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A Study of SHR-A1811 Combined With Capecitabine in Treatment of Unresectable or Metastatic Breast Cancer With Low HER2 Expression.

Phase 1
Recruiting
Conditions
Breast Cancer
Interventions
Drug: SHR-A1811 for injection ; capecitabine
Registration Number
NCT05845138
Lead Sponsor
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Brief Summary

The study is being conducted to evaluate the safety, tolerability, preliminary efficacy, pharmacokinetics, and immunogenicity of SHR-A1811 combined with capecitabine in treatment of unresectable or metastatic breast cancer with low HER2 expression.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
116
Inclusion Criteria
  1. Women aged 18 to 75 (inclusive).
  2. HER2 low expression unresectable or metastatic breast cancer confirmed by histology or cytology.
  3. ECOG score is 0 or 1.
  4. An expected survival of ≥ 12 weeks.
  5. At least one measurable lesion according to RECIST v1.1 criteria.
  6. Women of childbearing potential (WOCBP) subjects must agree to use highly effective contraception for 7 months from the start of study screening until the last study medication and agree not to breastfeeding.
  7. Patients voluntarily joined the study and signed informed consent, had good compliance and willingness to cooperate with the visit and study related procedures.
Exclusion Criteria
  1. Have other malignancies within the past 5 years.
  2. Presence with uncontrollable third space effusion.
  3. Have surgical treatment, radiotherapy, chemotherapy, immunotherapy, molecular targeted therapy, biological therapy or other drug clinical studies within 4 weeks before the first medication.
  4. Accepted antibody drug conjugates containing etoisomercan derivative topoisomerase I inhibitor.
  5. Clinically significant cardiovascular disorders.
  6. Presence of active hepatitis B, hepatitis C, cirrhosis,or serious infected persons requiring antibiotic, antiviral or antifungal control.
  7. The toxicity from previous anti-tumor treatment has not recovered to ≤ grade I.
  8. Known to be allergic to any study drug or any of its excipients, or to humanized monoclonal antibody products.
  9. Failure to swallow, chronic diarrhea, intestinal obstruction, or presence of other factors affecting drug administration and absorption.
  10. Presence of other serious physical or mental diseases or laboratory abnormalities.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
SHR-A1811 combined with capecitabineSHR-A1811 for injection ; capecitabine-
Primary Outcome Measures
NameTimeMethod
DLT(Phase I (dose exploration phase) ) [ Time Frame: 21 days after the first administration of each subject ]21 days after the first administration of each subject ]
Incidence of AEs(Phase I (dose exploration phase) )from Day1 to 40 days after last dose
Incidence of SAEs(Phase I (dose exploration phase) )from Day1 to 40 days after last dose
Objective response rate(Phase II (efficacy expansion phase))One year after the last subject was enrolled in the group
Secondary Outcome Measures
NameTimeMethod
Duration of response(DoR )One year after the last subject was enrolled in the group
Progression Free Survival(PFS)One year after the last subject was enrolled in the group
Objective response rate(Phase I (dose exploration phase))One year after the last subject was enrolled in the group
Incidence of AEs(Phase II (efficacy expansion phase))from Day1 to 40 days after last dose
Incidence of SAEs(Phase II (efficacy expansion phase))from Day1 to 40 days after last dose

Trial Locations

Locations (9)

Wenzhou People's Hospital

🇨🇳

Wenzhou, Zhejiang, China

Cancer Hospital Chinese Academy of Medical Sciences

🇨🇳

Beijing, Beijng, China

Guangxi Medical University Affiliated Tumor Hospital & Oncology Medical College

🇨🇳

Nanning, Guangxi, China

The First Affiliated Hospital with Nanjing Medical University

🇨🇳

Nanjing, Jiangsu, China

Henan Provincial People's Hospital

🇨🇳

Zhengzhou, Henan, China

Shandong Cancer Hospital&Institute

🇨🇳

Jinan, Shandong, China

The Second Hospital of Anhui Medical University

🇨🇳

Hefei, Anhui, China

Shantou Central Hospital

🇨🇳

Shantou, Guangzhou, China

The First Hospital of China Medical University

🇨🇳

Shenyang, Liaoning, China

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