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Completed Phase 2 Interventional

Study of Talabostat and Rituximab in Advanced Chronic Lymphocytic Leukemia (CLL)

ClinicalTrials.gov ID: NCT00086203

Public ClinicalTrials.gov record NCT00086203. 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 10, 2026, 8:09 AM EDT

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

Brief summary

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

The objective of this study is to assess the efficacy and safety of talabostat and rituximab in patients with advanced CLL who failed to respond, or have progressed following a prior response, to a fludarabine regimen.

Study identification

NCT ID
NCT00086203
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Point Therapeutics
Industry
Enrollment
Not listed

Conditions and interventions

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
Not listed
Primary completion
Not listed
Completion
Aug 31, 2007
Last update posted
Mar 24, 2015

Ends 2007

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
University of Arkansas for Medical Science Little Rock Arkansas 72205
Ocala Oncology Center Ocala Florida 34474
Gulfcoast Oncology Associates St. Petersburg Florida 33705
Indiana Oncology/Hematology Consultants Indianapolis Indiana 46202
Dana Farber Cancer Institute Boston Massachusetts 02115
Hematology/Oncology Centers of the Northern Rockies Billings Montana 59101
Nevada Cancer Institute Las Vegas Nevada 89135
Queens Medical Associates, PC Fresh Meadows New York 11365
Long Island Jewish Medical Center New Hyde Park New York 11040
NYU Medical Center New York New York 10016
James P. Wilmot Cancer Center/University of Rochester Rochester New York 14642
Raleigh Hematology/Oncology Clinic Cary North Carolina 27511
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
Cancer Care Associates/Oklahoma City Oklahoma City Oklahoma 73112
Cancer Care Associates--Tulsa Tulsa Oklahoma 74136
Cancer Centers of the Carolinas Seneca South Carolina 29672
Texas Cancer Center/Abilene Abilene Texas 79606-5208
MD Anderson Cancer Center Houston Texas 77030
Virginia Oncology Associates-Lake Wright Cancer Center Norfolk Virginia 23502

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00086203, 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 24, 2015 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00086203 live on ClinicalTrials.gov.

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