Solid Tumors
Conditions
Brief summary
To determine the maximum tolerated dose (MTD) and dose limiting toxicities (DLTs) of ABI-009 given weekly; to characterize the toxicities of ABI-009; and to determine the pharmacokinetic parameters for ABI-009 when given on a weekly schedule.
Detailed description
No extended description necessary
Interventions
DRUGABI-009
nab-rapamycin
Sponsors
Celgene
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Each subject must meet the following criteria to be enrolled in this study. 1. Male and female patients with histologically or cytologically confirmed diagnosis of cancer which is not amenable to curative therapy. 2. Patients with advanced non-hematologic malignancies for whom no standard therapy exists. 3. Measurable disease by RECIST or evaluable disease (e.g., bone metastasis, pleural effusion, ascites, or lesions which do not fulfill RECIST criteria for metastatic disease) 4. Off all therapy (inclusive of investigational therapies) for at least 4 weeks prior to study drug administration OR off all daily or weekly therapy (inclusive of investigational therapies) for at least 2 weeks prior to study drug administration and without any side effects associated with these therapies. 5. Female patients of child-bearing potential must have a negative serum pregnancy test within 7 days prior to first study drug administration. 6. Female patients who are postmenopausal must have 12 months of amenorrhea, surgically sterile, or must agree to the use of a physical method of non-hormonal contraception. 7. Male patients must be surgically sterile or agree to the use of a barrier method of contraception. 8. Life expectancy of \> 3 months. 9. ECOG Performance Status of 0-1. 10. Patients must be able to provide informed consent indicating knowledge of his/her disease process, the investigational nature of the therapy, alternatives, benefits, and risks including potential side effects. 11. Age ≥ 18 years of age. 12. No major surgery within 4 weeks before treatment with ABI-009. (A biopsy is not considered major surgery). 13. No chemotherapy, hormonal therapy, immunotherapy or radiotherapy within 4 weeks before treatment with ABI-009 (6 weeks for previous treatment with nitrosoureas, mitomycin, or extensive radiotherapy) and no immunosuppressive agents within 3 weeks before study entry (except corticosteroids used as antiemetics). 14. No immunosuppressive agents within 3 weeks before study entry (except corticosteroids used as antiemetics). 15. Required Initial Laboratory Data: * Hemoglobin \> 9.0 g/dL * WBC ≥ 3,000/µl * ANC ≥ 1,500/µl * Platelet count ≥ 100,000/µl * Total Bilirubin ≤ ULN * SGOT (AST) SGPT (ALT) ≤ 1.5 x ULN ≤ 1.5 x ULN * Serum Cholesterol \< 350 mg/dL * Serum Triglyceride \< 300 mg/dL 16. Adequate renal function with serum creatinine \< 1.5 mg/dL and/or creatinine clearance (cockroft formula) ≥ 60 mL/min. 17. No active alcohol abuse, drug addiction, or psychotic disorders. 18. No known concomitant genetic or acquired immunosuppressive diseases (such as AIDS). 19. If obese, a patient must be treated with doses calculated using his/her actual BSA (The physician must be comfortable treating at the full BSA dose regardless of BSA).
Exclusion criteria
Subjects who meet any of the following criteria will be excluded from the study. 1. Pregnant or nursing women. 2. History of allergic reactions attributed to compounds of similar chemical or biologic composition including macrolide (e.g. azithromycin, clarithromycin, dirithromycin, and erythromycin) and ketolide antibiotics. 3. Patients have not recovered from adverse affects of radiation therapy or investigational agent within previous 28 days. 4. Uncontrolled intercurrent illness that in the opinion of the investigator would limit compliance and tolerance to study requirements 5. Patients with known brain metastases or leptomeningeal tumor involvement. 6. Receiving any of the following: concomitant antitumor therapy or inhibitors of CYP3A4. 7. Patients with history of interstitial lung disease and/or pneumonitis.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determine the maximum tolerated dose (MTD) and dose limiting toxicities (DLTs) of ABI-009 administered weekly and pharmacokinetic parameters for ABI-009. | End of Study (EOS) and Follow Up |
Secondary
| Measure | Time frame |
|---|---|
| Efficacy of ABI-009 in this patient population | End of Study (EOS) and Follow Up |
Countries
United States
Outcome results
None listed