NCT07653685尚未招募1 期
A Phase Ib/II Clinical Study to Evaluate the Efficacy and Safety of TQB2930 Injection and Chemotherapy With or Without Bevacizumab in Subjects With Human Epidermal Growth Factor Receptor 2 (HER2) Positive Unresectable Locally Advanced or Metastatic Colorectal Cancer
Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.24 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2026年7月1日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 71
- 试验地点
- 24
研究概览
简要总结
To assess the safety and preliminary efficacy of TQB2930 and chemotherapy with or without bevacizumab in subjects with HER2-positive unresectable locally advanced or metastatic colorectal cancer (CRC).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects voluntarily participate in this study, sign the informed consent form, and have good compliance
- •Age: 18-75 years (including the boundary when signing the informed consent form)
- •Eastern Cooperative Oncology Group (ECOG) score: 0-1
- •Expected survival of more than 3 months
- •Unresectable locally advanced or metastatic colorectal cancer diagnosed by histopathology/cytology
- •HER2 positive tested
- •Presence of at least one measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria
- •Subjects should agree to use contraception during the study and for 6 months after the end
排除标准
- •Patients with previously confirmed Microsatellite Instability Microsatellite Instability-High Deficient Mismatch Repair (MSI-H/dMMR)
- •Presence of conditions affecting intravenous, venous blood sampling, or multiple factors affecting oral medications
- •Active inflammatory bowel disease within 28 days prior to first dose
- •Other malignancies within 5 years prior to the first dose or currently suffering from other malignancies
- •Unresolved toxicity greater than CTCAE Grade 1 due to any prior therapy
- •Major surgical treatment, significant traumatic injury within 28 days prior to the first dose or anticipation of major surgery during study treatment
- •Had wounds or fractures that had not been healed for a long time
- •Cerebrovascular accident, deep venous thrombosis and pulmonary embolism within 6 months prior to the first dose
- •Patients with a history of psychotropic substance abuse who cannot quit or have mental disorders
- •Subjects with any severe and/or uncontrolled disease
- •Known tumor-related carcinomatous meningitis with symptoms of brain metastases or symptom control for less than 4 weeks
- •Patients with imaging suggestive of tumor invasion of major blood vessels or fatal massive hemorrhage due to tumor rupture or invasion of major blood vessels judged by the investigator to be very likely to occur during the study
- •Failure to control serous effusions requiring repeated drainage
- •Local radiotherapy or
- •Bone marrow irradiation > 30% for bone metastasis before the first medication
- •Known tumor-related spinal cord compression, weight-bearing bone pathological fracture, extensive bone metastasis, or uncontrollable tumor bone metastasis-related pain
- •Patients who have received chemotherapy, targeted therapy, immunotherapy or other systemic anti-tumor drug therapy before the first medication;
- •Received Chinese patent medicine treatment with anti-tumor indications in the package insert of National Medical Products Administration (NMPA) approved drugs before study treatment
- •History of live attenuated vaccination before the first dose or planned live attenuated vaccination during the study;
- •Previous history of severe allergy of unknown origin
- •According to the investigator's judgment, there are concomitant diseases that seriously endanger the subject's safety or affect the completion of the study, or the subject is considered unsuitable for other reasons
研究者
研究点 (24)
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