatory control and all powers should be vested with Pharmacy Council of India (PCI). It should have complete authority and accountability to improvise the educational standards at all levels. The dual control by the All India Council for Technical Education (AICTE) and PCI had led to mushrooming of colleges, deteriorating the quality of education, the resolution said.

The third resolution sought an amendment in Rules 71 (1) and 76 (1) under Drugs and Cosmetics Rules 1945 according to which candidates possessing bachelors in pharmacy shall only be considered as expert technical staff in drug manufacturing and analysis.

The three-day event, involving over 4000 delegates from different areas from pharma industry to pharmacy, from academics to research, from sales to quality control, from pharmacovigilance to marketing, saw thought-provoking scientific sessions. As many as 79 speakers led the discourses, spread over symposia, plenary sessions, memorial lectures and panel discussions.

The next edition of the IPC will be held at Hyderabad and the All India Drug Control Officers’ Confederation (AIDCOC) will be the host association, it was announced at the event. The present edition was hosted by Indian Pharmacy Graduates Association (IPGA) and the theme for the conference was “Pharma Vision 2020: Empowering pharmacists”.

One of the major attractions of the meet was the job fair, first time held, for the pharmacy students. Organisers said as many as 20 topline companies interviewed and shortlisted large number of candidates who made a beeline before the pavilion.

The IPC also witnessed a successful Pharmaceutical expo, organized by the Federation of Indian Chambers of Commerce and Industry (FICCI). The expo, focusing on pharma plant and machinery, had nearly 200 exhibitors, including 15 companies from Germany, USA, Korea, Japan, China and Switzerland.

http://www.pharmabiz.com/NewsDetails.aspx?aid=79434&sid=1

Sub-Saharan Africa’s healthcare market to hit $35bn by 2016 – IFC

The healthcare industry is set for huge growth, particularly in Africa, as Sub-Saharan Africa’s healthcare market (including Nigeria) is estimated to hit $35 billion by 2016, according to the International Finance Corporation (IFC) an arm of the World Bank Group report.

In a just released report titled “The Business of Health in Africa” the IFC says that the  growth will increasingly result in massive opportunities for people involved in the healthcare industry and that demand in hospital equipment, medical devices and pharmaceuticals is stepping up.

They add that this will result in better quality health services and improved acces to medicare across the region.

According to the report “Health care provision accounts for half the investment opportunity, with the remainder split across distribution and retail, pharmaceutical and medical product manufacturing, insurance and medical education.

These investments will fund capacity expansion, new businesses and renovation of existing assets.

“About half of these investments are expected to be made by for-profit entities, the remaining portion of private sector being equally spread between social enterprises and non-governmental organisations (NGOs). The vast majority of the investment opportunities in the near term will be the SME sector. Only a quarter of the opportunities are expected to have a project size larger than $3million. Ultimately, the vigour of the private health sector in Sub-Saharan Africa will rely on the commitment, creativity, and integrity of the people of Africa.”

According to the World Health Organisation (WHO)  Africa’s Sub-Saharan region alone accounts for 11 percent of the world’s population yet bears 24 percent of global disease burden and commands less than one percent of global health expenditure.

The growth potentials within  Sub-Saharan Africa healthcare is coming as huge opportunities are in the offing for local drug manufacturers including Fidson Healthcare Plc GlaxoSmithKline, Pfizer Nigeria and East Africa region (NEAR), Evans Medicals, Swipha, and Neimeth Pharmaceuticals, to grow their revenues on the back of recent surge in non-communicable diseases (NCDs).

Lured by an emerging middle class, rising disease burden, especially NCDs such as cardiovascular and respiratory disorders, cancer and diabetes, major pharmaceutical companies are increasingly looking to harness Africa’s opportunity by producing drugs to address these medical conditions.

Although the total size of the African market may seem small, compared to other global regions, analysts believe major big cities within the continent including Lagos, hold the key to unlocking the pharmaceutical industry’s lucrative potential. In these areas, increasing wealth, along with stronger health system infrastructure and rising demand for drugs treating chronic diseases, are driving demand for pharmaceuticals products.

