Poor Merck. Their contention that its Vioxx painkiller raised the risk of heart attack or stroke only after 18 months' usage was contradicted Monday by the New England Journal of Medicine.
Correcting the results of the Merck-sponsored APPROVe study it previously published, the Journal suggested the increased health risk started earlier for Vioxx patients, but didn't specify a time frame.
The correction escalated the debate about Vioxx, the drug Merck pulled off the market in September 2004 after the study found the elevated health danger. The company faces more than 11,500 lawsuits over the drug, and has won half of the six cases in the court trials completed so far.
The Journal reported that the original article about the study used a faulty statistical analysis, which Merck itself disclosed earlier this year. But while company experts contended the mistake didn't affect conclusions about when the danger risk begins, the Journal disagreed.
"Therefore, statements regarding an increase in risk after 18 months should be removed," from the article that reported the study results, the Journal said.
Lawyers suing Merck on behalf of Vioxx patients or their survivors argued that the Journal correction significantly undercut Merck's legal contentions.
"I think that judges are almost required now to grant new trials in the cases where Merck has won, because the linchpin of Merck's defense has always been the 18-month argument," said "Hotshot" Mark Lanier, a Texas attorney who won a $253 million Vioxx verdict against the firm last year. "It turns out that 18 months is bogus, and it's bogus because of Merck's own internal mistakes."
Christopher Seeger, a New York attorney who last year lost a Vioxx case in which shorter-term usage of the drug was an issue, said he plans to add the Journal correction to his legal arguments seeking a new trial.
"This removes a major hurdle to getting verdicts against Merck," Seeger said.
Source: USA Today
Thanks to jimbo for this link.
3 comments:
There were seven academic "investigators"
(including first author) on the APPROVE paper.
We hear that Merck cheated the results.
Where were those authors?
Did they see the raw data?
Did they perform statistical analyses themselves?
If not why not?
If statistically incompetent did any authors think
to send data to a third party statistician for
checking?
If not, why not?
If they did, how is it possible that this
could have escaped undetected?
Is this research misconduct?
Merck used these investigators to give
research a veneer of University respectability.
All seemingly accepted what the company said with
blind faith (as do the regulators).
How long before Seeger and Lanier name one of
these paid "academic" authors or a University as chief respondent in a case? This might usefully sharpen some minds out there.
Aubrey Blumsohn
Conflicts of interest:
http://www.slate.com/id/2133061/
The links to the pdfs of NEJM stories are currently free here.
http://content.nejm.org/cgi/reprint/NEJMx060029v1.pdf
and
http://content.nejm.org/cgi/reprint/NEJMp068137v1.pdf
Thanks jimbo.
Have added the links to the piece.
Jack aka Insider
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