Study Evaluating Hemay022 in Combination With Endocrine Therapy In Subjects With ER Positive and HER2 Positive Advanced Breast Cancer

1. There are life-threatening visceral metastases, any central nervous system metastases or leptomeninges carcinomatosis;

2. Have received exemestane for breast cancer treatment (Note: If exemestane was previously used in the adjuvant treatment stage, and the drug has been stopped for ≥12 months before this enrollment, you can join the group); Remarks: For subjects who have been combined with letrozole in the extended phase, if they have received letrozole to treat breast cancer, they need to be excluded (if letrozole is used in the adjuvant treatment phase, and the drug has been stopped for ≥12 months before this enrollment , You can be included in the group); for subjects who have been combined with fulvestrant in the extended phase, if they have received fulvestrant for breast cancer, they need to be excluded.

3. The first-line endocrine therapy was used in the late stage, and the drug was stopped for less than 4 weeks;

4. Have received radiotherapy within 4 weeks prior to study;

5. Have received chemotherapy for advanced breast cancer\> 2 lines (the subjects who have used chemotherapy drugs must have stopped the chemotherapy drugs for ≥ 4 weeks before being enrolled in this study);

6. Patients with parenteral nutrition; malabsorption syndrome; or any condition possibly affecting drug absorption or inability to tolerate oral medications;

7. Use of any drug that inhibits or induces hepatic metabolism of Hemay022 within 2 weeks prior to study and entire study duration, for example CYP3A4 strong inhibitors or strong inducers;

8. Patients who are known to have a history of allergies to Hemay022, exemestane or similar drugs (Note: For patients who are planning to combine letrozole or fulvestrant, if they are known to be allergic to letrozole or fulvestrant History cannot be included in this study);

9. Left ventricular ejection fraction (LVEF) \<50％ as measured by echocardiogram or MUGA scan;

10. Positive blood for human immunodeficiency virus (HIV antibody), hepatitis B virus surface antigen, or hepatitis C virus antibody at screening;

11. Complicated with ≥2 grade diarrhea or ≥2 grade nausea condition;

12. Active infection (ie, requiring intravenous antibiotic or antiviral agent);

13. Uncontrolled hypertension (systolic blood pressure\> 150 mmHg, diastolic blood pressure\> 100 mmHg after antihypertensive treatment);

14. Significant heart diseases, including ischemic heart disease (NYHA III-IV), history of myocardial infarction or uncontrolled angina within 6 months, occurrence congestive heart failure within 3 months;

15. Arrhythmias requiring treatment , including atrial fibrillation, supraventricular tachycardia ,ventricular tachycardia, ventricular fibrillation, or patients with coronary heart disease have symptoms requiring medicine treatment, myocardial infarction within 1 year, congestive heart failure (CHF);

16. Confirmed ECG abnormalities, including QTc (heart rate corrected according to Bazett formula or Fridericia formula) prolongation (≥450msec), QRS\> 120ms;

17. History of hemorrhagic or thrombus events within 6 months, such as cerebrovascular accident (including transient ischemic attack), pulmonary embolism, spontaneous tumor bleeding;

18. Have received other clinical trial treatments or other targeted drugs within 4 weeks before the study;

19. Major surgery or injury less than 4 weeks before the study;

20. Other chemotherapy, targeted therapy, hormone therapy, immunotherapy, radiotherapy (except symptomatic local radiotherapy) during the research;

21. Any other malignant cancer within 5 years with the exception of adequately treated cervical cancer in situ or basal and squamous cutaneous cell carcinomas;

22. History of alcohol or drug abuse;

23. Serious psychogenic illness;

24. Evidence of significant medical illness or abnormal laboratory finding that would make the subject inappropriate for this study by the investigator's judgment;

25. Subjects could not complete the study due to other reasons.

What this study is about