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

NCT01510184 · ClinicalTrials.gov registry record · Phase 3

Study of Zevalin Versus Observation in Participants at Least 60 Years Old With Newly Diagnosed Diffuse Large B-cell Lymphoma in Positron Emission Tomography (PET)-Negative Complete Remission After Rituximab-Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) or R-CHOP-like Therapy

A Phase 3 study, sponsored by Spectrum Pharmaceuticals.

Terminated
Registry status
Phase 3
Development phase
79
Enrollment target

NCT01510184: Clinical Trial Phase 3 study, sponsored by Spectrum Pharmaceuticals.

NCT01510184 is a Phase 3 study that was terminated before completion, run by Spectrum Pharmaceuticals. The registered enrollment target is 79 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01510184, a Phase 3 study, was terminated before completion, sponsored by Spectrum Pharmaceuticals.

TERMINATED
Registry status
Phase 3
Development phase
79 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the efficacy and safety of Zevalin compared with observation alone in participants who are in PET-negative complete remission after first-line R-CHOP or R-CHOP like therapy.

Primary Outcome

OS was the time from randomization to death. In living participants, survival time was censored on the last date that participants were known to be alive. OS for living participant was calculated as (end of study date/last visit date - randomization date)+ 1/30.4375. Overall Survival was summarized separately for living participants as only few participants died in this study.

Interventions

  • DRUG Rituximab
  • DRUG Zevalin
  • DRUG Y-90-Zevalin
  • DRUG In-111 Zevalin

Trial Details

FieldValue
Enrollment Target 79 participants
Start Date 2012-04-19
Est. Completion 2014-10-23
Phase Phase 3
Spectrum Pharmaceuticals

52 total trials

Why NCT01510184 stopped before completion

NCT01510184 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 79 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 4 interventions - of which Rituximab is the first listed.

NCT01510184 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01510184 about?

NCT01510184 is a clinical study titled "Study of Zevalin Versus Observation in Participants at Least 60 Years Old With Newly Diagnosed Diffuse Large B-cell Lymphoma in Positron Emission Tomography (PET)-Negative Complete Remission After Rituximab-Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) or R-CHOP-like Therapy". The purpose of this study is to evaluate the efficacy and safety of Zevalin compared with observation alone in participants who are in PET-negative complete remission after first-line R-CHOP or R-CHOP like therapy.

What is the current status of trial NCT01510184?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 79 participants. The study started on 2012-04-19. Estimated completion is 2014-10-23.

What interventions are being tested in trial NCT01510184?

The interventions under investigation include: Rituximab (DRUG), Zevalin (DRUG), Y-90-Zevalin (DRUG), In-111 Zevalin (DRUG).

Who is sponsoring clinical trial NCT01510184?

This trial is sponsored by Spectrum Pharmaceuticals, which has 52 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01510184's enrollment target sits among peer trials

79 1768th of 2000 higher than 232 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

  • NCT05798897 · 79 participants · Phase 1

    Safety and Preliminary Efficacy of MT-601 in Patients With Relapsed/Refractory Lymphoma

  • NCT06042439 · 79 participants · NA

    AM vs PM Exercise Training

  • NCT06223555 · 79 participants · NA

    Variability In Mixed Meal Tests: Fixed Versus Adjusted to Energy Needs Caloric Dose

  • NCT01243931 · 80 participants · NA

    Optical Coherence Tomography Guided Transepithelial Phototherapeutic Keratectomy

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01510184, the US trial registry maintained by the National Library of Medicine. NCT01510184 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.