A Clinical Study of TQB2930 Injection and Chemotherapy With or Without Bevacizumab in the Treatme… (NCT07653685) | Clinical Trial Compass
Not Yet RecruitingPhase 1/2
A Clinical Study of TQB2930 Injection and Chemotherapy With or Without Bevacizumab in the Treatment of Advanced Colorectal Cancer
China71 participantsStarted 2026-07
Plain-language summary
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).
Who can participate
Age range
18 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 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
Exclusion Criteria:
* 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 …
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Recommended Phase 2 Dose
Timeframe: Baseline up to 21 days
2
Adverse event (AE)
Timeframe: From the subject's signing of the informed consent form to 28 days after the last dose or the start of new anti-tumor therapy (whichever occurs first)
3
Objective Response Rate
Timeframe: Baseline up to 24 months
Trial details
NCT IDNCT07653685
SponsorChia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.