Status:
COMPLETED
Phase I of BIBW 2992/BIBF 1120 Combination Therapy in Solid Tumors
Lead Sponsor:
Boehringer Ingelheim
Conditions:
Neoplasms
Eligibility:
All Genders
18-75 years
Phase:
PHASE1
Brief Summary
The primary objective of this trial is to determine the MTD of the combination of BIBW 2992/BIBF 1120 therapy administered concomitantly in a 28-day cycle schedule. Secondary objectives are the colle...
Eligibility Criteria
Inclusion
- Male or female patients with confirmed diagnosis of advanced, non-resectable and/or metastatic solid tumors, who have failed conventional treatment, or for whom no therapy of proven efficacy exists, or who are not amenable to established forms of treatment.
- Age 18 years or older.
- Life expectancy of at least three (3) months.
- Written informed consent that is consistent with ICH-GCP guidelines.
- Eastern Cooperative Oncology Group performance score 0, 1or 2.
- Patients recovered from any therapy-related toxicities from previous chemo-,hormone-, immuno-, or radiotherapies to CTC \<= Grade 1.
- Patients must have recovered from previous surgery.
Exclusion
- Active infectious disease.
- Gastrointestinal disorders that may interfere with the absorption of the study drug or chronic diarrhea.
- Serious illness or concomitant non-oncological disease considered by the investigator to be incompatible with the protocol.
- Patients with untreated or symptomatic brain metastases. Patients with treated, asymptomatic brain metastases are eligible if there has been no change in brain disease status for at least four (4) weeks, no history of cerebral edema or bleeding in the past four (4) weeks and no requirement for steroids or anti-epileptic therapy.
- Cardiac left ventricular function with resting ejection fraction \<50%.
- Absolute neutrophil count (ANC) less than 1500/mm3.
- Platelet count less than 100,000/mm3.
- Bilirubin greater than 1.5 mg/dl (\>26 ¿mol /L, SI unit equivalent).
- Aspartate amino transferase (AST) or alanine amino transferase (ALT) greater than two and a half times the upper limit of normal (2.5 X ULN ).
- Serum creatinine greater than 1.5 mg/dl (\>132 ¿mol/L, SI unit equivalent).
- Women and men who are sexually active and unwilling to use a medically acceptable method of contraception.
- Pregnancy or breast-feeding.
- Treatment with other investigational drugs; chemotherapy, immunotherapy, radiotherapy or hormone therapy (including LHRH agonists, megestrol acetate, or other hormones taken for breast cancer or prostate cancer); participation in another clinical study within the past 4 weeks before start of therapy or concomitantly with this study. Treatment with bisphosphonates is allowed.
- Treatment with an EGFR- or HER2 inhibiting drug within the past 4 weeks before start of therapy or concomitantly with this study (2 weeks for trastuzumab).
- Patients unable to comply with the protocol.
- Active alcohol or drug abuse.
- Patients who require therapeutic anticoagulation or antiplatelet therapy \[except treatment with Aspirin (Acetylsalicylic Acid)\].
- Patients with history of haemorrhagic or thrombotic events (including transient ischemic attacks) in the past 12 months. Known inherited predisposition to bleeding or thrombosis.
Key Trial Info
Start Date :
January 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
28 Patients enrolled
Trial Details
Trial ID
NCT00730821
Start Date
January 1 2007
Last Update
August 21 2009
Active Locations (4)
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1
1239.1.3 Boehringer Ingelheim Investigational Site
Scottsdale, Arizona, United States
2
1239.1.1 Boehringer Ingelheim Investigational Site
Tampa, Florida, United States
3
1239.1.2 Boehringer Ingelheim Investigational Site
Detroit, Michigan, United States
4
1239.1.4 Boehringer Ingelheim Investigational Site
Omaha, Nebraska, United States