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The late “flameout” of the boob cancer dose Avastin “leave beat a decisive examination” on whether FDA volition “birth the bravery to turnabout row when a aesculapian handling that it sanctioned based on overture grounds flops poorly in review studies,” the New York Times says in an column.
The Times argues that FDA “has seldom remote drugs that were presumption accelerated commendation and sometimes has failed evening to oblige culmination of reexamination studies.” However, “thither are signs it may get tougher,” the column continues, terminal, “With Avastin, the reexamination studies were accomplished in a well-timed style — with such meagre results that secession seems the compensate reply” ( New York Times , 7/26).
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Nothing brave almost that posted by Eli on 27 Jul 2010 at 2:41 am
To penalize a party for complemental it’s allegiance in a well-timed way and not dragging the followup studies for ten years alike others let through, is unjust.
To absent a dose, that shows approximately efficaciousness and does not do practically damage, from the marketplace, is unwarranted.
There’s naught brave almost that.
The FDA should forget the flow reading as it is.
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