Subir Roy: Clinical trials gone haywire

There is no independent audit to investigate the cause of death and the regulator simply takes the word of the investigator

A decade ago India was the new kid on the block in clinical trials, a part of the contract research space. The Indian advantage lay in low cost skills and patient diversity — the poor as well as the rich, with lifestyle diseases. Ashish Dasgupta, an industry veteran then with Lambda Therapeutic, a contract research organisation (CRO), had said, “Indian CROs can be very competitive but must not be complacent. The global market has a lot of expectation from India.” (Made in India, 2005, by this writer.)

Some of that expectation has been belied. The clinical trial industry has been through hell in the last few months, prompting Mr Dasgupta, now vice-chairman of the Association of Contract Research Organisations (ACRO) in India, to say, “irregularities should teach stakeholders how to tighten regulations and bring about better compliance... People have instead tarnished the industry’s image.”

The subject has become emotive and controversial, taking on the attributes of a scandal, with a sharp rise in the number of deaths among subjects participating in revealed by the government in Parliament, moving the courts on the matter through public interest litigation and Supreme Court judges issuing obiter dicta reflective of the public mood built up ahead of pronouncement of actual judicial verdict.

Last August Health Minister told Parliament that 1,725 deaths had taken place in India among subjects participating in over a four-year period (2007-10), with the figure going up sharply from 132 in 2007 to 668 in 2010. However, there was a fall in deaths in 2011 to 438 which has been attributed to a slowdown in new trials launched to 169 in 2011 from 254 in 2010, as reported by the Financial Express.

In March this year the Supreme Court took on board a public interest litigation filed by a group of doctors alleging that illegal and unethical were being conducted in Indore by multinationals on vulnerable members of society, resulting in deaths, and asked the government and the Medical Council of India to file their responses in six weeks. Earlier this month, when the matter came up again before the court its mood had hardened as the Centre and the Madhya Pradesh government had not come up with their responses. The court said, “There has to be some sense of responsibility. Human beings are being treated as guinea pigs. This is unfortunate.”

As it happens, a large number of deaths have taken place among subjects of conducted on behalf of several MNCs and leading Indian firms like Novartis, Quintiles, Pfizer, Sun Pharma and Jubilant, as reported by Business Standard. Quintiles, a global leader in contract research, has emphasised that those participating in are already afflicted and so death during trials need not be caused by the trials. That is indisputable — but there is dark irony in Quintiles having to defend itself when it pioneered in India in 1997 and had then rooted for India by asserting, “Doing work here is globally competitive, emphatically so,” again in Made in India.

But there is another side to the deaths. The Tribune quotes Chandra Gulhati, who it says has led several in the UK and is now investigating deaths which have occurred in Indore, as saying that the number of deaths will be much more than we will ever know. There is to and the regulator simply takes the word of the investigator if it says that a death took place owing to prior illness. Such investigators are hired by the firm seeking to test its new entity, so “how can we expect them to be objective all the time?”

There is also the issue of how or where a trial is conducted. Apurva Shah, chairman of in India, has asserted that studies conducted in Indore, now the subject of court scrutiny, do not involve any major CRO. This may be so, but Indian CROs have a history to live down. In 2004 there was a scandal of sorts when the World Health Organisation withdrew its approval of cheap anti-retroviral drugs — used in the global fight against AIDS — manufactured by some leading Indian drug companies because the bio-equivalence studies for them conducted by CROs in India were faulty. This column had then observed, “It is tragic that the bad influence of poor domestic standards has blotted the Indian drug industry’s copybook and severely set back the industry. The redeeming feature is that there will now be a shakeout in the industry.” In a subsequent column, we will examine the ethics of our doctors and the state of regulation.


subirkroy@gmail.com  

image
Business Standard
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Business Standard

Subir Roy: Clinical trials gone haywire

There is no independent audit to investigate the cause of death and the regulator simply takes the word of the investigator

Subir Roy 

A decade ago India was the new kid on the block in clinical trials, a part of the contract research space. The Indian advantage lay in low cost skills and patient diversity — the poor as well as the rich, with lifestyle diseases. Ashish Dasgupta, an industry veteran then with Lambda Therapeutic, a contract research organisation (CRO), had said, “Indian CROs can be very competitive but must not be complacent. The global market has a lot of expectation from India.” (Made in India, 2005, by this writer.)

