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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00273936
Other study ID # AVN-944-002
Secondary ID
Status Completed
Phase Phase 1
First received January 6, 2006
Last updated August 2, 2011
Start date January 2006

Study information

Verified date August 2011
Source Vertex Pharmaceuticals Incorporated
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the safety and maximum tolerated dose, pharmacokinetics, and anti-neoplastic response of AVN-944 in patients with advanced hematologic malignancies.


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Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label


Intervention

Drug:
AVN-944 capsules for oral administration


Locations

Country Name City State
United States Ohio State University, James Cancer Hospital Comprehensive Cancer Center Columbus Ohio
United States Oregon Health and Science University Portland Oregon
United States Stanford Cancer Center Stanford California
United States Arizona Clinical Research Center Tucson Arizona
United States George Washington University Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Vertex Pharmaceuticals Incorporated

Country where clinical trial is conducted

United States, 

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