“Urban centres have the highest concentration of the segments of the population that are more likely to be relatively wealthy, more likely to be educated and also possibly more likely to suffer from the chronic diseases of affluence that are becoming increasingly important in Africa,” Sarah Rickwood, director of Thought Leadership at IMS Health told CNN.

An IMS report titled “Africa: A ripe opportunity,” reveal that by 2020, the market could represent a $45 billion opportunity for drug makers, spurred in part by robust economic growth and demographic changes.

While infectious illnesses like HIV/AIDS, malaria, tuberculosis still remain a huge problem, the continent is also projected to experience a surge in demand for treatment of NCDs in the coming years. The WHO estimates that by 2020 the biggest increases in NCD deaths will occur in Africa.

With major market-leading multinationals like Sanofi and GlaxoSmithKline having a strong presence in Africa, diverse drug manufacturers have made significant inroads in recent years. Indian and Chinese companies have more than doubled their imports to Africa over the last decade.

With India being the world’s third largest producer of pharmaceutical products by volume, with an annual turnover estimated at over $20 billion, latest findings by BusinessDay reveal that the value of Indian pharma products exported to Nigeria, stood at $307 million as at March 31, 2012.

As investment in more specialised diagnosis centres relating to cardiovascular and oncological (tumour and cancer-related) diseases has continued to improve the level of patient diagnosis, increasing levels of affordability have spurred demand for prescribed chronic medicines.

While overall projections are optimistic, regulatory delays and continued proliferation of parallel imports and counterfeit products remain a primary market restraint. These restraints are however forecast to have a diminished effect in the long-term, as a result of sustained regulatory reform and improved regulatory efficiency.

Health investors believe the healthcare sector is well placed to take advantage of the expected growth on the African .


http://businessdayonline.com/2013/12/sub-saharan-africas-healthcare-market-to-hit-35bn-by-2016-ifc/

Monday, December 23, 2013

GSK makes sweeping changes to sales incentives

GlaxoSmithKline plc has issued a plan to end direct payments to physicians for promoting its prescription drugs and will no longer pay to have key physicians attend industry conferences.

The new policy also will stop the use of individual sales targets and instead pay its salespeople on the basis of technical knowledge, quality of service and overall business performance, GSK said Tuesday. The plan will be rolled out over the next year and is expected to be in place by early 2015.

At the same time, the company will begin a two-year process to change the way it works with doctors and other healthcare professionals. It will end the "practice of paying them to speak on its behalf, about its products or disease areas, to audiences who can prescribe or influence prescribing."

The U.K.-based big pharma's actions come after the company has received criticism and run into legal troubles for aggressive marketing tactics. An investigation is ongoing in China, where GSK has been accused of bribing travel agencies to boost drug sales.

The company in 2012 reached a $3 billion settlement with the U.S. government over charges that it marketed some drugs off-label, to treat medical conditions for which they had not received approval by the Food and Drug Administration.
GSK chairman Andrew Witty insists the latest change in sales incentives is not related to the Chinese bribery scandal or off-label charges, but that it is another step in the company's attempts to make its actions transparent.

"We recognize that we have an important role to play in providing doctors with information about our medicines, but this must be done clearly, transparently and without any perception of conflict of interest," Witty said in a same-day statement.

The changes are unlikely to make a difference in smaller companies' choice of GSK as a collaboration partner; observers expect other pharmaceutical companies to take steps in the same direction as the industry has faced scrutiny in recent years.

GSK already took a similar tack with its U.S. sales operations in 2011, using a program it called "Patient First."

PhRMA, the U.S. pharmaceutical trade group, changed its code of conduct in 2009 to require stricter limits on the use of physicians as marketing tools. AstraZeneca plc made a decision along those lines as well in 2011.

Under the Physician Payment Sunshine Act, contained within the Affordable Care Act, pharma companies must develop a transparency program, which the Centers for Medicare and Medicaid Services calls "Open Payments." Drug makers must report to CMS any payments or other transfers of value to physicians and teaching hospitals. The data are collected annually and published on a public website. The collection began in August.

