30
Participants
Start Date
November 30, 2000
Primary Completion Date
May 31, 2003
Study Completion Date
March 31, 2009
QS21
"* Treatment schedule and dose: Thirty patients will be treated with specified doses of each carbohydrate or peptide constituent as has been determined. QS21 will be administered at the standard dose of 100 ug.~* Sites: The vaccine conjugate will be administered subcutaneously on a rotating basis to random sites on the upper arms and upper legs.~* Dose modifications: If a patient experiences a Grade III or greater local or Grade II or greater systemic toxicity at any time a decrease by 50% in all components of future vaccinations will be administered for that patient. Any evidence of autoimmunity, however, will result in a cessation of immunization in that patient."
Memorial Sloan-Kettering Cancer Center, New York
Collaborators (1)
Capcure
UNKNOWN
Memorial Sloan Kettering Cancer Center
OTHER