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Pharmaceutical Pricing, Reimbursement, and Prescribing News in the Second Quarter of 2007
Decision Resources, Inc., Sep 2007, Pages: 31
Following considerable political activity in drug pricing and reimbursement in the world’s major pharmaceutical markets in the first three months of 2007, the second quarter of the year proved to be relatively quiet. In the United States, Medicare Part D’s growing share of the U.S. prescription drug market could be bad news for pharmaceutical companies because employer-sponsored health plans typically offer more generous drug benefit designs. The French government’s pharmaceutical cost-containment strategies—particularly its vigorous promotion of generics—yielded significant savings. German physicians, pharmacists, and patients struggled to adjust to new manufacturer rebate contracts in the generics market. In Italy, a government-imposed price cut reduced pharmaceutical spending in the first four months of 2007. Spain’s new reference pricing system immediately boosted reference-priced drugs’ share of the pharmaceutical market. In the United Kingdom, a Parliamentary inquiry into the activity of the National Institute for Health and Clinical Excellence (NICE) uncovered serious concerns among drug manufacturers about the institute’s impact on the heath care system domestically and abroad. Following the Japanese government’s announcement that it was considering an overhaul of its drug pricing and reimbursement system in fiscal year 2008, the pharmaceutical industry prepared its proposals for reform.
Get the Answers You Need to Shape Your Strategy
- According to Wolters Kluwer Health, 4.2 million U.S. Medicare beneficiaries—32% of all beneficiaries who had standard eligibility for coverage—fell into the Medicare coverage “gap” in 2006. What is the current trend in the number of health care plans offering coverage of drugs in the gap?
- In June 2007, the U.S. Senate passed the Biologics Price Competition and Innovation Act. This act would afford manufacturers of innovative biologics 12 years of market exclusivity from the time of licensing and would create a procedure for the FDA to approve biosimilar agents that are interchangeable with marketed products. What is the likelihood that the U.S. Congress will pass the bill, and what concerns about the bill has the Bush administration expressed?
- The first rebate contracts between statutory health insurance funds and generics manufacturers in Germany took effect on April 1, 2007. By the beginning of June, 244 statutory health insurance funds had signed such contracts for almost 16,000 different product presentations of off-patent compounds. What challenges has the new system introduced for physicians, pharmacists, and patients? Why are small generics companies being particularly hurt by the new contracts?
- Far from being content with the recent vigorous growth in the French generics market, the French government continues to set aggressive targets for generics dispensing. What is the overall generics dispensing rate the government has targeted for December 2007? Is this target attainable?
- In May 2007, the U.K. House of Commons Select Committee on Health published written submissions it had received from interested parties regarding its inquiry into the activities of the National Institute for Health and Clinical Excellence (NICE). What criticisms and concerns did the pharmaceutical industry express about NICE? What specific recommendations did Bristol-Myers Squibb offer regarding factors NICE should take into account during its drug appraisal process?
- In June 2007, Janssen-Cilag offered the U.K. National Health Service a groundbreaking “moneyback guarantee” for coverage of Velcade. Industry observers believe that the NHS and other health care systems around the world may in future exert pressure on other manufacturers to sign similar risk-sharing agreements for high-priced drugs. What are the preliminary terms of the Velcade agreement? What terms have yet to be worked out?
Scope
- United States: Medicare Part D’s growing share of prescription benefi ts; setbacks for government price negotiations for Medicare Part D; change in PDPs’ coverage in the Medicare gap; relaxation of formulary requirements; new employer-sponsored health plans for early retirees; Congressional debate on the Biologics Price Competition and Innovation Act; the U.S. judiciary’s ruling on the Plavix patent dispute; convictions of Astra-Zeneca, Bristol-Myers Squibb, and Schering-Plough on overcharging.
- European Union: Second Progress Report from the High-Level Pharmaceutical Forum; recommendations from the working group on the relative effectiveness of medicines.
- France: Slowdown in the French pharmaceutical market; the French government’s new costcontainment drive.
- Germany: Introduction of health economic evaluation for some new drugs; increasing demand for copayment-exempt medicines; implementation of a new system of rebate contracts between statutory health insurance funds and generics manufacturers; physician views on cost-containment; survey results regarding the underuse of medicines in the German health care system.
- Italy: Effect of the October 2006 price cuts on growth in the Italian pharmaceutical market.
- Spain: Effects of Spain’s new reference pricing system; the Spanish generics market; accelerated reimbursement decision making at the Spanish Ministry of Health.
- Great Britain: Industry submissions regarding the House of Commons’ review of NICE; the National Audit Office’s review of primary care prescribing costs; NICE’s preliminary support of Janssen-Cilag’s “money-back guarantee” for Velcade.
- Japan: Proposals for reform of the pricing and reimbursement system; the potential for growth in the Japanese
generics market.
- Outlook: Overall U.S. prescription sales in the face of rapid increase in Medicare pharmaceutical spending; opportunities and challenges in the face of employers’ increasing use of value-based health benefit designs; implications for pharmaceutical manufacturers and drug prices of the European Union’s High-Level Pharmaceutical Forum; intensification of reference prices in Germany, Spain, and France; growth of the generics market in France, Spain, and Japan.
Also available
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