In a related matter, the U.S. Supreme Court on Monday let stay a lower court ruling in the case of Scott Harkonen, former CEO of InterMune Inc. Harkonen had been convicted of wire fraud by misrepresenting the results of a clinical trial for the drug Actimmune to shareholders. Harkonen had appealed citing free speech, but now his earlier conviction stands. As a result, he cannot work for any company that bills Medicare. InterMune also ended up paying $36 million to settle Justice Department allegations of off-label marketing in the incident.


Read more: GSK makes sweeping changes to sales incentives - The Deal Pipeline (SAMPLE CONTENT: NEED AN ID?) http://www.thedeal.com/content/restructuring/gsk-makes-sweeping-changes-to-sales-incentives.php#ixzz2nrQ4KN00


Biocon inks licensing pact with Quark Pharma

Biotechnology major  Biocon today said it has inked a pact with Quark Pharmaceuticals, to develop a range of siRNA (small interfering RNA)-based novel therapeutics.

The companies have entered into a licensing and collaboration agreement for the development of a range of siRNA-based novel therapeutics, Biocon said in a statement.

“This collaboration will enable Biocon to co-develop, manufacture and commercialise QPI-1007, a novel siRNA drug candidate for ophthalmic conditions, for India and other key markets,” it added. As part of the agreement, Biocon will have access to Quark’s innovative and proprietary siRNA technology platform that can be leveraged for the development of novel therapeutics for various unmet medical needs.

 The company, however, did not disclose financial details. Commenting on the development, Biocon Chairperson and Managing Director Kiran Mazumdar Shaw said Quark is the world leader in this technology and their joint development efforts on QPI-1007, targeting ocular neuroprotection, aims at providing relief to several patients suffering from serious ophthalmic conditions.

 “This collaboration reinforces our commitment to develop and introduce innovative therapeutics to India to meet the unmet medical needs. We hope to use this technology for developing several other novel therapeutics,” she added. QuarkPharma CEO Daniel Zurr said the collaboration will position Biocon as the leading siRNA company in India and as an international player in this new drug category.

 Biocon shares closed at Rs 437.35, up 11.38 percent, on the BSE on Wednesday. Biocon stock price On December 18, 2013, Biocon closed at Rs 437.35, up Rs 44.70, or 11.38 percent. The 52-week high of the share was Rs 450.90 and the 52-week low was Rs 255.00.

 The company's trailing 12-month (TTM) EPS was at Rs 15.02 per share as per the quarter ended September 2013. The stock's price-to-earnings (P/E) ratio was 29.12.

 The latest book value of the company is Rs 110.34 per share. At current value, the price-to-book value of the company is 3.96.

Read more at: http://www.moneycontrol.com/news/business/biocon-inks-licensing-pactquark-pharma_1010463.html?utm_source=ref_article

ICMR to approve formation of clinical researchers’ network to strengthen capacity building of experts

Indian Council of Medical Research (ICMR) may soon approve formation of a network of representatives from the clinical research fraternity in the country. These could include experts from medical colleges, pharmacy colleges, government medical centres, private hospitals and research centres across the country. This network of professionals could be engaged in providing the required support and assistance for the conduct of drug monitoring  and human studies in country.

The move is expected to bolster efforts to register the disease registries in the country to be able to get a direction on the kind of novel drugs required in the country to tackle some of the infectious diseases.

The Council has assessed the shortfall of experts over the growing number of drugs available for any disease or disorder. Therefore, it is looking to ensure a system in place with the formation of a network of representatives. The working committees and expert groups are already formed to put in place a network of clinical research representatives.

“We have sent in a proposal to our parent body, ICMR, for the creation of a network of representatives from the clinical research space,” said Dr Nilima Kshirsagar, National Chair (Clinical Pharmacology), Indian Council of Medical Research, dean, ESI-PGIMSR MGM Hospital.

Dr Kshirsagar who was in Bengaluru for the IPSCON 2013 stated that the network of clinical research representatives identified by ICMR would look to partner with the Medical Council of India and the Department of Health Research. This would be the first effort to capacity building of human resources in the sector of clinical research and pharmacovigilance.

