CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 12 enrolled
Drug / intervention
Rituximab +1 moredrug
Likely dose
Rituximab 250 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00387023
NCT00387023N/ACompleted

Pilot Trial of Radioimmunotherapy With Yttrium 90-Labeled (90Y) Zevalin for Low-Grade Follicular Non-Hodgkin's Lymphoma or MALT of the Orbit/Conjunctiva

M.D. Anderson Cancer Center·interventional·Posted Oct 12, 2006·Updated Nov 18, 2013

In Brief

A clinical study evaluating Rituximab and Zevalin for Non-Hodgkin's Lymphoma and Lymphoma. Completed, enrolled 12 participants across 1 site.

Detailed Summary

Primary Objectives: 1. To evaluate the efficacy of Zevalin for the treatment of low-grade follicular Non-Hodgkin's lymphoma of the orbit or mucosa-associated lymphoid tissue (MALT) of conjunctiva using radiographic imaging, clinical examination (slit lamp biomicroscopy and external examination of the conjunctiva), and external photography whenever possible. 2. To establish the safety profile in this patient population using clinical examination including slit lamp biomicroscopy, and evaluation of the tear film with Schirmer's test. 3. To establish the dosimetry for Zevalin in the orbit in the first 3 patients who agree to undergo dosimetry.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsBiogen

Timeline

N/ACompletedFinished
200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 12, 2006
Enrollment StartFeb 1, 2004
Primary CompletionJul 1, 2012
TodayJul 2, 2026
Enrollment to primary: 8.4 yearsPosted 19.7 years ago

Interventions

Rituximabdrug

250 mg/m\^2 IV over 4-6 hours for 2 weeks.

Zevalindrug

5 mCi/kg IV over 30 minutes for 1 week, followed by 0.3 mCi/kg or 0.4 mCi/kg 90Y-Zevalin based on platelet counts for 1 week.