Prostate Cancer Clinical Trial

Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exhibiting Early Signs of Biochemical Failure

Summary

The purpose of this phase II, randomized, double-blind placebo controlled, multi-center study is to evaluate the safety and efficacy of 10 mg atrasentan in hormone naive subjects as measured by rate of rise in the PSA (primary objective).

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

prostate adenocarcinoma,
radical prostatectomy,
PSA between 0.4 and 5 ng/mL,
PSADT < 1 year

Exclusion Criteria:

previous hormonal therapy,
salvage therapy to the pelvis within 3 months prior to randomization

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

200

Study ID:

NCT00038662

Recruitment Status:

Completed

Sponsor:

Abbott

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There are 39 Locations for this study

See Locations Near You

Urology Centers Of Alabama
Homewood, Alabama, 35205, United States
Alaska Clinical Research Center, LLC
Anchorage Alaska, 99508, United States
Arkansas Urologial Associates, PA
Little Rock Arkansas, 72205, United States
San Diego Urology Center
La Mesa California, 91942, United States
Western Clinical Research Inc
Torrance California, 90505, United States
Georgetown University Medical Center
Washington District of Columbia, 20007, United States
Clinical Physiology Associates
Fort Myers Florida, 33916, United States
Southeastern Urological Center, PA
Tallahassee Florida, 32308, United States
Northwestern University
Chicago Illinois, 60611, United States
Johns Hopkins Oncology Center
Baltimore Maryland, 21231, United States
Sheldon Freedman MD
Las Vegas Nevada, 89109, United States
VA Medical Center(111)
Reno Nevada, 89502, United States
Nevada Urology Associates
Reno Nevada, 89511, United States
Carolinas Medical Centre
Charlotte, North Carolina, 28204, United States
Cleveland Clinic Foundation
Cleveland Ohio, 44195, United States
Urologic Specialists Of Oklahoma, Inc.
Tulsa, Oklahoma, 74104, United States
Oregon Urology Specialists
Eugene Oregon, 97401, United States
Urological Assoc. of Lancaster
Lancaster Pennsylvania, 17604, United States
University Of Pittsburgh
Pittsburgh Pennsylvania, 15232, United States
Center for Urologic Care
West Reading, Pennsylvania, 19611, United States
Center for Urologic Care
West Reading Pennsylvania, 19611, United States
Ntouch Research Corporation
Dallas Texas, 75230, United States
Salt Lake Research
Salt Lake City Utah, 84124, United States
Jeffrey Frankel, M.D.
Seattle, Washington, 98166, United States
University of Washington Medical Center
Seattle Washington, 98195, United States
Tom Baker Cancer Center
Calgary, Alberta, T2N 4, Canada
Cross Cancer Institute
Edmonton Alberta, T6G1Z, Canada
Cal Andreou, MD
Surrey British Columbia, V3V 1, Canada
Can-Med Medical Research Inc
Victoria British Columbia, , Canada
Bruce W. Palmer Urology Inc.
Kentville Nova Scotia, B4N4K, Canada
The Male Health Centres
Barrie Ontario, L4M 4, Canada
Burlington Professional Centre
Burlington Ontario, L7N 3, Canada
Hamilton & District Urology Association
Hamilton, Ontario, L8N 1, Canada
London Health Sciences Centre
London Ontario, N6A 4, Canada
Quest Clinical Trials
Markham Ontario, L6B1A, Canada
Guardian Medical Arts Bldg.
North Bay Ontario, P1B4Z, Canada
Jack Barkin, MD
North York Ontario, M6A 3, Canada
The Male Health Centres
Oakville Ontario, L6H 3, Canada
Sunnybrook &Women's College Health Sciens Center
Toronto Ontario, M4N 3, Canada
Hopital Notre-Dame
Montreal Quebec, H2L 4, Canada
Chuq Pavillon Hotel-Dieu
Quebec , G1R 2, Canada

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

200

Study ID:

NCT00038662

Recruitment Status:

Completed

Sponsor:


Abbott

How clear is this clinincal trial information?

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