SAR3419 Administered Weekly in Patients With Relapsed/Refractory CD19-positive B-cell Non-Hodgkin's Lymphoma

• Status: Completed
• Trial end date: 2012-06-01
• Target enrollment: 0
• Participant gender: All

Summary

The primary objective is to determine the maximum tolerated dose (MTD) of SAR3419 according to the dose limiting toxicities (DLTs) observed when administered as a single agent once weekly.

Secondary objectives are:

• to characterize the global safety profile

• to evaluate the pharmacokinetic (PK) profile of SAR3419 in the proposed dosing schedule

• to assess preliminary evidence of anti-lymphoma activity.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Sanofi

Criteria

Inclusion Criteria:

• Diagnosis of B-cell non Hodgkin's lymphoma

• Relapsed or refractory after standard treatments and with no curative option with conventional therapy (Patients having undergone stem cell transplantation may be included)

• CD19 positive disease by flow cytometry or immunohistochemistry

Exclusion Criteria:

• Burkitt's lymphoma, Lymphoblastic lymphoma, Chronic lymphocytic leukemia (Small lymphocytic lymphoma may be included)

• Evidence of cerebral or meningeal involvement by lymphoma

• Patients without bi-dimensionally measurable disease

• ECOG performance status > 2

• Life expectancy less than 3 months

• Chemotherapy or radiation therapy or other investigational agents within 4 weeks prior to entering the study

• Previous radioimmunotherapy within 12 weeks

• Known anaphylaxis to infused proteins

• HIV, HBV and HCV positivity

• Poor kidney, liver and bone marrow functions

• Any serious active disease or co-morbid condition, which, in the opinion of the principle investigator, will interfere with the safety or the compliance with the study

• Pregnant or breast-feeding women

• Patients with reproductive potential without effective birth control methods

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.