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Completed Phase 2 Interventional

Alvocidib in Patients With Previously Treated Chronic Lymphocytic Leukemia or Prolymphocytic Leukemia Arising From Chronic Lymphocytic Leukemia (CLL)

ClinicalTrials.gov ID: NCT00464633

Public ClinicalTrials.gov record NCT00464633. 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 Jul 23, 2026, 1:26 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 Multicenter, Open-label, Single Arm Study of Weekly Alvocidib in Patients With Previously Treated B-Cell Chronic Lymphocytic Leukemia (CLL) or Prolymphocytic Leukemia (PLL) Arising From CLL

Study identification

NCT ID
NCT00464633
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sanofi
Industry
Enrollment
165 participants

Conditions and interventions

Interventions

  • alvocidib 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
Feb 28, 2007
Primary completion
Nov 30, 2011
Completion
Nov 30, 2011
Last update posted
Feb 11, 2013

2007 – 2011

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
Sanofi-Aventis Investigational Site Number 840008 San Diego California 92103
Sanofi-Aventis Investigational Site Number 840022 San Francisco California 94143
Sanofi-Aventis Investigational Site Number 840010 Chicago Illinois 60611
Sanofi-Aventis Investigational Site Number 840012 Chicago Illinois 60637
Sanofi-Aventis Investigational Site Number 840017 Indianapolis Indiana 46202
Sanofi-Aventis Investigational Site Number 840001 Boston Massachusetts 02115
Sanofi-Aventis Investigational Site Number 840023 Ann Arbor Michigan 48109-0759
Sanofi-Aventis Investigational Site Number 840005 New York New York 10021
Sanofi-Aventis Investigational Site Number 840006 New York New York 10029-6574
Sanofi-Aventis Investigational Site Number 840003 Durham North Carolina 27710
Sanofi-Aventis Investigational Site Number 840018 Cleveland Ohio 44106
Sanofi-Aventis Investigational Site Number 840002 Columbus Ohio 43210
Sanofi-Aventis Investigational Site Number 840020 Philadelphia Pennsylvania 19104

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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00464633, 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 Feb 11, 2013 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00464633 live on ClinicalTrials.gov.

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