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Trials / Not Yet Recruiting

Not Yet RecruitingNCT07095803

Ivonescimab (PD-1/VEGF Bispecific Antibody) Plus Radiofrequency Ablation for Multiple Advanced Tumors After PD-1 Therapy Failure

Ivonescimab (PD-1/VEGF Bispecific Antibody) Plus Radiofrequency Ablation for Multiple Advanced Tumors After PD-1 Therapy Failure: A Multicohort, Multicenter, Single-Arm Phase II Study

Status
Not Yet Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Sheng Zhang · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to learn if the combination of radiofrequency ablation (RFA) and Ivonescimab (PD-1/VEGF Bispecific Antibody) works to could reverse PD-1/PD-L1 resistance in patients with advanced tumors. It will also learn about the safety of this combination. The main questions it aims to answer are: Does the combination of RFA and Ivonescimab increase the objective response rate (ORR) of participants? What medical problems do participants have when taking the combination? Will the combination influence the progression-free survival time (PFS) and overall survival time and quality of life (QoL) of participants? Participants will: Patients received RGA treatment for less than three lesions. Patients were treated with Ivonescimab (20mg/kg Q3W, every 3 weeks) within 1 week before and after radiofrequency treatment until disease progression or intolerable toxicity occurred, or Ivonescimab was used for 2 years. Treatment effects will be evaluated every 9 weeks for 1 year and every 12 weeks thereafter.

Conditions

Interventions

TypeNameDescription
DRUGIvonescimab (20mg/kg Q3W)Patients received intravenous everciximab (20mg/kg Q3W) within 1 week before and after radiofrequency ablation.
PROCEDUREradiofrequency ablationPatients received radiofrequency treatment for less than three lesions.

Timeline

Start date
2025-08-01
Primary completion
2026-02-01
Completion
2027-02-01
First posted
2025-07-31
Last updated
2025-07-31

Source: ClinicalTrials.gov record NCT07095803. Inclusion in this directory is not an endorsement.