Top Indian hospital to probe baby deaths in clinical trials



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NEW DELHI, August 20, 2008 (AFP) - India's top medical facility will investigate the deaths of 49 babies in clinical trials that took place from the beginning of 2006 to the present, a hospital official said Wednesday.

'An internal inquiry has been ordered,' Shakti Kumar Gupta, head of administration for the state-run All-India Institute of Medical Sciences (AIIMS), told AFP.

'We have constituted a committee to inquire into this.'

The country's biggest hospital, where thousands go for free top medical treatment, has been in the spotlight after a non-profit health group publicised infant deaths that occurred during clinical trials over the last 30 months, some of them associated with foreign drug companies.

Some 4,142 babies admitted in the hospital were in clinical trials since January 1, 2006, more than half of them under the age of one, the hospital told the group in response to a request under freedom-of-information laws.

The non-profit's founder said it hoped to publicise the need for better regulation of India's booming outsourced clinical trial business, estimated at about 120 million dollars last year and growing at 25 percent annually.

'When you are not able to afford a particular treatment in a private health care centre you look forward to getting free medication in something like this,' said Rahul Verma, of the Uday Foundation for Congenital Defects and Rare Blood Groups, which filed the request.

'We wanted to know what are the socioeconomic condition of these people? Are they given consent forms and counselling?'

Verma said the hospital did not provide information on the incomes of the families in the infant trials.

India has become a popular destination for clinical research because of its huge population, varied population and low costs. Trials here cost 40 to 60 percent of what they would in developed countries.

Consulting firm Ernst & Young has said the outsourced clinical research market in India could grow to two billion dollars by 2010.

But with many of those who participate in trials poor and often literate, with few other options for care, questions persist over the ethics of doing the human testing of new drugs here.



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