Some of that expectation has been belied. The clinical trial industry has been through hell in the last few months, prompting Mr Dasgupta, now vice-chairman of the Association of Contract Research Organisations (ACRO) in India, to say, “irregularities should teach stakeholders how to tighten regulations and bring about better compliance... People have instead tarnished the industry’s image.”

The subject has become emotive and controversial, taking on the attributes of a scandal, with a sharp rise in the number of deaths among subjects participating in revealed by the government in Parliament, moving the courts on the matter through public interest litigation and Supreme Court judges issuing obiter dicta reflective of the public mood built up ahead of pronouncement of actual judicial verdict.

Last August Health Minister told Parliament that 1,725 deaths had taken place in India among subjects participating in over a four-year period (2007-10), with the figure going up sharply from 132 in 2007 to 668 in 2010. However, there was a fall in deaths in 2011 to 438 which has been attributed to a slowdown in new trials launched to 169 in 2011 from 254 in 2010, as reported by the Financial Express.

In March this year the Supreme Court took on board a public interest litigation filed by a group of doctors alleging that illegal and unethical were being conducted in Indore by multinationals on vulnerable members of society, resulting in deaths, and asked the government and the Medical Council of India to file their responses in six weeks. Earlier this month, when the matter came up again before the court its mood had hardened as the Centre and the Madhya Pradesh government had not come up with their responses. The court said, “There has to be some sense of responsibility. Human beings are being treated as guinea pigs. This is unfortunate.”

As it happens, a large number of deaths have taken place among subjects of conducted on behalf of several MNCs and leading Indian firms like Novartis, Quintiles, Pfizer, Sun Pharma and Jubilant, as reported by Business Standard. Quintiles, a global leader in contract research, has emphasised that those participating in are already afflicted and so death during trials need not be caused by the trials. That is indisputable — but there is dark irony in Quintiles having to defend itself when it pioneered in India in 1997 and had then rooted for India by asserting, “Doing work here is globally competitive, emphatically so,” again in Made in India.

But there is another side to the deaths. The Tribune quotes Chandra Gulhati, who it says has led several in the UK and is now investigating deaths which have occurred in Indore, as saying that the number of deaths will be much more than we will ever know. There is to and the regulator simply takes the word of the investigator if it says that a death took place owing to prior illness. Such investigators are hired by the firm seeking to test its new entity, so “how can we expect them to be objective all the time?”

There is also the issue of how or where a trial is conducted. Apurva Shah, chairman of in India, has asserted that studies conducted in Indore, now the subject of court scrutiny, do not involve any major CRO. This may be so, but Indian CROs have a history to live down. In 2004 there was a scandal of sorts when the World Health Organisation withdrew its approval of cheap anti-retroviral drugs — used in the global fight against AIDS — manufactured by some leading Indian drug companies because the bio-equivalence studies for them conducted by CROs in India were faulty. This column had then observed, “It is tragic that the bad influence of poor domestic standards has blotted the Indian drug industry’s copybook and severely set back the industry. The redeeming feature is that there will now be a shakeout in the industry.” In a subsequent column, we will examine the ethics of our doctors and the state of regulation.


subirkroy@gmail.com  

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Subir Roy: Clinical trials gone haywire

There is no independent audit to investigate the cause of death and the regulator simply takes the word of the investigator

A decade ago India was the new kid on the block in clinical trials, a part of the contract research space. The Indian advantage lay in low cost skills and patient diversity — the poor as well as the rich, with lifestyle diseases. Ashish Dasgupta, an industry veteran then with Lambda Therapeutic, a contract research organisation (CRO), had said, “Indian CROs can be very competitive but must not be complacent. The global market has a lot of expectation from India.” (Made in India, 2005, by this writer.

