Phase II Study of BI 2536 in Prostate Cancer

Inclusion Criteria

• •Male patient age \>18 years.
• •Signed informed consent.
• •Able to comply with protocol requirements.
• •Patients with histologically, cytologically or biochemically documented metastatic adenocarcinoma of the prostate, clinically refractory or resistant to hormone therapy, as documented by progression following at least one hormonal therapy, which must include orchidectomy or gonadotropin releasing hormone agonist (GnRHa).
• •Patients with Progressive Disease (PD). PD is defined as a minimum of three consecutive serum PSA measurements obtained at least 7 days apart within the previous 3 months of start of trial, which document progressively increasing PSA values. Patients with progression of measurable disease (RECIST) or progression of bone disease must also fit the criterion for PSA progression.
• •Patients must have documented progression (as defined above) following anti-androgen withdrawal of 4 weeks duration for flutamide and 6 weeks for bicalutamide or nilutamide. For a patient who has withdrawn from anti-androgen therapy less than 6 months prior to inclusion in the trial, one of the following criteria is also required:
• •Following completion of the anti-androgen withdrawal period one PSA measurement should be higher than the last pre-withdrawal PSA.
• •Or
• •Following the completion of the anti-androgen withdrawal period if the PSA value has decreased, a patient can still qualify if 2 increases in PSA are documented after the post- withdrawal nadir.
• •PSA \> 10 ng/ml.
• •A predicted life expectancy of at least 12 weeks.
• •A maximum of one prior treatment with either chemotherapy or other non-hormonal treatment modality.
• •ECOG performance status 0-1.
• •Stable analgesia requirements.
• •INR Prothrombin time (PT) and partial thromboplastin time (PTT) \<1.5 upper limit of normal.
• •Adequate bone marrow function defined as absolute neutrophil count (ANC) \> 1.5 x 109l, Platelet count \> 100 x 109/l.
• •Haemoglobin \> 9.0 mg/dl.
• •Serum Albumin \> 2.0 g/l.
• •Castrate testosterone level \[\< 20 ng/dl or \<0.69nM (nM/L x 28.8 = ng/dl)\] must be maintained during the duration of the trial by orchidectomy or medical castration.
• •Patients on oral or intravenous bisphosphonates are allowed to enter the trial as long as they have been on bisphosphonates for a minimum of 3 months.