Empathy lethal drugs on transnational pharmaceutical companies - multinational, pharmaceutical companies - pharmaceutical industry
The past 10 years, a number of key therapeutic areas to the multinational pharmaceutical industry giants bring huge profits. However, ten years, Hexi east of the river, as the business environment changes, they are giving up these areas of research and development activities, move on to more profitable diseases such as cancer and anti-dementia drug treatment. It also can adapt to growing risk aversion of regulators.
Recently, Eli Lilly, Abbott, Wyeth and Pfizer and other companies have announced a cut of "primary health care drugs," the R & D investment, these drugs are mainly used to treat everything from coughs Cold To heart disease and diseases like high cholesterol. Instead, they began love the more deadly diseases, so easier to obtain regulatory approvals, and more professional treatment.
"Cash cow" increased risk of Market research firm Morningstar Inc. senior analyst DamienConover that these pharmaceutical giants hope that the excavation that the relatively low degree of market competition, the potential (for example, compared with cholesterol treatment), especially anti-cancer and anti-dementia treatment market. In the past, pharmaceutical companies have always believed that to develop anti-cancer and anti-Alzheimer drugs too costly, because the use of these drugs were relatively small. However, as the global population ages, the patients suffered against these diseases is likely increased significantly.
Large pharmaceutical companies to promote new therapeutic areas to transfer another factor is that in the past, such as heart disease as a "cash cow" of the treatment field, developed by the New Drugs Approved the listing of increasing difficulty, because the FDA against the risks of such drugs to maintain the increasing vigilance.
FDA approval of new drugs the more reason for caution is that the pharmaceutical industry in recent years have been some incidents of drug side effects. In these cases, drug side effects far more than they bring therapeutic benefits to patients. Arthritis painkiller Vioxx, for example, the study showed the drug could cause heart attack, the Merck drug company will recall from the market. Similarly, GSK to its production Diabetes Avandia medication added warning signs, because studies show that: the drug increases the risk of heart attack patients. It is these events to FDA
more than a cautious start, and for them in the present cases, there is not much need to approve an additional cholesterol-lowering drugs, because the existing drug Lipitor has been proven with for the treatment of high cholesterol a significant effect, and relatively safe.
Multiple roles in promoting R & D Fact, according to the American Enterprise Institute for Public Policy (AEI), a report published by researchers ScottGottlieb, FDA has become so cautious, so the agency within the department responsible for approving the heart drugs, over the last four years, not a one-time new drug application by a heart attack. Drugs in the FDA review team, the team responsible for heart disease drugs review the most difficult tasks facing.
However, anticancer drugs and resistance in the treatment of Alzheimer's disease drug approval on, FDA seems to be more willing to take a compromise approach, because the current market and not many drugs for the treatment of these diseases and these diseases more deadly .
Gottlieb said that when an anti-cancer drugs cause some rare but devastating side effects, people tend not to give too much attention; but if a cold medicine (or conventional painkillers) problems, quite the reverse.
Pharmaceutical companies, into these new areas of treatment there is another advantage: As the cancer and Alzheimer's fatal, they can be set to a higher price medicines. Thus, while the use of relatively few patients, but they can still be harvested from a "blockbuster" drugs.
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