A decade ago India was the new kid on the block in clinical trials, a part of the contract research space. The Indian advantage lay in low cost skills and patient diversity — the poor as well as the rich, with lifestyle diseases. Ashish Dasgupta, an industry veteran then with Lambda Therapeutic, a contract research organisation (CRO), had said, “Indian CROs can be very competitive but must not be complacent. The global market has a lot of expectation from India.” (Made in India, 2005, by this writer.)

Some of that expectation has been belied. The clinical trial industry has been through hell in the last few months, prompting Mr Dasgupta, now vice-chairman of the Association of Contract Research Organisations (ACRO) in India, to say, “irregularities should teach stakeholders how to tighten regulations and bring about better compliance... People have instead tarnished the industry’s image.”

The subject has become emotive and controversial, taking on the attributes of a scandal, with a sharp rise in the number of deaths among subjects participating in revealed by the government in Parliament, moving the courts on the matter through public interest litigation and Supreme Court judges issuing obiter dicta reflective of the public mood built up ahead of pronouncement of actual judicial verdict.

Last August Health Minister told Parliament that 1,725 deaths had taken place in India among subjects participating in over a four-year period (2007-10), with the figure going up sharply from 132 in 2007 to 668 in 2010. However, there was a fall in deaths in 2011 to 438 which has been attributed to a slowdown in new trials launched to 169 in 2011 from 254 in 2010, as reported by the Financial Express.

In March this year the Supreme Court took on board a public interest litigation filed by a group of doctors alleging that illegal and unethical were being conducted in Indore by multinationals on vulnerable members of society, resulting in deaths, and asked the government and the Medical Council of India to file their responses in six weeks. Earlier this month, when the matter came up again before the court its mood had hardened as the Centre and the Madhya Pradesh government had not come up with their responses. The court said, “There has to be some sense of responsibility. Human beings are being treated as guinea pigs. This is unfortunate.”

As it happens, a large number of deaths have taken place among subjects of conducted on behalf of several MNCs and leading Indian firms like Novartis, Quintiles, Pfizer, Sun Pharma and Jubilant, as reported by Business Standard. Quintiles, a global leader in contract research, has emphasised that those participating in are already afflicted and so death during trials need not be caused by the trials. That is indisputable — but there is dark irony in Quintiles having to defend itself when it pioneered in India in 1997 and had then rooted for India by asserting, “Doing work here is globally competitive, emphatically so,” again in Made in India.

But there is another side to the deaths. The Tribune quotes Chandra Gulhati, who it says has led several in the UK and is now investigating deaths which have occurred in Indore, as saying that the number of deaths will be much more than we will ever know. There is to and the regulator simply takes the word of the investigator if it says that a death took place owing to prior illness. Such investigators are hired by the firm seeking to test its new entity, so “how can we expect them to be objective all the time?”

There is also the issue of how or where a trial is conducted. Apurva Shah, chairman of in India, has asserted that studies conducted in Indore, now the subject of court scrutiny, do not involve any major CRO. This may be so, but Indian CROs have a history to live down. In 2004 there was a scandal of sorts when the World Health Organisation withdrew its approval of cheap anti-retroviral drugs — used in the global fight against AIDS — manufactured by some leading Indian drug companies because the bio-equivalence studies for them conducted by CROs in India were faulty. This column had then observed, “It is tragic that the bad influence of poor domestic standards has blotted the Indian drug industry’s copybook and severely set back the industry. The redeeming feature is that there will now be a shakeout in the industry.” In a subsequent column, we will examine the ethics of our doctors and the state of regulation.


subirkroy@gmail.com  

image
Business Standard
177 22

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