Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00073957 · ClinicalTrials.gov registry record · Phase 2

Y 90 Ibritumomab Tiuxetan &Rituximab Relapsed or Refractory Diffuse Large B-Cell Non-Hodgkin's Lymphoma

A Phase 2 study of Lymphoma, sponsored by Beth Israel Deaconess Medical Center.

Completed
Registry status
Phase 2
Development phase
25
Enrollment target
2
Study locations

NCT00073957: Completed Phase 2 study of Lymphoma, sponsored by Beth Israel Deaconess Medical Center.

NCT00073957 is a Phase 2 study of Lymphoma that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 25 participants, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (95% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00073957, a Phase 2 study of Lymphoma, has completed, sponsored by Beth Israel Deaconess Medical Center.

COMPLETED
Registry status
Phase 2
Development phase
25 participants
Enrollment target
2
Study locations

Study Summary

RATIONALE: Monoclonal antibodies, such as yttrium Y 90 ibritumomab tiuxetan and rituximab, can locate cancer cells and either kill them or deliver radioactive cancer-killing substances to them without harming normal cells. Combining yttrium Y 90 ibritumomab tiuxetan with rituximab may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of combining yttrium Y 90 Ibritumomab tiuxetan with rituximab in treating patients who have relapsed or refractory diffuse large B-cell non-Hodgkin's lymphoma.

Primary Outcome

Definition Nodal Masses Spleen, Liver Bone Marrow CR Disappearance of all evidence of disease Partial response Regression and no new sites ≥ 50% decrease in sum of the perpendicular dimension of up to 6 largest dominant masses; no increase in size of other nodes Stable disease Failure to attain CR/PR or Progressive disease or Relapsed disease : the appearance of any new lesion or the (a) FDG-avid or PET positive prior to therapy; PET positive at prior sites of disease and no new sites on CT or P

Conditions Studied

Interventions

  • BIOLOGICAL rituximab
  • DRUG cytarabine
  • DRUG liposomal cytarabine
  • RADIATION yttrium Y 90 ibritumomab tiuxetan

Study Locations (2)

Massachusetts

  • Beth Israel Deaconess Medical Center - Boston

Vermont

  • Fletcher Allen Health Care - Medical Center Campus - Burlington

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2003-12
Est. Completion 2012-01-01
Phase Phase 2

What the finished NCT00073957 record still lists

NCT00073957 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (95% lower).

The record links to 1 condition, with Lymphoma appearing as the primary indexed condition, and to 4 interventions - of which rituximab is the first listed.

NCT00073957 reports a single indexed study location in Massachusetts, Vermont.

Frequently Asked Questions

What is clinical trial NCT00073957 about?

NCT00073957 is a clinical study titled "Y 90 Ibritumomab Tiuxetan &Rituximab Relapsed or Refractory Diffuse Large B-Cell Non-Hodgkin's Lymphoma". RATIONALE: Monoclonal antibodies, such as yttrium Y 90 ibritumomab tiuxetan and rituximab, can locate cancer cells and either kill them or deliver radioactive cancer-killing substances to them without harming normal cells. Combining yttrium Y 90 ibritumomab tiuxetan with rituximab may kill more canc...

What is the current status of trial NCT00073957?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 25 participants. The study started on 2003-12. Estimated completion is 2012-01-01.

What conditions does trial NCT00073957 study?

This clinical trial studies the following conditions: Lymphoma.

What interventions are being tested in trial NCT00073957?

The interventions under investigation include: rituximab (BIOLOGICAL), cytarabine (DRUG), liposomal cytarabine (DRUG), yttrium Y 90 ibritumomab tiuxetan (RADIATION).

Who is sponsoring clinical trial NCT00073957?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00073957 being conducted?

This trial has 2 study locations across Massachusetts, Vermont. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Lymphoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00073957's enrollment target sits among peer trials

25 230th of 299 higher than 66 of 299 other Lymphoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Lymphoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01166854 · 25 participants

    Characterization of Familial Myopathy and Paget Disease of Bone

  • NCT01913106 · 25 participants · Phase 1

    HSV-tk + Valacyclovir Therapy in Combination With Brachytherapy for Recurrent Prostate Cancer

  • NCT02138669 · 25 participants · NA

    Intacs Prescription Inserts for Keratoconus Patients

  • NCT02174549 · 25 participants · Phase 1

    Dose-defining Study of Tirapazamine Combined With Embolization in Liver Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00073957, the US trial registry maintained by the National Library of Medicine. NCT00073957 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.