Multivalent Conjugate Vaccine Trial for Patients With Biochem. Relapsed Prostate Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

November 30, 2000

Primary Completion Date

May 31, 2003

Study Completion Date

March 31, 2009

Conditions
ProstateCancer
Interventions
BIOLOGICAL

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."

Trial Locations (1)

10065

Memorial Sloan-Kettering Cancer Center, New York

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Capcure

UNKNOWN

lead

Memorial Sloan Kettering Cancer Center

OTHER

NCT00579423 - Multivalent Conjugate Vaccine Trial for Patients With Biochem. Relapsed Prostate Cancer | Biotech Hunter | Biotech Hunter