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Completed Phase 3 Interventional Results available

Study of the Combination of Rituximab, Cyclophosphamide, Doxorubicin, VELCADE, and Prednisone or Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone in Patients With Newly Diagnosed Mantle Cell Lymphoma

ClinicalTrials.gov ID: NCT00722137

Public ClinicalTrials.gov record NCT00722137. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 7:24 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open-Label, Multicenter Phase 3 Study of the Combination of Rituximab, Cyclophosphamide, Doxorubicin, VELCADE, and Prednisone (VcR-CAP) or Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) in Patients With Newly Diagnosed Mantle Cell Lymphoma Who Are Not Eligible for a Bone Marrow Transplant

Study identification

NCT ID
NCT00722137
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Millennium Pharmaceuticals, Inc.
Industry
Enrollment
487 participants

Conditions and interventions

Interventions

  • Rituximab 375 mg/m^2 Drug
  • Cyclophosphamide 750 mg/m^2 Drug
  • Doxorubicin 50 mg/m^2 Drug
  • VELCADE 1.3 mg/m^2 Drug
  • Prednisone 100 mg/m^2 Drug
  • Vincristine 1.4 mg/m^2 Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2008
Primary completion
Dec 31, 2013
Completion
Jun 16, 2017
Last update posted
Jul 11, 2018

2008 – 2017

United States locations

U.S. sites
9
U.S. states
9
U.S. cities
9
Facility City State ZIP Site status
St. Francis Hosptial and Medical Center Hartford Connecticut 06105
Center for Cancer Care at Goshen Hospital Goshen Indiana 46526
Sinai Hospital Baltimore Maryland 21215
Capitol Comp. Cancer Center Jefferson City Missouri 65109
Nebraska Cancer Specialists Omaha Nebraska 68114
Hematology-Oncology Associates of Northern NJ Morristown New Jersey 07960
Legacy Pharma Research Bismarck North Dakota 58501
Division of Hematology and Oncology Vanderbilt University Nashville Tennessee 37232
Cancer Outreach Associates, PC Abingdon Virginia 24211

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 141 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00722137, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 11, 2018 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00722137 live on ClinicalTrials.gov.

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