Safety, Pharmacokinetic and Preliminary Efficacy Study of AC0010 in Patients With EGFR T790M Positive NSCLC

Exclusion Criteria

• •1. No pathology confirmation.
• •2. HCV positive, active hepatitis B.
• •3. History of interstitial lung disease related to prior EGFR inhibitor therapy.
• •4. Positive to HIV antibody or other immunodeficiency disease or organ transplantation.
• •5. Residue toxicity related to prior therapies \> grade 1.
• •6. BUN or Cr \> 1.5 × upper limits of normal.
• •7. ALT or AST \> 2.5 × upper limits of normal, total bilirubin\> 1.5 × upper limits of normal.
• •8. Fever (temperature\>38℃ or any uncontrolled active infections.
• •9. Patients received high-dose glucocorticoid or any other immunosuppression within 1 month.
• •10. Any severe or uncontrolled disease, such as mental, neurologic, cardiovascular, respiratory diseases.
• •11. Patients with symptomatic and untreated brain metastasis.
• •12. Patients with organic heart disease, cardiac insufficiency, \>2 degree heart block, experienced myocardial infarction in 6 months. Abnormal PR, QT, QRS interval (defined as: 12 lead electrocardiogram QT interval correlated to Bazetts (QTcB)\>450ms (male) or \>470ms (female), PR\>240ms, QRS\>110ms).
• •13. Patients receiving medication known to prolong QT interval.
• •14. Past history of major surgery in 14 days prior to enrollment.
• •15. Pregnant or lactating women.
• •16. Any other reasons for the investigator to consider the patient should not participate in the study.
• •1. Acute and chronic hepatitis C, active hepatitis B (including positive HBsAg and/or HBeAg; HBcAb and/or positive HBeAb and positive HBV DNA), hepatitis E Virus IgM antibody positive.
• •2. History of interstitial lung disease related to prior EGFR inhibitor therapy.
• •3. Positive to HIV antibody or other immunodeficiency disease or organ transplantation.
• •4. Fever (temperature\>38℃ or any uncontrolled active infections.
• •5. Patients received high-dose glucocorticoid or any other immunosuppression within 1 month.
• •6. Any severe or uncontrolled disease, such as mental, neurologic, cardiovascular, respiratory diseases.
• •7. ECG showed abnormal rhythm, conduction and form, such as complete left bundle branch block, \>2 degree heart block, PR interval \>250ms, experienced myocardial infarction in 6 months. Risks leading to prolonged QT interval or arrhythmia, such as heart failure, hypokalemia, congenital long QT, long QT family history or sudden death under 40 years old in first degree relatives (12 lead electrocardiogram QT interval correlated to Bazetts (QTcB) \> 450ms.
• •8. Prior history of malignancies other than NSCLC (except cured malignancy such as removed basal-cell carcinoma and carcinoma in situ) within 5 years.
• •9. Patients with CNS metastasis (except asymptomatic CNS metastasis with stable radiography in 4 weeks and no long-term use of corticosteroid. CNS metastasis focuses ≤2, maximum diameter of focus \<10mm)
• •10. Radiation field covered more than 30% bone marrow within 4 weeks of enrollment.
• •11. Lab test of 1ml plasma prove treatment of AZD9291.
• •12. Patients already received treatment of this research or quite the treatment of this research. Patients treated with 3rd generation of EGFR-TKI (AZD9291, AC0010, BPI-15086, CO-1686, HM61713).
• •13. Past history of major surgery in 14 days prior to enrollment.
• •14. Pregnant or lactating women.
• •15. Patients with uncontrolled pleural effusion and/or pericardial effusion.
• •16. Any other reasons for the investigator to consider the patient should not participate in the study