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COMPLETED Phase 2

VELCADE® (Bortezomib) With Rituximab in Subjects With Relapsed or Refractory Indolent B-Cell Lymphoma

NCT00085696 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the safety and effectiveness of VELCADE when given in combination with rituximab in patients with Relapsed or Refractory Indolent B-Cell Lymphoma. This study will investigate if treatment with VELCADE and rituximab increases the time it takes your lymphoma to get worse.

Interventions

  • DRUG VELCADE and rituximab

Study Locations (13)

Georgia

  • Emory University Cancer Institute, Winship Cancer Institute — Atlanta
  • Georgia Cancer Specialists — Marietta

Illinois

  • Rush University Medical Center — Chicago
  • Midwest Cancer Research Group — Skokie

California

  • UCLA School of Medicine — Los Angeles

Florida

  • Florida Cancer Specialists — Fort Myers

Kansas

  • Cancer Center of Kansas — Wichita

Missouri

  • Oncology/Henmatology Associates of Kansas City — Kansas City

Ohio

  • Mid Ohio Oncology/Hematology Inc. — Columbus

South Carolina

  • Charleston Cancer Center — Charleston

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2004-05
Phase Phase 2

Sponsor

Millennium Pharmaceuticals

21 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00085696

The ClinicalTrials.gov registry entry for NCT00085696 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 66 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Millennium Pharmaceuticals, which has 21 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Follicular Lymphoma appearing as the primary indexed condition, and to 1 intervention — of which VELCADE and rituximab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00085696 reports 13 study locations spanning 11 distinct geographic areas — top geographies include Georgia, Illinois, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00085696 about?

NCT00085696 is a clinical study titled "VELCADE® (Bortezomib) With Rituximab in Subjects With Relapsed or Refractory Indolent B-Cell Lymphoma". The purpose of this study is to evaluate the safety and effectiveness of VELCADE when given in combination with rituximab in patients with Relapsed or Refractory Indolent B-Cell Lymphoma. This study will investigate if treatment with VELCADE and rituximab increases the time it takes your lymphoma to...

What is the current status of trial NCT00085696?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 66 participants. The study started on 2004-05.

What conditions does trial NCT00085696 study?

This clinical trial studies the following conditions: Follicular Lymphoma, B-Cell Lymphoma, Marginal Lymphoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00085696?

The interventions under investigation include: VELCADE and rituximab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00085696?

This trial is sponsored by Millennium Pharmaceuticals, which has 21 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00085696 being conducted?

This trial has 13 study locations across California, Florida, Georgia, Illinois, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial