A Phase Ⅲ Study of Hemay022 in Combination With AI In Advanced Breast Cancer

Breast Cancer Clinical Trial

Official title:

A Phase Ⅲ Randomized, Open Label, Parallel, Multicenter To Assess Efficacy and Safety Study of Hemay022 in Combination With AI In Postmenopausal HER2+/ER+ Advanced Breast Cancer Patients Treated With Trastuzumab-containing Regimens

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06313983
• Other study ID #: HM022BC3C01
• Status: Recruiting
• Phase: Phase 3
• Start date: January 8, 2022
• Est. completion date: June 2026

Study information

• Verified date: March 2024
• Source: Ganzhou Hemay Pharmaceutical Co., Ltd
• Contact: Huiping Li
• Phone: 13811012595
• Email: huipingli2012[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of Hemay022 combined with AI (exemestane or letrozole) in the treatment of ER+/HER2+ advanced breast cancer patients based on the progression-free survival (PFS) assessed by the independent review committee (IRC). The second purpose of this study is to evaluate the pharmacokinetics and efficacy of Hemay022 in combination with AI, and the safety of Hemay022 in combination with AI. The trial plans to recruit 339 subjects, who will be randomly divided into two cohorts (the experimental group is hemay022 combined with AI, and the control group is lapatinib combined with capecitabine). During the treatment period, imaging examinations and anti-tumor efficacy evaluations will be performed regularly until the subject develop disease progression or starts receiving other treatments or dies or refuses to come to the hospital for follow-up or the trial is terminated, etc.

Other known NCT identifiers

• NCT05122494

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 339
• Est. completion date: June 2026
• Est. primary completion date: December 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Age =18 years old;

2. Subjects must give informed consent to the study before the study entry and voluntarily sign a written informed consent form;

3. Breast cancer subjects diagnosed by pathology(histology or cytology);

4. ER positive and HER2 over-expression (immunohistochemical IHC test 3+ and/or in situ hybridization ISH test positive);Previous test results are acceptable.

5. Advanced/metastatic breast cancer that has previously received treatment failure with trastuzumab (or trastuzumab biosimilar) regimen;Or (new) adjuvant therapy during treatment with trastuzumab (or trastuzumab biosimilar) or within 12 months after the end of treatment, disease recurrence or progression;Patients with first-line systemic treatment for relapse (previously received trastuzumab or trastuzumab biosimilars);Or patients who are not suitable for trastuzumab treatment;Patients who have failed previous anti-HER2-ADC drug therapy can also be included.

6. At least one lesion (measurable and/or non-measurable) that can be evaluated by CT/MRI and meets the reproducible evaluation requirements of RECIST V1.1;

7. ECOG Performance Status of 0-1;

8. The estimated survival time is more than 3 months;

9. Postmenopausal women Postmenopausal is defined as meeting any one of the following four conditions: Past bilateral oophorectomy; Age =60 years old; Age <60 years old, natural menopause =12 months, in the past 1 year without chemotherapy, tamoxifen, toremifene or ovarian castration, the level of follicle stimulating hormone (FSH) and estradiol Within the postmenopausal range (use the reference range of the local laboratory). Patients younger than 60 years old who are taking tamoxifen or toremifene, their FSH and estradiol levels are within the postmenopausal range (use the reference range of the local laboratory); Premenopausal or perimenopausal women who do not meet the above-mentioned menopausal criteria can also be included in this study, but they must also receive ovarian suppression therapy that meets the standards of medical or surgical castration treatment. Drug ovarian suppression therapy has been started at least 21 days before the start of this program, and Must be continued during the treatment plan;

10. Adequate bone marrow, liver, kidney, and coagulation Bone Marrow Function (No blood transfusion or adjuvant leukocyte or platelet augmentation drugs were used within 1 week before screening) Absolute value of neutrophils (ANC) =1.5×109/L Hemoglobin (HB) =90g/L (transfusion allowed) Platelet (PLT) =80×109/L Liver function Liver function grade Child-Pugh A/B (=9 points) Alanine transferase (ALT) or aspartate aminotransferase (AST) =2.5 ULN in the absence of liver metastasis; ALT or AST= 5x ULN with liver metastasis Renal function: serum creatinine =1.5 times ULN;

11. All previous treatment-related toxicities must be CTCAE (version 5.0) = Grade 2 at the time of randomization, except for hair loss, pigmentation, and long-term toxicity caused by radiotherapy (which cannot be recovered by the investigator's judgment);

12. Women patients of childbearing age (including their partners) have no pregnancy plan and voluntarily take effective contraceptive measures from the signing of the informed consent form to 3 months after the last medication.

Exclusion Criteria:

1. Patients with visceral crisis(Visceral crisis is defined as the dysfunction of several organs confirmed by symptoms, signs, laboratory tests, and rapid disease progression.Visceral crisis does not simply refer to the presence of visceral metastases, but to critical visceral conditions that require rapid and effective treatment to control the disease progression, especially when the opportunity for chemotherapy is lost after progression)

2. Patients with the presence of spinal cord compression or brain, meningeal metastases

3. Patients who have been treated with a small molecule HER2 tyrosine kinase inhibitor (HER2-TKI) (medication course =2 weeks is excluded)

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

5. Have received chemotherapy for advanced breast cancer> 1 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, lapatinib?AI (letrozole, exemestane) capecitabine or similar drugs.

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

10. Positive blood for human immunodeficiency virus (HIV antibody); Positive hepatitis B surface antigen and HBV-DNA>upper limit of normal; Active hepatitis C virus (HCV) infection

11. Patients with active infection requiring intravenous anti-infective treatment

12. 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)

13. Confirmed QTc prolongation (=500ms) (heart rate corrected according to Bazett formula or Fridericia formula)

14. People with a history of interstitial lung disease that needs treatment, a history of radiation pneumonitis, or clinically active interstitial lung disease

15. Have received other clinical trial drugs within 4 weeks before the study

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

17. The study period must be accompanied by other antitumor therapy,such as chemotherapy, targeted therapy, hormone therapy, immunotherapy, radiotherapy (except symptomatic local radiotherapy)

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

19. Any condition that would make the subject inappropriate for this study by the investigator's judgment

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• Hemay022+AI
hemay022:orally once daily,A 21-day cycle
• Lapatinib+Capecitabine
Take the pills according to the instructions

Locations

Country	Name	City	State
China	Beijing Cancer Hospital	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Tianjin Hemay Pharmaceutical Co., Ltd

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Median progression-free survival(mPFS)based on IRC assessment according to RECIST v1.1	PFS defined as the proportion of patients alive and without progression	From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Secondary	Overall Survival (OS) of the two group according to RECIST v1.1	OS is defined as the time from random to any cause of death	From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Secondary	Objective response rate ( ORR, partial response rate+ complete response rate) according to RECIST v1.1	ORR defined as the proportion of subjects in complete response (CR) or (partial response) PR	From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Secondary	Clinical benefit rate (CBR) according to RECIST v1.1	Clinical benefit rate defined as percentage of patients with stable disease (SD) = 6 months/partial response (PR)/complete response (CR).	From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Secondary	Duration of Response (DOR) according to RECIST v1.1	DOR defined as the duration after the first assessment as CR or PR, only applicable to subjects who have achieved remission	The earliest date from the first recorded CR or PR to the first recorded disease progression or death,assessed up to 100 months
Secondary	Time to Response (TTR)	TTR defined as the time from random to CR or PR for the first time	Start of treatment until the earliest date of CR or PR recorded for the first time,assessed up to 100 months