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Posts Tagged ‘pharmaceutical industry’

Stop Drug Companies from Hiding Negative Results

Posted by medconsumers on July 1, 2005

Why Do We Need A Publicly Funded, Publicly Accessible Database Of Clinical Trials?

The short answer is this: To stop the pharmaceutical and device industries from hiding the results of clinical trials that did not show a benefit to their products. And to stop them from withholding findings that indicate significant harms associated with their products.

In a perfect world, an independent group of researchers would conduct the clinical trials designed to see whether a new drug is safer or more effective than the drugs already available for the same condition. A head-to-head comparison would be conducted for at least one year. If the new drug has no advantage over the older drugs, it wouldn’t be allowed on the market.

The real world scenario, unfortunately, is far less than perfect. To receive FDA approval, a drug company need only provide two trials that proved its drug is better than nothing (a placebo). Most trials last only a few months. In 2002, Washington Post reporter, Shankar Vedantam , described a new analysis of the trials conducted by drug companies that made drugs to treat depression, such as Prozac, Paxil, and Zoloft. The majority of these trials found that placebos were just as effective as the antidepressants, and in some trials, the placebos worked better. But the public never learned about the trials that found antidepressant were ineffective. The drug companies withheld their existence and submitted the FDA-required two trials that did show a benefit to their drug. The analysis described by the Washington Post reporter also revealed that the makers of Prozac had to conduct five trials to obtain two that were positive, and the makers of Paxil and Zoloft had to conduct even more.

The issue of drug companies withholding negative trial results has slowly become more acute in the last 15 years because government funding of trials has decreased considerably. The majority of all drug trials are now conducted by the sponsoring drug companies. And it is becoming increasingly evident that the drug companies get the results they want. A 2003 review published in the BMJ (British Medical Journal) found that studies sponsored by pharmaceutical companies were far more likely to have outcomes favoring the sponsor than were studies with other sponsors . The problem is not limited to pharmaceutical research. For example, in a 2003 review of all studies that looked at total hip arthroplasty implants, 75% were commercially sponsored, of which 93% reported positive outcomes; whereas independently funded researchers reported good results in only 37% of studies.

This critical issue did not begin to penetrate the public’s consciousness until June 2004, when New York State attorney general, Eliot Spitzer, filed a lawsuit against the British-based pharmaceutical company, GlaxoSmithKline. The pharmaceutical company, one of the world’s largest, was accused of “persistent fraud” for failing to tell doctors that some of its studies of the antidepressant Paxil showed that the drug didn’t work in adolescents and might lead to suicidal thoughts. The lawsuit has since been settled.

For more than a decade, a small group of medical journal editors and researchers has periodically offered a solution that has only now gained serious attention: All clinical trials should be registered at the onset. And the registry must be publicly available. Only then will doctors and the public have complete information about all the research that has been conducted on a particular drug or device. Predictably, there is a great deal of resistance to this idea from industry. Congress is considering legislation, entitled Fair Access to Clinical Trials Act, which will mandate the early registration of clinical trials. Unfortunately, there are many problems with this proposed legislation, not the least of which is the failure to include more than drug trials in the mandate.

Some journal editors have taken a strong stand on this issue. Last year, a new policy was announced by 11 editors of the world’s most prestigious journals, including the New England Journal of Medicine, The Lancet, Canadian Medical Association Journal, and the New Zealand Medical Journal. They will not publish results of any trial that has not been registered in a publicly available database before the first participant is enrolled. The policy is aimed at foiling researchers who change the goals of a study while it is in progress and to stop drug companies from withholding the existence of trials that show negative results.

In May 2005, the 11 editors, now called the International Committee of Medical Journal Editors, updated its policy about the registration of clinical trials. The journals represented by this committee will not publish trials that are not publicly registered by July 1, 2005. The editors have given the drug companies until September 13, 2005 to register ongoing trials. Other editors from other medical journals have now joined the committee. The policy will be successful only when all medical journals take a similar stand.

