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Biotech / Medical
Biogen
An SI Board Since August 1996
Posts SubjectMarks Bans Symbol
1686 75 0 BIIB
Emcee:  Harold Engstrom Type:  Unmoderated
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1461I was afraid that channel stuffing was the real issue and sold most of my holdinCacaito-7/19/2002
1460Cacaito, it is now clear that BGEN stuffed the Avonex channel last year by gettiaknahow-7/19/2002
1459I suppose that if you get another request for a complete response after having saknahow-7/18/2002
1458Thanks, Georgetom pope-7/18/2002
1457The worst seems to be the Class II, then Biogen is curing itself in health proviCacaito-7/18/2002
1456There are two types of Complete Response letters. The FDA does not disclose whaaknahow-7/18/2002
1455and the difference is?tom pope-7/18/2002
1454Approval date for Amevive contingent on whether BGEN received a Class I or Clasaknahow-7/18/2002
1453duplicatdRRRoarr-7/7/2002
1452erasdRRRoarr-7/7/2002
1451erRRRoarr-7/7/2002
1450erasedRRRoarr-7/7/2002
1449Does anyone know when the results are due from the first phase III trial of Antescaram(o)uche-7/1/2002
1448Great job with the webcast annual meeting. an example that should be followed baknahow-6/14/2002
1447Are you implying that this companies management did not lie about what the FDA saknahow-6/14/2002
1446<i>This is a quote from BGEN's press release. "FDA is requesting JEB-6/14/2002
1445This is a quote from BGEN's press release. "FDA is requesting clarificaknahow-6/14/2002
1444They asked DNA for more data. They are asking BGEN for clarification of existinJEB-6/14/2002
1443Ask yourself does the FDA require every company to provide a complete response aaknahow-6/13/2002
1442I sell the government. I have to clarify simple typographical matters all the tJEB-6/13/2002
1441JEB, in spite of what Cacaito says, I never expected the FDA to ask for "neaknahow-6/13/2002
1440LOL, ...;-)JEB-6/13/2002
1439Jeb, He knows that very well, he hoped a "new pre approval" trial, it Cacaito-6/13/2002
1438A post - market trial is called a Phase IV trial. It is a trial performed as a JEB-6/13/2002
1437I am not insisting on August. Correct me if I am wrong but after the FDA commitaknahow-6/13/2002
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