ARX788 in Breast Cancer With Low Expression of HER2

• Status: Not yet recruiting
• Trial end date: 2023-06-30
• Target enrollment: 0
• Participant gender: All

Summary

A Phase 2 Study of ARX788 in unresectable and/or metastatic breast cancer with low expression of HER2.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Fudan University

Criteria

Inclusion Criteria:

• Willing and able to understand and sign an informed consent inform;

• Age ≥18 years, and ≤75 years, male or female;

• Diagnosed as HR arbitrary/HER2 low expression unresectable and/or metastatic breast cancer. HER2 low expression is defined as HER2 IHC 1+ (FISH negative or FISH not done) or HER2 IHC 2+ and FISH negative;

• Received ≥2 lines of systemic chemotherapy regimens for recurrent or metastatic disease, and for HR positive subjects, also need to have received ≥2-line endocrine therapy ± targeted therapy (including neoadjuvant/adjuvant therapy);

• Never had a HER2 positive result (IHC 3+ or FISH+) in previous pathological examinations;

• Have archived or fresh tumor tissue samples for HER2 status confirmation;

• According to the RECIST 1.1 standard, there is at least one measurable lesion;

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or1; LVEF≥50%;

• Adequate organ functions;

• Acute toxicities from any prior therapy, surgery, or radiotherapy must have resolved to Grade ≤1;

• Life expectancy ≥ 3 months.

Exclusion Criteria:

• History of allergic reactions to any component of ARX788, or with a history of protein drug allergy, a history of specific allergies (asthma, rheumatism, eczematous dermatitis), or a history of other severe allergic reactions, who are unsuitable for ARX788 treatment as per the investigator's judgments;

• Previous treatment with T-DM1 or other HER2-ADC drugs;

• Have other malignant tumors within 5 years before signing the informed consent form (except for non-melanoma skin cancer, cervical carcinoma in situ or other tumors that have been effectively treated, except malignant tumors that are considered cured);

• Have primary central nervous system (CNS) tumors or CNS metastases;

• Prior history of interstitial pulmonary disease requiring hormone therapy, drug-induced interstitial pulmonary disease, radiation pneumonia, or current clinically active interstitial pulmonary disease;

• Suffering from keratitis, corneal diseases, retinal diseases or active eye infections that require intervention;

• Unwilling or unable to stop wearing contact lenses for the duration of the study;

• Cardiac insufficiency;

• Uncontrolled hypertension;

• Suffering severe or uncontrolled systemic diseases;

• Had chemotherapy, radiotherapy, or immunotherapy within 4 weeks before the first dose;

• Had breast cancer endocrine therapy within 2 weeks before the first dose;

• Had palliative radiotherapy for bone metastasis within 2 weeks before the first dose;

• Any uncontrolled infection, or other conditions that may limit trial compliance or interfere with evaluation;

• Current known active infection with human immunodeficiency virus (HIV), hepatitis B virus, hepatitis C virus or syphilis;

• Plan to receive major surgical treatment within 2 weeks before first dose or during the trial period, or have suffered severe traumatic injury;

• Pregnancy or lactation;

• Unwilling or unable to use acceptable methods for contraception during the entire treatment period of this trial and within 8 months after the last dose;

• Participated in other clinical trials and used other experimental drugs within 4 weeks before the first dose;

• Any mental or cognitive impairment may limit their understanding and implementation of the informed consent form;

• Not suitable for participating in this trial, such as poor compliance.