Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:53 AM
Ignite Modification Date:
2025-12-25 @ 12:53 AM
NCT ID:
NCT02330367
Eligibility Criteria:
Inclusion Criteria - phase 1:
1. Patients of either gender, aged from 18 years older to 75.
2. Histologically or cytologically confirmed metastatic, or unresectable locally advanced, recurrent NSCLC.
3. At least one measurable disease by CT or MRI, according to RECIST Version 1.1.
4. Failed to the treatment of EGFRTKI with definite state of T790M, or harbored T790M mutation without the treatment of EGFRTKI.
5. Offer biopsy sample to central lab if failed or without the treatment of EGFRTKI.
6. Adequate hematological and physiological functions of heart, lung, liver, and kidney according to definitions given in Appendix D.
7. Any prior treatment (including chemotherapy, radiotherapy, biotherapy and other clinical medicine) must be completed over 28 days or 5 half-lives from the screening.
8. ECOG (Eastern Cooperative Oncology Group) performance status of 0 to 1.
9. NSCLC patients with asymptomatic brain metastasis or drug-controllable brain metastasis.
10. Life expectancy of at least 3 months.
11. Patients should cooperate with investigator to observe adverse events and efficacy.
12. Without other anticancer therapy.
13. Women without pregnancy or breastfeeding.
14. Adequate function of blood coagulation (INR≤1.5)
15. Signed consent on an Independent Ethics Committee-approved Informed Consent Form prior to any study-specific evaluation.
Exclusion Criteria - Phase 1:
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.
Inclusion Criteria - Phase 2:
1. Patients of either gender, aged from 18 years older to 75.
2. Histologically or cytologically confirmed metastatic, or unresectable locally advanced, recurrent NSCLC.
3. At least one measurable disease by CT or MRI, according to RECIST Version 1.1.
4. Failed to the treatment of EGFR-TKI and harbored T790M mutation.
5. Offer biopsy sample to central lab if failed or without the treatment of EGFRTKI.
6. Patients failed the treatment of EGFR-TKI should be treated with only one kind of medicine. Patients with arbored T790M mutation should be treated with only one kind of medicine or never be treated.
7. Comply with the results of laboratory testing.
8. ECOG (Eastern Cooperative Oncology Group) performance status of 0 to 1 and no deterioration in 2 weeks.
9. Life expectancy of more than 12 weeks.
10. Patients should cooperate with investigator to observe adverse events and efficacy.
11. Women without pregnancy.
12. Signed consent on an Independent Ethics Committee-approved Informed Consent Form prior to any study-specific evaluation.
Exclusion Criteria - Phase 2:
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
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT02330367
Study Brief:
Protocol Section:
NCT02330367