“India needs policy action and evaluation of the current protocols in the area of clinical research. There is need for studies with old generic drugs, evaluation of risks and cost availability benefits with the existing medicines. The lacunae  is that despite some of the excellent research centres, the country lacks the representative data of drug studies on humans. This has seen the delay in the regulatory approvals. If the necessary drug references are made accessible, it would also be easy for drug regulators to speed up clearances,” she added.

Now the key benefit of the network of representatives is that  it could provide the required efficiency and transparency in having a better understanding of a disease and plan for research. It could help the country to maintain a database of drugs in the market and in the pipeline. The big benefit would be to the regulatory authority in helping take faster decisions on the submitted application for dug clearances by the pharma industry, she noted.

http://www.pharmabiz.com/NewsDetails.aspx?aid=79415&sid=1

China Biotech Week In Review: Simcere Pharma Going Private

Chengdu Kanghong Pharmaceutical Group was granted CFDA approval for conbercept, a novel treatment for wet age-related macular degeneration. The drug is the first innovative, China-developed monoclonal antibody to gain regulatory approval, a significant milestone. The company believes its drug offers significant advantages over similar existing western MAbs.

MicuRx Pharmaceuticals, a San Francisco-Shanghai company focused on antibiotics, will start a China Phase II trial of its next-gen oxazolidinone antibiotic. The trial will enroll 200 patients with complicated skin and skin structure infections. MRX-I was developed to treat drug-resistant Gram-positive infections. The China trial is part of a larger global development program for MRX-I: the company is also starting a Phase I bridging study in Australia in a non-Chinese population.

Deals and Financings

Alvogen, a multinational maker of complex generic drugs, will buy 67% of Taiwan's Lotus Pharmaceutical for $210 million. Lotus makes generic oral and injection drugs in a wide variety of therapeutic areas. Lotus will manufacture Alvogen drugs, which will be sold in China and the rest of Asia, while, reciprocally, Alvogen will help Lotus obtain US approval for its products.

Hutchison China MediTech (Chi-Med) will form a drug distribution JV with Sinopharm (HK: 1099), investing $9.8 million to buy majority control (51%) of a Sinopharm subsidiary, HuYong Pharmaceutical (Shanghai). Chi-Med intends to use the JV to distribute its own drug products and to provide distribution/marketing services to other pharmas.

Simcere Pharma (NYSE: SCR) will go private, the last in a line of US-listed China pharmas to regain private-company status (see story). Shareholders voted overwhelmingly in favor of a deal that values the company at $506 million. A consortium led by the company's chairman and founder, Jinsheng Ren, offered $9.66 per ADS ($4.83 per ordinary share) last March. As a private company, Simcere will probably not be as inclined to report the progress of its innovative partnerships, a loss for those of us outside the company.

http://seekingalpha.com/article/1911081-china-biotech-week-in-review-simcere-pharma-going-private?source=google_news

Pharma in good health, but shift to cyclicals will hurt

The BSE healthcare index outperformed the broader market indices in 2013, as was the case in 2010, 2011 and 2012.

This was on the back of issues such as subdued domestic growth on the back of implementation of NLEM 2011 and the tussle between distributors and retailers over trade margins coupled with an increased scrutiny and scores of warning letters from the USFDA which undid the robust growth on the back of stronger US traction.

On the domestic front, the current sluggish trend is likely to accelerate to 8-10 per cent growth in CY14 (on a lower base) driven by mid-teens growth in chronic therapies such as anti-dietetic, cardiology, neurology, etc. On the flip side, we expect some of the acute therapies like anti-infectives, gastro-intestinal and respiratory to continue to post flat to marginal growth.

On the exports front, we expect 15-20 per cent growth in dollar terms, as most players have developed a rich product pipelines over the past three or four years. Despite the passage of generic GDUFA, the pace of product approvals has not improved in CY13. Issues such as delay in approvals are likely to improve in CY14. We expect incremental approvals from the USFDA, going ahead

In CY13, product approvals from key emerging markets like Brazil, Russia, South Africa, Mexico and Turkey also witnessed delays due to events such as strikes at some of the regulatory offices (Brazilian ANVISA) and changes in registration process by some counties. We expect product approvals to normalise from these countries in CY14

To conclude, we expect buying interest to sustain as most players are likely to maintain the growth tempo based on manufacturing fungibility, geographical diversification, product appro­vals/pipeline and, hence, clear visibility. We do not envisage the US tapering having any impact on sector preference. However, we expect some impact depending on the election outcome as the new government is likely to put reforms on the fast track, hence, shifting buying preference towards cyclicals

Among key risks are FDA hurdles, pricing pressure in the US as well as various emerging markets.

