About this trial
This study will evaluate the efficacy and safety of irinotecan liposome(II) in combination with Ivonescimab as second line treatment for SCLC.
Eligibility criteria
Qualifiers
Age ≥18 years;
Histologically or cytologically confirmed SCLC;
Advanced SCLC who failed first-line platinum-based chemotherapy with or without checkpoint inhibitors;
The Eastern Cancer Cooperative Group (ECOG) performance score of 0 or 1;
Disqualifiers
Known allergy to irinotecan hydrochloride liposome injection (II) and eboxizumab or drug excipients
History of severe active autoimmune disease
Participated in other drug studies within 4 weeks before enrollment
Imaging during the screening period showed that the tumor surrounded important blood vessels or had significant necrosis and voids, and the investigators determined that entering the study would cause bleeding risk
Trial design
Treatments tested in this trial
- irinotecan liposome(II) plus Ivonescimab via intravenously (IV) Q3W for 4-6 cycles, followed by Ivonescimab until disease progression or intolerable toxicity
Treatment groups
Sponsors and collaborators
The Second Affiliated Hospital of Dalian Medical University
Lead sponsor
Shengjing Hospital
Collaborator