A Study With BIBF 1120 in Patients With Hormone Refractory Prostate Cancer
NCT ID: NCT02182063
Last Updated: 2017-12-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
81 participants
INTERVENTIONAL
2005-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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BIBF 1120 low dose
BIBF 1120 low dose
BIBF 1120 high dose
BIBF 1120 high dose
Interventions
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BIBF 1120 low dose
BIBF 1120 high dose
Eligibility Criteria
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Inclusion Criteria
2. Presence of histologically documented adenocarcinoma of the prostate
3. Presence of metastatic disease
4. Life expectancy of at least 3 months
5. Progression after orchidectomy or during LH-RH (Luteinising hormone - releasing hormone) analogs with castrate testosterone serum levels \<30 ng/ml (chemical castration had to be continued) and absence of anti-androgen withdrawal syndrome
6. Minimum value of PSA = 20 ng/ml at screening
7. Stopping the previous treatment with docetaxel based regimen or/and with antiandrogen 4 weeks before the inclusion of the patient
8. ECOG performance status ≤ 2
9. Progression after only one previous chemotherapy with docetaxel based regimen:
* Appearance of a new lesion or increase of an existing measurable / non measurable lesion
* Increase of PSA ≥ 25% documented by two successive exams
* Increase of pain if there is a correlation with a radiological progression or with a PSA increase as defined above
10. Adequate hepatic function: total bilirubin within normal limits, ALT (Alanine aminotransferase) and/or AST (aspartate aminotransferase) ≤ 1.5x upper limit of normal (ULN). Prothrombin time (PT) and partial thromboplastin time (PTT): maximum 50% deviation from normal limits
11. Adequate renal function: serum creatinine ≤ 2 x upper normal limit (UNL)
12. Absolute neutrophil count (ANC) ≥ 1500/mL, Platelets ≥ 100,000/mL, Hemoglobin ≥ 9.0 g/dL (hemoglobin may be supported by transfusion or erythropoietin or other approved hematopoietic growth factors)
Exclusion Criteria
2. Serious illness or concomitant non-oncological disease such as neurologic-, psychiatric-, infectious disease or active ulcers (gastro-intestinal tract, skin) or laboratory abnormality that may increase the risk associated with study participation or study drug administration and in the judgment of the investigator would make the patient inappropriate for entry into the study
3. Significant cardiovascular diseases (i.e. uncontrolled hypertension, instable angina, history of myocardial infarction or congestive heart failure \>NYHA II (New York Heart Association) during the 6 previous months
4. Strontium or equivalent radioactive isotope during the 6 previous months
5. Concomitant second malignancy, with the exception of treated basal cell carcinoma of the skin or a recovered cancer at least since 5 years
6. Major injuries and surgeries within the past 4 weeks. Planned surgical procedures during the trial. Patients with incomplete wound healing
7. History of haemorrhagic or emerging thrombotic event. Known inherited predisposition to hemorrhage or thrombosis
8. Patients who require full-dose anticoagulation or heparinization or continuous treatment with acetylsalicyclic acid \> 325 mg
9. Concomitant treatment with other experimental drugs or anti-cancer therapy including hormone therapy (except LH-RH agonists)
10. Biphosphonates during the study since four weeks prior to the inclusion of the patient
11. Known or suspected symptomatic brain metastases
12. Known or suspected symptomatic epiduritis
13. Treatment with other investigational drugs or participation in another clinical trial within the past four weeks before start of therapy (visit 2) or concomitantly with this trial
14. Patients unable to comply with the protocol
MALE
No
Sponsors
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Boehringer Ingelheim
INDUSTRY
Responsible Party
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Related Links
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Related Info
Other Identifiers
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1199.11
Identifier Type: -
Identifier Source: org_study_id