Of late, the USFDA has adopted a zero-tolerance policy for adherence to GMP practices with more randomised scrutiny, which does not necessarily follow a set pattern. A recent flurry of import alerts and warning letters to domestic companies is a result of that.

 Consolidation of generic sourcing agencies (pharmacy chains) in the US is likely to put pressure on pricing in the US, especially for players that do not have a direct presence in the US (recent JV- CVS Caremark and Cardinal Health) Pricing pressure imposed by other emerging economies to arrest the spiralling healthcare cost is also likely to be the limiting factor Out top picks in the space include Lupin, Sun Pharma, Ipca Lab and Glenmark Pharmaceuticals.



http://www.mydigitalfc.com/sectoral-watch/pharma-good-health-shift-cyclicals-will-hurt-024

Friday, December 20, 2013

Biocon's New Job Application Portal | Latest jobs at Biocon, Bangalore

Recruitment has always been a tough task especially for bigger companies of the stature of Biocon. Given that they receieve large volumes of Resume's and application for every Job they post.

Many companies outsource this recruitment portal to American companies such as webshire, Taleo etc. However Our Very own Biocon has opted to create its own Recruitment management system Here

Given the fact that Obtaining Quality Human resource is a tough task for Biotech industry, These Recruiment management Systems will certainly Help Biocon overcome this uphill task of managing the thousands of resume's they receive each day.

Biocon has always been at the forefront whether its promoting Biotech education or creating a platform where industry & Academia can interact. Recently we had an announcement where in the company had partenered with Government of Karnataka to Develop finishing Schools for the upliftment of Biotech eucation in the state.

We wish Dr Shaw and their entire Human Resource department all the best in this latest endeavour of developing a separate portal for Job seekers.

http://www.biotecnika.org/news/may-2011/biocons-new-job-application-portal-latest-jobs-biocon-bangalore

Thursday, December 19, 2013

Partnering Deals and Alliances with Big Pharma 7th Edition

The Partnering Deals and Alliances with Big Pharma report provides the most comprehensive and in-depth insight into the dealmaking interests and activity of the worlds leading fifty big pharma companies.

Partnering Deals and Alliances with Big Pharma provides the user with the following key benefits:
Detailed partnering activity profiles for each of the top 50 big pharma companies
Over 300 charts showing a company's dealmaking activity since 2007, allowing quick identification potential partners

Partnering therapy focus revealed

Partnering activity since 2007 - number of deals per year

Full listing of partnering deals

Activity by deal type

Activity by industry sector

Activity by phase of development

Activity by technology type

Activity by therapeutic area

Comprehensive access to over 3,000 partnering deals as recorded at Current Agreement, together with contract documents if available

Insight into the terms included in a partnering agreement, together with real world clause examples, via contract documents

Understand the key deal terms the company has agreed in previous deals

Undertake due diligence to assess suitability of your proposed deal terms for partner companies
The Partnering Deals and Alliances with Big Pharma report provides the most comprehensive and in-depth insight into the dealmaking interests and activity of the worlds leading fifty big pharma companies.

This premier report provides all the information you require to better understand big pharma partnering.

One of the key aspects of partnering is finding those companies that are potential candidates for the development and commercialization of the next generation of therapies.

 A lot of resources are spent on finding partners, identifying their interests and making contact to initiate discussions.

Using this report, dealmakers will effectively and efficiently target their partnering activities to deliver the company's business development objectives. Over 300 charts allow quick understanding of each big pharma companies dealmaking trends over the last four years.

This report contains over 3,000 links to online copies of actual partnering deals as recorded at Current Agreement, together with contract documents if submitted to the Securities Exchange Commission by bigpharma and their partners.