The Committee defined clinical trial this way: “Any research project that prospectively assigns human subjects to intervention and comparison groups to study the cause-and-effect relationship between a medical intervention and a health outcome. By ‘medical intervention’ we mean any intervention used to modify a health outcome. This definition includes drugs, surgical procedures, devices, behavioral treatments, process-of-care changes, and the like.”

Consumers have a major stake in this issue. We cannot make informed medical decisions if we cannot trust the research. And clinical trials cannot be conducted without us. People who agree to participate in trial do so with the hope of helping themselves or future patients. To participate in a trial that never is made public means that people have risked the harm of the treatment to no benefit.

The Center for Medical Consumers recommends that people refuse to take part in any clinical trial that is not registered before recruitment. At present, the nearest thing to a publicly available registry is www.clinicaltrials.gov This Web site lists government-sponsored trials; it has been criticized for having incomplete information. Some pharmaceutical companies have begun to list their clinical trials on their respective Web sites.

Maryann Napoli, Center for Medical Consumers ©
July 2005

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Integrity in Science

Posted by medconsumers on September 1, 2003

Conference Addresses Corporate Influences on Medical Research

By Maryann Napoli
(September 2003)

The American public is concerned about the fact that many physicians and scientists have financial ties to the drug and device industries, and most people want the news media to do a better job disclosing these ties whenever experts are quoted. These results, from a survey conducted by the Center for Science in the Public Interest (CSPI), led this advocacy group to convene a recent conference in Washington, DC, entitled, “Conflicted Science: Corporate Influence on Scientific Research and Science-Based Policy.” The speakers were primarily researchers and investigative journalists who have written articles about this topic, which has become the focus of mounting concern for editors of medical journals.

Michael Jacobson, CSPI’s executive director, set the tone for the conference: “The corporate world seeks to influence science and science policy at many different levels, from the sponsorship and design of university research to the creation of scientific journals; from placing sympathetic scientists on federal and international advisory committees to generating publicity in the mass media; from influencing major health charities to creating their own friendly nonprofit organizations.” As he turned the program over to the speakers, Jacobson said that he had asked them not only to express their concerns, but also to suggest remedies.

Passive smoking is one major area followed by Lisa A. Bero, PhD, Center for Tobacco Control Research and Education, University of California, San Francisco. “Researchers funded by the tobacco industry were nine times more likely to find no relationship between ill health and passive smoking,” she found. When a 1981 study showed a link between lung disease and non-smoking women living with smokers, Dr. Bero said that the tobacco industry created its own study to refute it. For example, the industry funded studies found ill effects of other sources of indoor air pollution to distract from the importance of secondhand smoke, reported Dr. Bero. Another common tactic was to create doubt in the media about the studies that showed adverse health effects associated with smoking and to characterize such findings as “controversial.”

Drummond Rennie, MD, deputy editor of the Journal of the American Medical Association, pointed out that drug companies often set up comparison trials designed in such a way that their products are bound to come out on top. He gave as example the clinical trial Pfizer designed for its oral drug fluconazole (Diflucan), which treats yeast infections and toenail fungus. To prove that fluconazole is best at treating the potentially fatal funguses that afflict people with AIDS, Pfizer tested its drug against oral versions of competitors’ antifungal drugs-one of which should have been given only intravenously and the other already known to be ineffective in people with AIDS.

Secretiveness is also a major problem. To the drug industry, “everything is a trade secret, even the very existence of a clinical trial,” Dr. Rennie said, referring to the fact that industry-sponsored trials that produce negative results often go unpublished. The remedy for this problem, he said, would be the required registration of all trials at inception. That way a drug company cannot hide the number of trials that come up with results unfavorable to their products. As for the common problem of university researchers with financial ties to industry, Dr. Rennie noted, wryly, “What is called conflict of interest is called synergy by Wall Street.”

Dr. Rennie alluded to two high-profile cases in which researchers found that the cheaper, older drug was not only more effective, but also safer than newer products. In both cases, the drug companies whose products were in danger of losing market share attacked the researchers’ credibility and initiated lawsuits to stop them from going public with the results.

