Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Age > 20 years
Signed informed consent
Histologically documented, incurable, locally advanced or metastatic cancers that have failed to respond to at least one prior regimen or for which there is no standard therapy.
Disease that is measurable or evaluable by RECIST 1.1 criteria (for Solid Tumors)
ECOG performance status 0-2
Documented negative pregnancy test for women of childbearing potential and use of an effective means of contraception for both men and women while enrolled in the study
Granulocyte count ≥ 1,500/㎣, platelet count ≥ 100,000/㎣, and hemoglobin ≥ 9 g/dL
Serum bilirubin ≤ 1.5 x upper limit of normal (ULN)(≤ 3 x ULN if liver metastatic cancer)
Alkline phosphatase, AST and ALT ≤ 2.5 x ULN (≤ 5 x ULN if liver metastatic cancer)
Serum creatinine ≤ 1.5 mg/dL
INR (international normalized ratio) ≤ 1.3, and aPTT (activated partial thromboplastin time) ≤ 1.5 x ULN
Subject had to have a projected life expectancy of at least 3 months
Bazetts correction QTc < 450 msec in ECG at Screening

Exclusion Criteria:

Less than 4 weeks since last chemotherapy (including biologic unless previous Avastin treatment, experimental, and hormonal therapy), radiation therapy, or major surgical procedure
All incisions from any procedure must be fully healed and sutures removed prior to infusion on Day 1
Pleural effusions, ascites, or leptomeningeal disease as the only manifestation of the current malignancy
Subjects that have hypertension that is remained uncontrolled, despite drug regimen.
Subjects with grade III or IV hemorrhage/bleeding and who have experienced pulmonary hemorrhage/hemoptysis (exceed size of 2.5 mL of erythrocyte) or who have experienced grade III/IV hemorrhage/bleeding.
The presence of gastrointestinal perforation
The presence of tracheoesophageal fistula or grade Ⅳ fistula
Subjects with grade Ⅳ proteinuria (nephritic syndrome)
The presence of arterial thromboembolic events
Subjects who have history of life threatening (grade Ⅳ) pulmonary embolism
Subjects with a known hypersensitivity to CHO cell product or other recombined human or humanized antibody
Subjects with mental illness
Subjects with a known hypersensitivity to any of the ingredients/substrates in investigational product of this study
Subjects who given any investigational drug within longer period between 30 days and 5 times of half life before participation in this study
Active infection requiring IV antibiotics
Active autoimmune disease that is not controlled by drugs
Clinically important history of liver disease, including viral or other active hepatitis, current alcohol abuse, or cirrhosis
Known human immunodeficiency virus (HIV) infection
Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect the interpretation of the results or renders the subjects at high risk from treatment complications
Significant traumatic injury within 3 weeks of Day 1
Inability to comply with study and follow-up procedures