Spots Global Cancer Trial Database for Safety of LBH589 Alone and in Combination With Intravenous Docetaxel and Prednisone
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Trial Identification
Brief Title: Safety of LBH589 Alone and in Combination With Intravenous Docetaxel and Prednisone
Official Title: A Phase IA/IB, Two Arm, Multi-center, Open-label, Dose Escalation Study of Oral LBH589 Alone and in Combination With IV Docetaxel and Oral Prednisone in Hormone Refractory Prostate Cancer (HRPC)
Study ID: NCT00419536
Interventions
Study Description
Brief Summary: This 2-arm study is designed to determine the maximum tolerated dose of LBH589 as a single agent and in combination with docetaxel and prednisone 5 mg twice daily (second arm) and to characterize the safety, tolerability, biologic activity and pharmacokinetic profile.
Detailed Description:
Keywords
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: MALE
Healthy Volunteers: No
Locations
Dana Farber Cancer Institute, Boston, Massachusetts, United States
Washington University School of Medicine, St. Louis, Missouri, United States
Memorial Sloan Kettering Cancer Center, New York, New York, United States
Contact Details
Name: Novartis Pharmaceuticals
Affiliation: Novartis Pharmaceuticals
Role: STUDY_DIRECTOR
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