Two weight loss drugs sold in the combination called “fen-phen” made news in the 1990s because they caused heart valve damage. Investigative reporter Alicia Mundy, who wrote a book on the topic, told the conference how much she learned about the use of medical studies as public relation tools while searching the files of Wyeth-Ayerst Laboratories. Her book Dispensing With the Truth “documents how this drug company and its partners knew about the diet drugs’ links to an increasing number of deaths from a lung disease and to major heart valve damage, and did not reveal this to doctors, to the press, or to the FDA.” About 7 million people took the drugs from 1994 to 1997.

After the diet drugs Redux and Pondimin (the “fen” of the “fen-phen” combination) were withdrawn in 1997 at the urging of the FDA, the manufacturers put their considerable resources toward damage control. A 1998 front-page story in USA Today proclaimed, “Study: No heart damage from diet drug.” The source of the headline was a study presented by Dr. Neil Weissman at an American College of Cardiology conference, and the upbeat news was also reported in The New York Times. Mundy said that her investigative work led her to this scoop: After the conference, Dr. Weissman sent his study to The New England Journal of Medicine, which provisionally rejected it. Mundy found that the Journal editor had sent a letter to Dr. Weissman, telling him to recalculate his results using a methodology suggested by the Journal’s reviewers.

Once Dr. Weissman complied, Mundy said, his results were quite different. A significant link was shown between heart-valve damage and the drug Redux. Two other studies eventually found the same link, but when the recalculated study was eventually published by The New England Journal, the revised findings never got the same media attention. “No one noticed,” observed Mundy, that the lead researcher was the same Weissman who, only six months earlier, had dismissed the heart-valve problems.

“We don’t hear much about the fen-phen story anymore,” noted Mundy, explaining the reason. The people who brought lawsuits against Wyeth-Ayerst because they had been harmed by these diet drugs had to sign confidentiality agreements that prevent them from warning others.

One common way drug companies can easily get free air time for their sales pitches is the video news release (VNR), which is an ad disguised as objective reporting. TV stations love these VNRs because they save them money and feed the desire for news with a positive spin, according to Trudy Lieberman, a journalist and director of the Center for Consumer Health Choices at Consumers Union. She tracked the Cytyc Corporation’s VNRs for its new Pap test technology called ThinPrep. “It followed the standard VNR formula,” explained Lieberman, “It is patient-based, always positive and always provides a take-away message: have this test, buy this product, ask your doctor.”

Lieberman encountered the same “patient” in dozens of stories in print and TV. Her name is Peggy Smith, and she tells women that ThinPrep had saved her life. What harm do these disguised ads cause, asked Lieberman, rhetorically. “There is no evidence that this technology saves lives, though ThinPrep does generate a lot of false-positive results and unnecessary investigations,” she said, “And the people viewing these VNRs probably do not have a clue that they are ads.”

Of the remedies suggested by the speakers, full disclosure was on everyone’s list. One can’t help but notice, however, that the media are currently doing an uneven job in this regard. For example, last November, The New England Journal of Medicine published a major study that found testing people for C-reactive protein might be more useful in determining heart disease risk than cholesterol screening. The media were filled with upbeat quotes about the importance of C-reactive protein testing from the lead author, Paul M. Ridker, MD. However, virtually all the news stories left out the information that Dr. Ridker holds a patent on the new test, a fact disclosed in small print at the end of his study in The New England Journal of Medicine.

On the other hand, some journalists are doing their jobs. When the National Cholesterol Education Program revised their guidelines in 2001 by lowering the level at which people were considered to have dangerously high cholesterol, Thomas Burton and Chris Adams of The Wall Street Journal noted that 36 million people now had high cholesterol which automatically triples the number of Americans who are candidates for cholesterol-lowering drugs. Burton and Adams also noted that five of the 14 members of the committee that made this decision were either consultants to, or had received honorariums from, companies that made cholesterol-lowering drugs.

Though people often view non-profit health organizations as objective, many take industry funding that could compromise their advice to the public. To let consumers and journalists know who takes money from whom, the conference sponsor, Center for Science in the Public Interest, or CSPI, has compiled a long list of non-profit professional organizations and charities with ties to industry. For example, the American Heart Association accepted $400,000 from Merck, makers of a top-selling cholesterol-lowering drug, to teach 40,000 doctors to treat cholesterol according to guidelines.