Contract documents provide the answers to numerous questions about a prospective partner's flexibility on a wide range of important issues, many of which will have a significant impact on each party's ability to derive value from the deal.

http://www.sys-con.com/node/2903412

Monday, December 16, 2013

Lundbeck and Otsuka to co-develop Lu AF20513, an investigational vaccine against Alzheimer's disease

. Lundbeck A/S (Lundbeck) and Otsuka Pharmaceutical Co., Ltd. (Otsuka) have announced that they will further expand their collaboration to include the development of Lu AF20513, an investigational vaccine candidate against Alzheimer's disease.
Lu AF20513 is an active anti-Aβ vaccine candidate against Alzheimer's disease which currently is in preclinical development. It is designed towards an optimal immunogenic response in the elderly, based on the hypothesis that cognitive function would be preserved through the early inhibition of amyloid beta depositions.

The agreement covers the development of Lu AF20513 through clinical phase I. Following completion of the clinical phase I study the parties have an option to enter into a co-commercialisation and co-development agreement under terms to be agreed upon.

Lundbeck will receive from Otsuka an initial payment of EUR 4 million (approximately DKK 30 million) upon signing and Lundbeck will finance the phase I development costs. Additional specific financial terms of the agreement remain undisclosed.

It is expected that the phase I study will be initiated during 2014.

In addition to the vaccine candidate Lu AF20513, the two companies are pursuing the clinical development of two other potential treatments for different symptoms that can occur in patients with Alzheimer's disease - Lu AE58054, a 5HT6 receptor antagonist for adjunctive treatment of Alzheimer's disease and brexpiprazole, an investigational agent with high affinity to multiple serotonin, dopamine and norepinephrine receptors for the treatment of agitation in patients with Alzheimer's disease. Both projects are currently in clinical phase III.

These programs illustrate the depth and breadth of experience and resources the two firms can draw on in neuroscience research and development. The two companies' collective revenues in the central nervous system (CNS) area rank the alliance number one in this field.(1)

About Lu AF20513
Lu AF20513 is an active vaccine inducing high affinity polyclonal antibodies that target beta-amyloid (Aβ), a protein that can exert toxic effects in the brain and is believed to play a central role in the pathology of Alzheimer’s disease. Lu AF20513 is expected to provide an enhanced and heterogeneous immunogenic response towards Aβ peptides in comparison to mono-clonal antibody treatment strategies.

About Alzheimer's disease
Alzheimer's disease is a progressive brain disorder in which the brain gradually degenerates. It most frequently occurs in people above 65 years of age. People with Alzheimer's disease develop distressing changes in memory, thought, function and behaviour, which worsen over time. These changes increasingly impact the person's daily life and reduce their independence until ultimately these patients are entirely dependent on others.(2)

Alzheimer's disease also has an enormous impact on the patient's caregiver. Most caregivers are close relatives who provide care at home - a demanding and exhausting role that represents a significant emotional and physical burden.(3)

Worldwide, it is estimated that about 44 million people have dementia. With the shift towards an increasingly elderly population, it is predicted that the number of people affected by dementia will almost double every 20 years, and by the year 2050, 135 million people will have the condition.(4) Alzheimer's disease is the most common cause of dementia, accounting for 50 to 80% of these patients.(5)

The worldwide costs of dementia (estimated at around USD 600 billion in 2010) amount to more than 1% of the global gross domestic product (GDP).

About Lundbeck
H. Lundbeck A/S (LUN.CO, LUN DC, HLUYY) is a global pharmaceutical company specialized in brain diseases. For more than 50 years, we have been at the forefront of research within neuroscience. Our development and distribution of pioneering treatments continues to make a difference to people living with brain diseases. Our key areas of focus are alcohol dependence, Alzheimer's disease, depression/anxiety, epilepsy, Huntington’s disease, Parkinson's disease, schizophrenia and stroke.

Our 5,800 employees in 57 countries are engaged in the entire value chain throughout research, development, production, marketing and sales, and are committed to improving the quality of life of people living with brain diseases. Our pipeline consists of several late-stage development programs and our products are available in more 100 countries. We have research centers in China, Denmark and the United States, and production facilities in China, Denmark, France, Italy and Mexico. Lundbeck generated revenue of approximately DKK 15 billion in 2012 (EUR 2 billion; USD 2.6 billion).

