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Brief Title: ZK-Epo Given With Carboplatin in Patients With Recurrent Ovarian Cancer
Official Title: Phase 1/2 Study of ZK-Epothilone (ZK-Epo; ZK-219477) in Combination With Carboplatin in Patients With Platinum-sensitive Recurrent Ovarian Cancer
Study ID: NCT00325351
Brief Summary: The purpose of this study is to evaluate whether treatment with a new drug called ZK-Epothilone (ZK-Epo) given with carboplatin in patients with recurrent ovarian cancer, who previously have had a good response with cisplatin or carboplatin, is safe and helps to decrease or stop tumor growth.
Detailed Description: This study has previously been registered by Berlex, Inc. Berlex, Inc. has been renamed to Bayer HealthCare Pharmaceuticals, Inc.Bayer HealthCare Pharmaceuticals, Inc. is sponsoring this trial.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
, Tucson, Arizona, United States
, Little Rock, Arkansas, United States
, Bakersfield, California, United States
, La Jolla, California, United States
, San Diego, California, United States
, Savannah, Georgia, United States
, South Bend, Indiana, United States
, Baltimore, Maryland, United States
, Albuquerque, New Mexico, United States
, Winston-Salem, North Carolina, United States
, Cleveland, Ohio, United States
, Oklahoma City, Oklahoma, United States
, Knoxville, Tennessee, United States
, Roanoke, Virginia, United States
, Calgary, Alberta, Canada
, Toronto, Ontario, Canada
Name: Bayer Study Director
Affiliation: Bayer
Role: STUDY_DIRECTOR