For a copy of “Lifting the Veil of Secrecy: Corporate Support for Health and Environmental Professional Associations, Charities, and Industry Front Groups,” send a $15 check to CSPI, 1875 Connecticut Ave., Ste 300, Washington, DC 20009-5728. Attn: Adam Pearson.

For a copy of “Lifting the Veil of Secrecy: Corporate Support for Health and Environmental Professional Associations, Charities, and Industry Front Groups,” send a $15 check to CSPI, 1875 Connecticut Ave., Ste 300, Washington, DC 20009-5728. Attn: Adam Pearson.

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Links: Government Agencies

Posted by medconsumers on January 1, 2000

Centers for Disease Control and Prevention
This government agency’s Web site contains the latest in health news as well as an extensive listing of fact sheets on a variety of diseases and health related issues.

FDA Homepage
Find out about drug recalls, recent drug approvals, and other pharmaceutical information at the Food and Drug Administration’s Web site.

Occupational Safety and Health Administration
Learn more about how to prevent injuries caused by the workplace and the regulations set to ensure on-the-job safety.

National Institute of Health
Information about government-funded medical research.

New York State Department of Health
The New York State Department of Health is responsible for all public health activities throughout the state as well as oversight of licensed health care facilities such as hospitals, nursing homes and ambulatory surgery centers and physician and physician assistants.

U.S. Department of Health & Human Services
The U.S. Department of Health and Human Services is responsible for the work of 11 agencies, including the Center for Medicare and Medicaid Services (CMS), the National Institutes of Health (NIH) and the Food and Drug Administration (FDA) among others.

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Links: Drugs

Posted by medconsumers on January 21, 1982

American Medical Students Association
AMSA grades medical schools on the presence or absence of a policy regulating the interactions between their students and faculty and the pharmaceutical and device industries. Working with The Prescription Project, the AMSA developed a rigorous and transparent methodology to assess the content of policies at medical schools throughout the country.

www.besttreatments.org/risk
British Medical Journal Publishing Groupand United HealthCare Services provide help in understanding risks and benefits when deciding to take a drug.

Consumer Reports
Free in-depth reports about safety and effectiveness of 12 commonly prescribed drugs. Emphasis is on price.

DrugAlerts.com
Latest on drug recalls, FDA warnings, and drugs in litigation. Site is sponsored by trial lawyers.

Drugs.com
DrugWatch.com
Both Web sites provide free information about drugs, including indications, side effects, and warnings.

FDA Homepage
Find out about drug recalls, recent drug approvals, and other pharmaceutical information at the Food and Drug Administration’s Web site.

MedWatch
MedWatch, the FDA medical products reporting program, allows consumers to report and read about serious reactions and problems with drugs and medical devices.

National Institute for Health Care Management Research and Educational Foundation
Learn more about the relationship between higher drug costs and the federal laws which protect the pharmaceutical industry from competition in the making and marketing of drugs. See how much the Pharmaceutical industry spends advertising the most expensive prescription rugs directly to consumers.

No Free Lunch
Physicians, medical students and residents concerned about the influence of the pharmaceutical industry – especially freebies.

Number Needed to Treat
How many people have to be treated with a drug to save one life or prevent one serious occurrence (e.g.,stroke or heart attack)?

The People’s Pharmacy
Web site of pharmacist Joe Graedon and his wife Terry, who have long written a syndicated newspaper column. Mostly about drugs but home remedies are also discussed because visitors are encouraged to ask questions.

PHARMALOT
A blog that provides commentary on the pharmaceutical industry and related litigation.

Public Citizen Health Research Group
This Ralph Nader-affiliated consumer advocacy organization serves primarily as an FDA Watchdog, petitioning the agency to get dangerous drugs and devices off the market.  Free access to several sample issues of its Health Letter.

Therapeutics Initiative
Based at University of British Columbia, Vancouver, Therapeutics Initiative publishes a free online newsletter about drugs that is aimed primarily at physicians. Check out the podcasts.

www.medicationsense.com
Dr. Jay S. Cohen provides articles about prescription drugs and how often people stop taking them because the dose is too high.

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