Enrollment of any patient who has satisfactorily participated in Amgen BDNF 930121 Part C through 9 months without evidence of intolerable toxicity to study drug. Patients will be treated with r-metHuBDNF at the same blinded dose level assigned to them in Amgen BDNF 930121 Part C. Previous placebo patients will be randomized at a l:l ratio blocked by center to receive either 25ug/kg or 100 ug/kg r-metHuBDNF. R-metHuBDNF will be given once daily by subcutaneous injection for up to 24 months in the absence of drug-induced toxicity.

Project Start
1997-01-06
Project End
1997-11-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
37
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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