Sent: Friday, February 23, 2001 11:58 AM
Subject: [Direito_Saude] NOSSAS CRIANCAS VAO SER COBAIAS NOS EUA ? ( A Amazonia nao eh suficiente ... )

 
 
Vejam  esta mat�ria do Washington Post de hoje, 23/2.    Agora querem testar uma droga de uma empresa de  biotecnologia em crian�as carentes da Am�rica Latina  que  t�m problemas respirat�rios.   A droga n�o tem licen�a  para uso nos Estados Unidos.   A empresa est� pedindo �  Food and Drug  Administration essa permiss�o.
 
 
 
Segue o texto na �ntegra:

 

The Food and Drug Administration is weighing whether to  approve a Pennsylvania biotechnology company's proposal  to conduct an experiment that would leave hundreds of  sick,   premature infants in Latin America  without  proven  lifesaving medications.
 

 
The experiment would be considered unethical in the  United States, where researchers are not allowed to use  placebos -- or dummy medicines -- on test subjects  suffering from potentially fatal illnesses for which  there are proven treatments. But Robert J. Capetola,
president of Discovery Laboratories of Doylestown, Pa.,  said its planned tests on newborns with a serious lung  disease could shave 18 months off of the development of
an important drug.
 
 

In some poor Latin American hospitals, Capetola said,  infants with the lung illness may not have access to  established drugs and would not be left worse off by  placebo treatment.   He said infants in the study would  receive better care than is currently available because  Discovery would donate ventilators and antibiotics for  their use.

 
 
 
The company wants the FDA to approve the research in  case it wants to use the test results to try to market  the drug Surfaxin in the United States for treatment of  respiratory distress syndrome. The study would divide  infants into three groups: those on Discovery's  experimental lung medication, those who get another  established drug, and a third group that would get only  placebo treatment.

 
 
That design would enable the company to show whether its  unproven product is better than a competitor's but also  whether it's better than no treatment at all.

 
 
Disclosure of the proposed Latin American experiments  comes at a time of mounting concern that drugmakers in  the United States and other wealthy nations are  increasingly testing new medicines in developing  countries where costs are low, patients plentiful and  government oversight lax.    Placebo trials in particular  have generated heated international debate since the mid -1990s,  prompted in large part by HIV tests in Thailand  and Africa that withheld proven drugs from some pregnant  women whose children then were born infected with the  virus that causes AIDS.
 

 
It would be virtually impossible for a company to  include a no-treatment group in a test on the infant  lung illness in the United States because standard care  in American hospitals -- and in most developed  countries -- calls for using established drugs known as
surfactants that significantly reduce newborn deaths and  complications.
 
 
 

Withholding lifesaving care for respiratory distress  syndrome for the sake of a drug experiment  is "considered unethical in the USA," according to an  FDA document discussing the Discovery Laboratories  proposal.

 
 

Discovery also plans an experiment on newborns in  Europe, Capetola said, where all infants tested would  receive some drugs:   either Discovery's experimental
surfactant or another already approved surfactant.
 


In the Latin America study, Capetola said that using a  placebo group would produce faster comparative  results. "We think it would be totally unethical not to  conclude it and get it to patients quicker," he said.

 
 
But Sidney M. Wolfe, director of the watchdog  organization Public Citizen's Health Research Group,  yesterday called the test "totally unethical." His group  released FDA documents about the proposal and called on  both the FDA and U.S. Department of Health and Human  Services to halt the research.

 
 
 
"It is the worst kind of race to the ethical bottom,"  said Peter Lurie, deputy director of Public Citizen's  Health Research Group. Surfactant treatment for a  premature infant in the United States costs between  $1,100 and $2,400.   He said Latin American families would
be taking part in a test of a product that would  ultimately be too expensive for them to afford.
 


But Capetola said that if Surfaxin proves successful it  will be sold at a reduced price to the Latin American  countries that hosted the research.
 
 

Respiratory distress syndrome is the fourth-largest  cause of infant mortality in the United States.    In 1990,  the FDA approved the first commercially available  surfactant, a drug that reduces tension in the infants'  tiny lung air sacs.  Four surfactants are now marketed in the United States.
 


HHS spokesman Bill Hall said Secretary Tommy G.  Thompson "would not get involved in a regulatory  issue . . .  That's for the FDA to decide."
 
 
 

Janet Woodcock, director of the FDA's Center for Drug  Evaluation and Research, said Discovery's proposed  experiment remains  "under consideration."   If the agency
concludes the design is unethical,  she said, the drug's  developers could legally perform the trial outside the  United States.   But the FDA might refuse to accept the  findings as proof the drug is safe enough for Americans,  she added.

 
The Surfaxin proposal was discussed at an FDA ethics  round table a month ago specifically because there is a  division of opinion inside the agency on the ethical
questions it raises, Woodcock said.
 
 
 

The growth in overseas testing was documented in  December in a Washington Post series called "The Body  Hunters." The articles recounted instances in which  American researchers had conducted experiments in  impoverished nations that would have been forbidden in  the United States.



� 2001 The Washington Post Company


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