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

NCT03308201 | Completed Phase 1

• 1 other identifier: HM022BC1C01
• Study Type: interventional
• Target: 55
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to evaluate the safety and tolerability of Hemay022 combined with endocrine therapy in the treatment of ER and HER2-positive metastatic or advanced breast cancer, and to establish OTR (best tolerated regimen). The second purpose of this study is to evaluate the pharmacokinetics and efficacy of Hemay022 in combination with exemestane, and the safety of Hemay022 in combination with letrozole or fulvestrant. The research will be divided into two parts. In the first part, 15 to 24 subjects will be enrolled to determine the safety and tolerability of combining Hemay022 with exemestane in patients with HER2-positive advanced breast cancer. The second part will enroll about 24-36 other subjects with ER and HER2-positive advanced breast cancer to better determine the tolerability and preliminary efficacy of Hemay022.

Conditions

Breast Cancer

Outcome Measures

Primary Outcomes (1)

• Number of participants with adverse events

  from baseline until 4 weeks after the study day

Secondary Outcomes (7)

• Objective response rate (complete response rate + partial response rate) according to RECIST v1.1

  At screening, every 8 weeks of treatment up to 18 months

• Clinical benefit rate defined as percentage of patients with stable disease (SD) ≥ 6 months/partial response (PR)/complete response (CR). according to RECIST v1.1

  At screening, every 8 weeks of treatment up to 18 months

• Progression Free Survival defined as the proportion of patients alive and without progression (according to RECIST v1.1 criteria)

  18 months after treatment initiation

• Observed maximum concentration of Hemay022 and exemestane

  0, 0.5, 1, 2, 3, 4, 8, 12, 24 hours post-dose on day 1 and day 28

• Time of maximum concentration of Hemay022 and exemestane

  0, 0.5, 1, 2, 3, 4, 8, 12, 24 hours post-dose on day 1 and day 28

Study Arms (3)

Hemay022 and Exemestane

EXPERIMENTAL

Part one: Hemay022 in combination with exemestane will be taken orally once daily. Planned dose escalation of Hemay022 will be 200mg, 300mg,400mg or 500mg daily for 28 days. Part two: Hemay022 in combination with exemestane will be taken in OTR dose until disease progression, intolerable toxicity or death.

Drug: Hemay022+exemestane

Hemay022 and Letrozole

EXPERIMENTAL

Part two: Hemay022 in combination with letrozole will be taken in OTR dose until disease progression, intolerable toxicity or death.

Drug: Hemay022+letrozole

Hemay022 and Fulvestrant

EXPERIMENTAL

Part two: Hemay022 in combination with fulvestrant will be taken in OTR dose until disease progression, intolerable toxicity or death.

Drug: Hemay022+ fulvestrant

Interventions

Hemay022+exemestane DRUG

Part one: Hemay022 tablets will be taken orally once daily in doses of 200mg, 300mg,400mg or 500mg for 28 days in combination with exemestane. Part two: Hemay022 tablets combination with exemestane.

Hemay022 and Exemestane

Hemay022+letrozole DRUG

Part two: Hemay022 combination with letrozole.

Hemay022 and Letrozole

Hemay022+ fulvestrant DRUG

Part two: Hemay022 combination with fulvestrant.

Hemay022 and Fulvestrant

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Breast cancer subjects diagnosed by tumor histology;
• Objective evidence shows that patients with metastasis or relapse who cannot be cured by standard treatment;
• ER positive (≥1%) and HER2 over-expression (immunohistochemical IHC test 3+ and/or in situ hybridization ISH test positive), Post-menopausal female subjects who are suitable for exemestane as endocrine therapy ; Remarks: The expansion period is planned to include 6 subjects combined with letrozole and 6 subjects combined with fulvestrant in the 400mg dose group. Therefore, for this part of the subjects, the expansion period is included " Post-menopausal female subjects who are suitable for letrozole or fulvestrant as endocrine therapy";
• 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); Remarks: 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 zoladex ovarian suppression therapy. Ovarian suppression therapy has been started at least 14 days before the start of this program, and Must be continued during the treatment plan; For subjects whose postmenopausal status is difficult to judge, the investigator and medical personnel of the sponsor will determine whether to enter the group after discussion.
• At least one evaluable tumor lesion (according to RECIST1.1) or only bone metastases;
• ECOG Performance Status of 0-1;
• The estimated survival time is more than 3 months;
• Bone marrow function meets: ANC≥1.5×109/L, HB≥90 g/L (allowed for blood transfusion), PLT≥80×109/L. Liver function satisfies: ALT≤2.5×ULN, AST≤2.5×ULN, TBIL≤1.5×ULN (ALT≤5×ULN, AST≤5×ULN in patients with liver metastases); renal function satisfies: blood creatinine ≤1.5×ULN;
• Subjects must give informed consent to the study before the study entry and voluntarily sign a written informed consent form;
• The subject can communicate well with the investigator and can complete the research in accordance with the research regulations.

You may not qualify if:

• There are life-threatening visceral metastases, any central nervous system metastases or leptomeninges carcinomatosis;
• 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.
• The first-line endocrine therapy was used in the late stage, and the drug was stopped for less than 4 weeks;
• Have received radiotherapy within 4 weeks prior to study;
• 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);
• Patients with parenteral nutrition; malabsorption syndrome; or any condition possibly affecting drug absorption or inability to tolerate oral medications;
• 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;
• 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);
• Left ventricular ejection fraction (LVEF) \<50％ as measured by echocardiogram or MUGA scan;
• Positive blood for human immunodeficiency virus (HIV antibody), hepatitis B virus surface antigen, or hepatitis C virus antibody at screening;
• Complicated with ≥2 grade diarrhea or ≥2 grade nausea condition;
• Active infection (ie, requiring intravenous antibiotic or antiviral agent);
• Uncontrolled hypertension (systolic blood pressure\> 150 mmHg, diastolic blood pressure\> 100 mmHg after antihypertensive treatment);
• 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;
• 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);

Sponsors & Collaborators

• Tianjin Hemay Pharmaceutical Co., Ltd: lead

Study Sites (1)

Beijing Cancer Hospital

Beijing, China

Location

MeSH Terms

Conditions

Breast Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Breast Diseases; Skin Diseases; Skin and Connective Tissue Diseases

Study Officials

• Huiping Li

  Peking University Cancer Hospital & Institute

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 29, 2017
• First Posted: October 12, 2017
• Study Start: October 16, 2017
• Primary Completion: June 30, 2022
• Study Completion: March 1, 2023
• Last Updated: March 6, 2024

Record last verified: 2024-03

Locations

CN (1)