A Phase I Study of Anlotinib on Tolerance and Pharmacokinetics

The primary objective of this trial is to explore the maximum tolerated dose(MTD), dose-limiting toxicity(DLT) of ALTN and rational dosage regimen for phase II study, to investigate the pharmacokinetics with single and multiple doses of ALTN from 5mg/d,10mg/d,16mg/d,12mg.

Inclusion criteria

• late malignant tumor patients diagnosed with the pathological and/or cytological;
• lack of the standard treatment or treatment failure;
• 18-65years, ECOG:0-1,Expected survival period >3 months;
• stop medicine > 30 days if any other chemotherapy drugs be used.
• HB≥90g/L,ANC(Absolute Neutrophil Count) ≥1.5×109/L；PLT ≥100×109/L ,BIL/ALT/AST(aspartate aminotransferase )/Cr in normal range,or CCR≥60ml/min,TG≤ 3.0mmol/L，cholesterol≤7.75mmol/L; LVEF≥LLN.
• Female should be agreed to use contraceptive during the study and after 6 months (such as intrauterine device(IUD), the pill or a condom); The serum or urine pregnancy test negative before take ALTN, and is out of non-lactation period. Male should be agreed to use contraceptive during the study and after the period of 6 months.
• Volunteer, informed consent form (ICF) signed, compliance.

Exclusion criteria

• Subject was diagnosed with other malignant tumors previously or meanwhile;
• Participated in other clinical trials in four weeks;
• Has influence of oral drugs(such as unable to swallow, gastrointestinal tract after resection);
• Already diagnosed with brain metastases, spinal cord compression, cancerous meningitis, or screening CT or MRI findings of the brain or soft meningeal disease patient;
• Hypertension
• Urine protein: ++, and urinary in 24 hours > 1.0g;
• Coagulant function abnormality: subject with bleeding tendency (such as active peptic ulcer) or are receiving thrombolysis or anticoagulant therapy;
• Subject with psychiatric drugs abuse history and can't get rid of, or mental disorder;
• With artery/venous thrombotic before oral ALTN;
• With history of anticoagulant, vitamin K antagonists(such as warfarin or heparin) or other analogues treatment;
• With Abnormal thyroid function;
• With history of psychiatric drugs abuse or a mental disorder;
• Viral hepatitis B or hepatitis c patients (including hepatitis b, hepatitis c virus carriers);
• Have immunodeficiency history;
• According to the researcher's judgment,there are concomitant diseases which will seriously endanger the patients or obstruct the patients to complete the clinical trial.