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Biotech / Medical : IDPH--Positive preliminary results for pivotal trial of ID
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To: Roudy who wrote (1416)1/13/1998 1:54:00 AM
From: Maurice Winn  Read Replies (1) of 1762
 
Don, just a little bit of info, but a doctor here in the haematology department of Auckland Hospital claims not to think much of Rituxan, preferring I131 treatment prospects.

New Zealand will be a while yet approving Rituxan. Maybe 6 months. It remains a puzzle to me as to why the FDA only approves it for follicular low grade lymphomas when anything with a CD20 hanging around should be approved. With the minimal side effects compared with the shambles that cyclophosphamide, vincristine and adriamycin cause in a person it seems crazy not to use it anywhere CD20 cells are being targeted as an adjunct therapy. Safety was established in other trials. Efficacy seems obvious.

What is being achieved by making a rigmarole of approvals for other CD20 antigen lymphomas?

It beats me why New Zealand should add six months to approvals. Smells like bureaucracy. Maybe marketing slackness by the companies who are supposed to promote it here.

Bloody hopeless in my opinion.

Meanwhile, people who could be helped will suffer and die, the beneficiaries of their wills will blow the money on gin instead of treatment, the companies who produce and sell the product forego income.

Maurice
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