A Phase I, Multicenter, Dose Escalation Study of CAT-8015 in Participants With Chronic Leukemia

PHASE1TerminatedINTERVENTIONAL
Enrollment

11

Participants

Timeline

Start Date

March 7, 2007

Primary Completion Date

April 7, 2008

Study Completion Date

April 7, 2008

Conditions
Leukemia, Lymphoma, Chronic LymphocyticLeukemia, Prolymphocytic Leukemia, SmallLymphocytic Lymphoma, Moxetumomab Pasudotox
Interventions
DRUG

CAT-8015 5 mcg/kg

Participants received a single intravenous infusion of 5 mcg/kg moxetumomab pasudotox (CAT-8015) on Days 1, 3, and 5 of every 28-day cycle and continued cycles of therapy until progressive disease (PD) or until otherwise they become ineligible.

DRUG

CAT-8015 10 mcg/kg

Participants received a single intravenous infusion of 10 mcg/kg moxetumomab pasudotox (CAT-8015) on Days 1, 3, and 5 of every 28-day cycle and continued cycles of therapy until progressive disease (PD) or until otherwise they become ineligible.

DRUG

CAT-8015 20 mcg/kg

Participants received a single intravenous infusion of 20 mcg/kg moxetumomab pasudotox (CAT-8015) on Days 1, 3, and 5 of every 28-day cycle and continued cycles of therapy until progressive disease (PD) or until otherwise they become ineligible.

Trial Locations (3)

Unknown

Research Site, Indianapolis

Research Site, Bethesda

Research Site, Lodz

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Cambridge Antibody Technology

OTHER

lead

MedImmune LLC

INDUSTRY