by JoelLane
23. May 2012 15:13
Most high-level medical customers think biopharmaceutical companies should take more commercial risks, according to a new survey.
The New Health Report 2012 from Quintiles also noted that a majority of pharma executives and their customers support more risk sharing in commercial deals.
It also found that 81% of UK patients with long-term conditions would be willing to accept greater clinical risks for the sake of greater benefits.
The report was based on a survey of more than 1350 biopharmaceutical and healthcare management executives and healthcare investors in the US and the UK.
Better metrics are needed to assess both commercial and clinical risks for the sake of wider consensus, the report concluded.
More than half of NHS executives thought the pharma industry was too risk-averse, while 65% of industry executives thought their companies too enough or too many risks.
However, there was widespread agreement between companies and customers on the value of risk-sharing agreements, with 73% of NHS executives and 55% of industry executives convinced they would promote innovation.
More than 70% of biopharma executives and UK payers also believed innovation would benefit from pre-competitive agreements between companies.
John Doyle, Managing Director of Consulting at Quintiles, commented: “Payers’ interest in early involvement in the drug development process, complemented by their experience in balancing risk and benefit, could serve as a wake-up call to the biopharmaceutical industry.”
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Tags: biopharmaceutical industry, biopharmaceutical companies, New Health Report 2012, Quintiles, NHS payers, NHS customers, commercial risks, clinical risks, risk sharing, innovation, John Doyle
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by emma
8. November 2011 14:02
The Government needs to do more to support life sciences in the UK and create an environment where the industry can flourish, a new survey has found.
RSA’s The UK Life Sciences Leaders’ Survey 2011 revealed worries over the NHS reforms, medicine pricing and reimbursement, employment issues and the cost of research amongst its leaders.
Nick Stephens, CEO of RSA, says the Government “urgently needs to do more to ensure that education, regulation, access to medicines and the NHS research base align to support the industry’s continued contribution to the UK economy”.
The report is the second annual survey of industry bosses. Last year the general feeling was of optimism with leaders believing the recently elected coalition Government would improve the business environment.
But twelve months later the mood has changed with results finding leaders claim the UK is not competing effectively globally, creating opportunities for early phase/smaller companies or making the most of its unique selling points: the NHS and skills in innovation and discovery.
Leaders also raised concerns about the increasing cost of working in the UK, the implication of R&D as a result of the NHS reforms, the regulatory burden on operations and the process from development to market. They also advised that fiscal and tax incentives should be given to SMEs to help their growth and the UK compete globally.
Worries were also raised about the introduction of value-based pricing. However, in contrast, health technology assessments were broadly welcomed as a means of enhancing value and meeting therapeutic requirements, the report found.
During the tough economic environment, the survey found that leaders would focus on innovation, creating flexible organisations and processes, and refocusing research and development to weather the current storm.
In a perfect world, leaders revealed they would investing in R&D and make the healthcare sector, regulatory and commercial environment work closer together to achieve better outcomes for patients and the pharmaceutical industry.
Stephen Whitehead, CEO, ABPI, says the survey shows more support is needed for biopharmaceutical companies in the ever-changing NHS. “There is much that the Government has done to support the industry, particularly through the Growth Review and the Office for Life Sciences,” he said. “But we need to build on this as part of a continuing relationship with NHS and Government to explore how unnecessary bureaucracy can be eliminated from the healthcare system so that new treatments can reach patients as quickly as possible.”
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Tags: survey, life science, government, life sciences, UK, industry, RSA, UK life Sciences, leaders survey, NHS, NHS reforms, reforms, medicine, pricing, reimbursement, employment, research, leaders, Nick Stephens, CEO, education, regulation, NHS research, UK economy, economy, annual survey, industry bosses, optimism, coalition government, business environment, business, companies, skills, innovation, discovery, r&D, r and d, research and development, market, tax incentives, SMEs, growth, global, worries, value based pricing, health technology, health, therapy, treatment, healthcare, healthcare sector, commercial, regulatory, patients, pharma, pharmaceuticals, pharmaceutical industry, Stephen Whitehead, ABPI, biopharma, biopharmaceutical, biopharmaceutical companies, healthcare system
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by emma
27. September 2011 16:10
The CHMP has recommended Astellas Pharma and Optimer Pharmaceuticals’ Dificlir (fidaxomicin) to treat adults with colon disease.
The drug specifically targets the bacteria causing the infection in the colon whilst avoiding ‘friendly’ bacteria in the gut of patients with the disease, which is also known as Clostridium difficile-associated diarrhoea (CDAD).
Ken Jones, President and CEO of Astellas Pharma Europe, said: “European patients with this potentially fatal disease can take encouragement from the positive CHMP opinion for Dificlir that a new medication for clostridium difficile infection may soon be available.”
Dificlir’s active substance is fidaxomicin, which belongs to the macrocyclic class of antibacterials and inhibits RNA synthesis by bacterial RNA polymerase.
Dr Xavier Luria, Head of Safety and Efficacy at the EMA, said: “This is a promising step forward in the Agency's drive for addressing patients' needs in infectious diseases.”
The positive opinion is based on Phase III clinical research data comparing fidaxomicin with oral vancomycin on patients in the US and Canada. Results of the studies showed that clinical cure was achieved at the end of ten days of treatment with both treatments. Furthermore, fidaxomicin had a significantly lower rate of recurrence of CDI compared to vancomycin.
Dificlir, known as Dificid in the US, was approved by the FDA in May for the treatment of CDAD in adults.
The European Commission will deliver its final decision within three months.
CDI is a serious illness resulting from infection of the internal lining of the colon by C. difficile bacteria. The bacteria produce toxins that cause inflammation of the colon, diarrhoea and, in some cases, death.
UK-based Astellas Pharma Europe manufactures and distributes pharmaceuticals globally with the intention to improve lives through the introduction of innovative and reliable pharmaceutical products.
Optimer Pharmaceuticals, is a biopharmaceutical company focused on developing and commercialising hospital specialty products to treat serious infections and address unmet medical needs.
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Tags: colon disease, CHMP, recommend, recommendation, Astellas Pharma, Optimer Pharmaceuticals, Dificlir, fidaxomicin, pharma, pharmaceuticals, drugs, medicine, medication, treatment, therapy, prescriptions, CDAD, patients, patient care, health, healthcare, health news, Ken Jones, President, CEO, Europe, Clostridium difficile, diarrhoea, macrocyclic, antibacterial, RNA synthesis, Xavier Luria, EMA, safety, efficacy, infectious disease, clinical research, clinical trial, medical, medical research, USA, Canada, vancomycin, EU, Dificid, EC, European Commission, UK, biopharma, biopharmaceuticals, company, biopharmaceutical companies, pharmaceutical companies, business, industry, sector, medical sales
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