Status:
COMPLETED
An A/B Dose Escalation Study of AbGn-7 Alone and With FOLFOX7 Treatment in Patients With Advanced Solid Tumors
Lead Sponsor:
AbGenomics B.V Taiwan Branch
Conditions:
Solid Tumor of Epithelial Origin
Gastric Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
The purpose of this study is to determine the safety and tolerability profile including the dose limiting toxicity of AbGn-7 in patients with chemo-refractory advanced solid tumor of epithelial origin...
Detailed Description
Monoclonal antibodies, alone or in combination with chemotherapeutic agents, have been proven to be effective treatment for many malignant diseases in human. Antibodies can mediate cytotoxicity throug...
Eligibility Criteria
Inclusion
- must provide written informed consent.
- must be ≥18 years of age, either sex and of any race/ethnicity.
- Phase 1a: must have a histologically or cytologically confirmed advanced malignant solid tumor of epithelial origin and must have failed on previous chemotherapy. Phase 1b: must have a histologically or cytologically confirmed, recurrent, locally advanced or metastatic gastric cancer with measurable disease; must be chemo-naïve or must have failed on previous chemotherapy; must not have received an oxaliplatin-based chemotherapeutic regimen or monoclonal antibody therapy.
- must have an Eastern Cooperative Oncology Group Performance Status of ≤2.
- must have adequate hematological, renal and liver functions within 3 weeks prior to first study drug administration as evidenced by: a) Absolute neutrophil count ≥1.5 x 109/L, b) Hemoglobin ≥90 g/L (≥80 g/L for patients with documented renal cell carcinoma), c) Platelet count ≥100 x 109/L, d) Serum creatinine ≤1.5 x upper limit of normal ULN or a calculated creatinine clearance ≥60 mL/minute, e) Total bilirubin \<1.5 x ULN, except for patients with documented Gilbert's disease, f) AST/SGOT and ALT/SGPT \< 2.5 x ULN, or, in the presence of documented liver metastases, ≤5 x ULN.
- must be able to adhere to dose and visit schedules.
- Each female patient of childbearing potential must agree to use a medically accepted method of contraception or to abstain from sexual intercourse and each male patient must agree to use a medically accepted method of contraception or to abstain from sexual intercourse during the study and for 60 days after stopping the study drug.
- A life expectancy of at least 3 months.
- Available tumor tissue in the form of unstained slides for determination of AbGn-7 epitope expression (optional for Phase 1a, obligatory for Phase 1b). Patients without archival/banked tumor tissue obtained at the time of initial diagnosis must have a biopsy performed according to institutional guidelines prior to the initiation of treatment.
Exclusion
- No current treated or untreated leptomeningeal metastasis or a metastatic CNS lesion.
- For Phase 1a, patients should not have received chemotherapy within 30 days prior to initiation of AbGn-7 therapy. For Phase 1b, patients should not have received oxaliplatin-based chemotherapy or monoclonal antibody therapy for their gastric cancer prior to enrollment.
- Have note received radiation therapy within 3 weeks prior to first study drug administration and must have adequately recovered from any associated toxicity and/or complications of this intervention.
- Have not undergone major surgery within 3 weeks prior to the first study drug administration and must have adequately recovered from the toxicity and/or complications of these interventions.
- No current human immunodeficiency virus (HIV) infection or a current HIV-related malignancy.
- No current active hepatitis B or C.
- No any serious or uncontrolled infection.
- No uncontrolled diabetes mellitus, defined as a HbA1c of ≥7.5% in a patient with documented diabetes mellitus.
- No any of the following within 6 months prior to first study drug administration: myocardial infarction, severe/unstable angina pectoris, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, clinically significant cardiac dysrhythmia or clinically significant ECG abnormality, cerebrovascular accident or transient ischemic attack, or seizure disorder.
- No persistent, unresolved NCI CTCAE Grade ≥2 drug-related toxicity associated with previous chemotherapy.
- Not participating in any other clinical study with a potentially therapeutic agent, or have not received another investigational product within 21 days.
- No any clinically significant condition or situation which would interfere with the study evaluations or optimal participation in the study.
Key Trial Info
Start Date :
November 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2013
Estimated Enrollment :
13 Patients enrolled
Trial Details
Trial ID
NCT01466569
Start Date
November 1 2011
End Date
January 1 2013
Last Update
June 23 2015
Active Locations (4)
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1
Fox Chase Cancer Center
Rockledge, Pennsylvania, United States, 19046
2
The University of Texas Health Science Center-CTRC
San Antonio, Texas, United States, 78229
3
MacKay Memorial Hospital
Taipei, Taiwan, 104
4
National Taiwan University Hospital
Taipei, Taiwan, 104