The primary goal of Phase Ib Study is to evaluate the safety of Suvemcitug in combination with trifluridine/tipiracil tablets in colorectal cancer participants.
The primary goal of Phase III Study is to evaluate the efficacy of Suvemcitug in combination with trifluridine/tipiracil tablets in colorectal cancer participants. Researchers will compare Suvemcitug + trifluridine/tipiracil tablets with placebo (a look-alike substance that contains no drug)+ trifluridine/tipiracil tablets to see if Suvemcitug + trifluridine/tipiracil tablets works better in treating refractory metastatic colorectal cancer.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* 1\. Confirmed by histological and/or cytological examination as unresectable metastatic colon or rectal adenocarcinoma;
* 2\. At least one measurable tumor lesion (RECIST v1.1);
* 3\. Previously received fluorouracil, oxaliplatin, and irinotecan based chemotherapy; had previously undergone or was unsuitable for anti-VEGF therapy. (For participants with RAS wild-type, had previously undergone or was unsuitable for anti-EGFR therapy.);
* 4\. Refractory metastatic colorectal cancer having progressed on or are intolerant to the last systemic treatment;
* 5\. Good organ and bone marrow function (no administration of hematopoietic growth factors, blood transfusion, or platelets within 14 days before screening hematology test);
* 6\. RAS mutation status confirmed by testing tumor tissue and /or blood sample.
Exclusion Criteria:
* 1\. Having a second active primary malignancy within the past 5 years;
* 2\. Symptomatic central nervous system (CNS) metastases or CNS metastases requiring local CNS-directed therapy (e.g., radiotherapy or surgery) or corticosteroid treatment within 2 weeks prior to the first administration of the study treatment;
* 3\. Any active infection requiring systemic treatment within 2 weeks prior to the initiation of the study treatment;
* 4\. Pleural effusion, pericardial effusion, or ascites that is uncontrolled or has required drainage or medical intervention within 4 weeks prior to the first administration of the study treatment;
* 5\. Received systemic immuno suppressive therapy within 4 weeks prior to randomization (excluding prophylactic use or chronic low-dose steroids \[≤20 mg/day prednisone equivalent dose\]);
* 6\. Currently taking or has recently taken (within 10 days prior to the first dose) aspirin (\>325 mg/day);
* 7\. Active or chronic hepatitis B (HBsAg or HBcAb positive and HBV DNA≥2000 IU/mL or ≥10000 copies/mL) or hepatitis C infection (HCV antibody positive and HCV RNA≥ULN);
* 8\. Clinically significant cardiovascular disease within 6 months prior to the first administration of the study treatment;symptomatic coronary artery disease requiring medication; arrhythmia requiring medication (excluding asymptomatic atrial fibrillation with controlled ventricular rate); QTcF interval \>470 ms at rest state; or uncontrolled hypertension or pulmonary hypertension;
* 9\. Known hereditary or acquired bleeding and thrombotic tendencies (e.g., hemophilia, coagulation disorders, thrombocytopenia, hypersplenism, etc.); clinically significant bleeding events, arterial or deep venous thrombotic events, or superficial venous thrombosis and intermuscular venous thrombosis requiring intervention within 6 months prior to enrollment;
* 10\. Participants with proteinuria (urine protein \>2+ found during screening examinations; or urine protein 2+ with 24-hour urine protein quantification ≥1g/24h);
* 11\. Participants with a history of intestinal obstruction (including incomplete intestinal obstruction) within 1 month prior to enrollment; participants with a history of abdominal fistula, gastrointestinal perforation, or abdominal abscess.
Primary outcome measure(s)
Phase Ib: dose limiting toxicity (DLT) — At the end of Cycle 1 (each cycle is 28 days)
Phase Ib: Adverse Events — From signing informed consent form until 28 days after the last dose of study treatment, up to about 18 months The incidence (number of participants) and severity of adverse events (AE) and serious adverse events (SAE) assessed by CTCAE v5.0
Phase Ib: Tolerance — From signing informed consent until 28 days after the last dose of study treatment, for up to 18 months Number of participants who experienced adverse event related dose interruption, dose reduction and treatment discontinuation as assessed by investigators.
Phase III: overall survival (OS) — For about 18 months from the randomization of the last participant OS is the time interval from the date of randomization to death from any cause.
Trial sites (6)
Facility
City
Region
Status
Fujian Cancer Hospital
Fuzhou
Fujian
Recruiting
Harbin Medical University University Cancer Hospital
Harbin
Heilongjiang
Recruiting
The First Affiliated Hospital of Nanjing Medical University
Nanjing
Jiangsu
Recruiting
Cancer Hospital of Shandong First Medical University
Jinan
Shandong
Recruiting
Tianjin Medical University Cancer Institute and Hospital
Tianjin
Tianjin Municipality
Recruiting
The Second Affiliated Hospital Zhejiang University School of Medicine
Hangzhou
Zhejiang
Recruiting
More Jiangsu Simcere Pharmaceutical Co., Ltd. trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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