Lundbeck's shares are listed on the stock exchange in Copenhagen under the symbol "LUN". Lundbeck has a sponsored Level 1 ADR program listed in the US (OTC) under the symbol "HLUYY".

About Otsuka Pharmaceutical Co., Ltd.
Otsuka Pharmaceutical Co., Ltd. is a global healthcare company with the corporate philosophy: 'Otsuka-people creating new products for better health worldwide.' Otsuka researches, develops, manufactures and markets innovative and original products, with a focus on pharmaceutical products for the treatment of diseases and nutraceutical products for the maintenance of everyday health.

In pharmaceuticals, Otsuka is a leading firm in the challenging area of mental health and also has research programs for several under-addressed diseases including tuberculosis, a significant global public health issue. These commitments illustrate more powerfully than words how Otsuka is a "big venture" company at heart, applying a youthful spirit of creativity in everything it does.

Otsuka is a wholly owned subsidiary of Otsuka Holdings Co., Ltd., the holding company for the Otsuka Group. The chairman Akihiko Otsuka is the third generation of Otsuka family members to lead the business, whose origins date from 1921. The Otsuka Group employs approximately 42,000 people globally and its products are available in more than 80 countries worldwide. Consolidated sales were approximately EUR 10 billion or USD 13 billion for fiscal year 2012 (4/1/2012-3/31/2013).

1. Based on IMS data (MATQ2.2013)
2. Georges J, Jansen S, Jackson J, et al. Alzheimer's disease in real life - the dementia carer's survey. International Journal Geriatric Psychiatry 2008; 23 (5): 546—551.
3. Mohamed S. et al. Am J Geriatr Psychiatry. 2010 Oct;18(10):917-27 and Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE)-AD study
4. Alzheimer's Disease International. The global impact of dementia 2013-2050; 2013.
5. Alzheimer's Association. "Alzheimer's changes the whole brain" Brain Tour. 2011. Document accessible at: http://www.alz.org/braintour/alzheimers_changes.asp.

http://www.worldpharmanews.com/lundbeck/2652-lundbeck-and-otsuka-to-co-develop-lu-af20513-an-investigational-vaccine-against-alzheimers-disease

Saturday, December 14, 2013

Flu vaccinations cut risk of pneumonia hospitalizations by almost 60%, study finds

Influenza vaccination can reduce the risk of influenza-associated pneumonia hospitalizations by more than half, according to data presented at the recent IDWeek Meeting in San Francisco.

Using a case test-negative study design, Carlos G. Grijalva, MD, MPH, of Vanderbilt University School of Medicine, Nashville, Tenn., and researchers found that influenza vaccination was associated with a 59% reduction in the risk of laboratory-confirmed, influenza-associated pneumonia hospitalizations.

“The vaccine effectiveness appeared to be higher among children than among adults,” said Grijalva, assistant professor of health policy, preventive medicine, division of pharmacoepidemiology, department of health policy. “Several studies have shown that influenza vaccines can prevent acute respiratory diseases associated with influenza infections, but evidence of protection against other more severe outcomes, such as hospitalizations for influenza-associated pneumonia, is limited.”

The study

The finding comes from the CDC's Etiology of Pneumonia in the Community (EPIC) study covering two flu seasons — 2010 to 2011 and 2011 to 2012 — and part of a third, 2009 to 2010, in the cities of Memphis, Nashville, Chicago, and Salt Lake City.

The influenza vaccine effectiveness study included 2,320 children and adults hospitalized with pneumonia and enrolled in the EPIC study. The analyses compared influenza vaccination between patients hospitalized with laboratory-confirmed influenza pneumonia and patients hospitalized with pneumonia who tested negative for influenza.

Vaccination information for the study was verified through review of medical records, vaccination registries, and information from other providers (e.g., pharmacies).

Among study subjects, 130 had laboratory-confirmed influenza, Grijalva said. He and colleagues used regression analyses to determine the adjusted odds ratio (aOR) for influenza vaccination more than 14 days before disease onset in cases compared with non-cases. From that, they calculated vaccine efficacy as 1-aOR.

