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Completed Phase 1Phase 2 Interventional Results available

Study Evaluating Inotuzumab Ozogamicin [CMC-544] Administered In Combination With Rituximab In Subjects With Non-Hodgkin's Lymphoma (NHL)

ClinicalTrials.gov ID: NCT00299494

Public ClinicalTrials.gov record NCT00299494. 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 Sep 7, 2026, 9:14 AM 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 Phase 1/2 Study Of Cmc-544 Administered In Combination With Rituximab In Subjects With Follicular Or Diffuse Large B-cell Non-hodgkin's Lymphoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to determine the tolerability, the initial safety profile and maximum tolerated dose, and to obtain preliminary information on the antitumor activity of inotuzumab ozogamicin \[CMC-544\] in combination with rituximab in subjects with follicular, diffuse large B-Cell, or mantle cell NHL.

Study identification

NCT ID
NCT00299494
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
119 participants

Conditions and interventions

Interventions

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
May 3, 2006
Primary completion
May 18, 2014
Completion
Jun 1, 2014
Last update posted
Mar 7, 2018

2006 – 2014

United States locations

U.S. sites
19
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
University of Alabama at Birmingham- Birmingham Alabama 35249 - 3300
IDS Pharmacy Birmingham Alabama 35249
University of Alabama at Birmingham- Birmingham Alabama 35294
California Cancer Care, Inc. Greenbrae California 94904
University of California Medical Center San Francisco California 94143
California Cancer Care San Mateo California 94402
Emory Clinic Atlanta Georgia 30322
Emory University Hospital Atlanta Georgia 30322
Emory University Investigational Drug Service Atlanta Georgia 30322
Northwestern Medical Faculty Foundation Chicago Illinois 60611
Nevada Cancer Institute- Las Vegas Nevada 89135
Rosewell Park Cancer Institute Buffalo New York 14263
Gabrail Cancer Center Canton Ohio 44718
University Hospitals of Cleveland Cleveland Ohio 44106
Cleveland Clinic Cleveland Ohio 44195
Gabrail Cancer Center Dover Ohio 44622
UHHS - Westlake Westlake Ohio 44145
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
The University of Texas M.D. Anderson Cancer Center Houston Texas 77030-4009

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 19 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00299494, 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 Mar 7, 2018 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00299494 live on ClinicalTrials.gov.

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