Treatment of Non-Hodgkin's Lymphoma With 90Y-hLL2 IgG

NCT00061425 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL

Last updated 2021-08-19

No results posted yet for this study

Summary

The purpose of this trial is to determine the safety of a 90Y-radiolabeled, humanized (CDR-grafted) form of the LL2 monoclonal antibody in patients with Non-Hodgkin's lymphoma (NHL) at different dose levels.

Conditions

  • Non-Hodgkin's Lymphoma
  • Lymphoma, B-Cell

Interventions

DRUG

radiolabeled epratuzumab

Sponsors & Collaborators

Principal Investigators

  • William Wegener · Gilead Sciences

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-08-31
Primary Completion
2007-11-30

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00061425 on ClinicalTrials.gov