Of the 130 cases, 22% had influenza vaccination for the current season, compared with 35% of the non-cases. That yielded a vaccine efficacy of 59%, which did not vary substantially in sensitivity analyses, although there was some variation in subgroups. In particular, vaccine effectiveness was 79% in children but only 36% in adults.

“Most previous studies on this subject focused on all-cause pneumonia as the outcome but lacked laboratory confirmation of influenza infections, and several studies lacked verification of the vaccination status,” Grijalva said. “We designed this study to determine whether influenza vaccination reduced the risk of laboratory-confirmed, influenza-associated pneumonia hospitalizations in individuals ≥6 months of age with verified influenza vaccination information.”

Currently, the Advisory Committee on Immunization Practices recommends influenza vaccination for all eligible individuals six months of age or older. “Our study provides additional support to these recommendations, indicating that influenza vaccination can provide protection against influenza-related pneumonia hospitalizations,” Grijalva said.

- See more at: http://drugtopics.modernmedicine.com/drug-topics/news/flu-vaccinations-cut-risk-pneumonia-hospitalizations-almost-60-study-finds#sthash.5uraWM2H.dpuf

The pharmacist’s role in medication reconciliation

Gathering an accurate medication history for hospital patients is definitely a team effort shared by pharmacists, physicians, and nurses. To be successful, somebody has to take ownership of the process to monitor the medication reconciliation. The pharmacist must champion this process for it to work smoothly.

In the hospital

Hospitalists, attending physicians, medical residents, and interns all recognize how important it is to collect an accurate medication history and ensure precise medication reconciliation.

Hospitals should develop a clearly defined workflow for pharmacists and physicians to obtain and reconcile medication histories. Medication reconciliation, effectively conducted, will provide an accurate discharge medication list.

The electronic medical record system will maintain the medication histories; if patients are readmitted, this information will be readily available to the emergency department. However, the record must be reviewed and updated by clinicians.

In the community

The pharmacist in the community setting, whether it be in a chain store, an independent pharmacy, a big-box operation, a supermarket, or a hospital ambulatory care apothecary, will become involved in this process as well.

The hospital’s clinical pharmacist may rely on the community pharmacist for an accurate and updated list of the medications currently prescribed to the patient. In most cases, the primary care physician has an accurate record of the patient’s medications and will provide the patient with a printout, using the NextGen program. It is imperative for the patient to carry this list with him or her at all times — especially when being treated by a specialist or an emergency department clinician.

It is then up to the attending physician to determine which home medications the inpatient will continue taking while admitted, and which, if any, should be changed upon discharge.

Three types of meds

There are three major categories of medications that an inpatient can be prescribed during the admission process.
  •     Ÿ The first group comprises the medications used to treat the symptoms that occasioned the admission. If a patient is admitted for bronchial pneumonia, he or she is usually given aggressive intravenous antibiotic therapy. If a patient presents with septic shock, therapy with vasopressors is usually initiated.
  •     Ÿ The second group of medications includes those employed to prevent adverse events, such as heparin or enoxaparin used for prophylaxis against a DVT. Low-dose aspirin also falls into this category. Notice that heparin, norepinephrine, and vancomyin are not included in the patient’s home medication reconciliation list.
  •     Ÿ The third category of medications prescribed for the inpatient includes the home medications. This is the list of medications that the patient takes on a daily basis. It should be provided to the emergency department physician upon admission to the hospital.

The attending physician or hospitalist will then determine which of these medications should continue and which should be stopped while the patient is a hospital inpatient. If intravenous metoprolol is prescribed, the physician might want to discontinue the patient’s PO carvedilol to prevent duplication of therapy. PO OxyContin and all combinations may be discontinued while the patient is being given IV morphine following a surgical procedure.

Teaching hospital

When pharmacists, retail or hospital, work in tandem with medical residents in a community teaching hospital, the collaboration should lead to a reduction in readmissions, emergency department visits, and hospital costs.

Complete and accurate medication reconciliation by the entire healthcare team will increase overall accuracy of the admission process.

- See more at: http://drugtopics.modernmedicine.com/drug-topics/news/pharmacist-s-role-medication-reconciliation#sthash.hLYDZXlj.dpuf