Ivonescimab Plus Chemotherapy in Patients With Initially Unresectable Colorectal Cancer Liver Metastases

NCT ID: NCT06848842

Last Updated: 2025-10-01

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-09-18
• Study Completion Date: 2027-06-30

Brief Summary

The goal of this clinical trial is to learn if ivonescimab plus chemotherapy works to treat colorectal cancer liver metastases that cannot be completely removed. It will also learn about the safety of ivonescimab. The main questions it aims to answer are:

Does ivonescimab plus chemotherapy raise the objective response rate? What medical problems do participants have when receiving ivonescimab plus chemotherapy?

Participants will:

Receive ivonescimab and chemotherapy every 3 weeks, no more than 8 cycles. Visit the clinic once every 2 cycles (6 weeks) for checkups and tests. Receive curative surgery, maintenance therapy, or discontinue study treatment according to the expert team's evaluation.

Conditions

Colorectal Liver Metastases

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Experimental group

Ivonescimab plus chemotherapy

Group Type: EXPERIMENTAL

Ivonescimab plus chemotherapy

Intervention Type: DRUG

Ivonescimab, 20mg/kg, D1, Q3W; Oxaliplatin, 130mg/m2, D1, Q3W; Capecitabine, 1000mg/m2, BID, D1-D14, Q3W

Interventions

Ivonescimab plus chemotherapy

Ivonescimab, 20mg/kg, D1, Q3W; Oxaliplatin, 130mg/m2, D1, Q3W; Capecitabine, 1000mg/m2, BID, D1-D14, Q3W

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age ≥18 years.

2. Histologically confirmed colorectal adenocarcinoma.

3. Radiologically confirmed liver-only metastases. Patients with ≤1 cm extrahepatic lesions not confirmed as metastatic are eligible.

4. No prior systemic therapy or local therapy for metastatic lesions, or completion of neoadjuvant/adjuvant chemotherapy ≥6 months before diagnosed disease recurrence.

5. Liver metastases considered unresectable or borderline resectable by multidisciplinary evaluation.

6. Liver metastases were measurable according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.

7. Eastern Cooperative Oncology Group performance status 0-1

8. Life expectancy ≥12 weeks.

9. No contraindications to hepatic resection/ablation, and primary tumor resectable or previously resected.

10. Adequate organ function as determined by normal bone marrow function (hemoglobin ≥80 g/L, absolute neutrophil count ≥1.5×10⁹/L, and platelets ≥100×10⁹/L), renal function (serum creatinine ≤1.5×upper limit of normal [ULN] and creatinine clearance ≥30 mL/min), liver function (serum bilirubin ≤2×ULN and serum transaminases ≤5×ULN).

Exclusion Criteria

1. Definite extrahepatic metastases.

2. dMMR or MSI-H colorectal cancer.

3. Intolerance to the study drug during prior neoadjuvant/adjuvant therapy.

4. Toxicities from prior therapy have not resolved to ≤ Grade 1 (according to NCI-CTCAE v5.0), except for alopecia (any grade) and peripheral neuropathy (≤ Grade 2).

5. History of or concurrent other malignancies within the past 5 years, except cured localized tumors.

6. Surgery performed within 28 days prior to enrollment.

7. Hypertension with systolic blood pressure ≥160mmHg or diastolic blood pressure ≥100mmHg despite antihypertensive treatment.

8. Major cardiovascular events within 12 months prior to enrollment.

9. History of severe bleeding tendency or coagulation disorders; tumor encasement of major blood vessels or significant necrosis or cavitation, and the investigator deems participation in the study may pose a bleeding risk.

10. Active autoimmune disease requiring systemic treatment within the past 2 years.

11. History of immunodeficiency, positive HIV antibody test, or long-term use of corticosteroids or other immunosuppressants.

12. Prior history of allogeneic bone marrow or organ transplantation.

13. Received live vaccines within 30 days prior to the first dose or plans to receive live vaccines during the study period.

14. Allergy to any component of the study drugs; history of severe hypersensitivity reactions to other monoclonal antibodies.

15. Women who are pregnant or breastfeeding.

16. Severe comorbidities or any other condition that precludes safe administration of the study treatment, including but not limited to symptomatic congestive heart failure (Class II or higher per NYHA classification), unstable angina, acute myocardial ischemia, poorly controlled arrhythmias, decompensated cirrhosis, nephrotic syndrome, uncontrolled metabolic disorders, severe active peptic ulcer disease or gastritis, or psychiatric/social conditions that may limit compliance with study requirements or impair the subject's ability to provide written informed consent.

17. Any other condition deemed by the investigator as unsuitable for participation in this study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

OTHER

Sponsor Role: lead

Responsible Party

LIN YANG

Prof

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

Beijing, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Lin Yang

Role: CONTACT

linyangcicams@126.com

8613681015148

Facility Contacts

Lin Yang

Role: primary

linyangcicams@126.com

8613681015148

Other Identifiers

NCC5043

Identifier Type: -

Identifier Source: org_study_id