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Clinical Trials in China / NCT06749691
Recruiting Phase 2

Liposomal Irinotecan and Apatinib in ES-SCLC

NCT06749691 · tracked via the Priya Life Science China tracker
Sponsor
Second Affiliated Hospital, Zhejiang University, School of Medicine
Phase
Phase 2
Started
2024-12-28
Last updated
2024-12-27

Condition(s) studied

Small Cell Lung Cancer Extensive Stage

Investigational drug(s) / intervention(s)

Liposomal Irinotecan and Apatinib

Liposomal Irinotecan and Apatinib: Liposomal Irinotecan in Combination With Apatinib

Study summary

The purpose of this study is to observe the efficacy and safety of liposomal irinotecan combined with apatinib in the treatment of extensive stage small cell lung cancer progressed from first-line regimen.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age range of 18-75 years; 2. Expected survival period ≥ 12 weeks; 3. At least one measurable lesion (according to RECIST V 1.1); 4. For patients who have failed first-line or second-line treatment. Exclusion Criteria: 1. Have received any systemic treatment targeting VEGF or VEGFR in the past, such as treatment with anti angiogenic drugs such as ranibizumab, fipronib, apatinib, anlotinib, lenvatinib, sunitinib, sorafenib. 2. Active or uncontrolled severe infection (CTCAE 5.0 ≥ 2) and/or antibiotic treatment within 2 weeks prior to enrollment; 3. There are multiple factors that affect the absorption of oral medication, such as inability to swallow, nausea and vomiting, chronic diarrhea, and intestinal obstruction; 4. Those deemed unsuitable for inclusion by doctors;

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Second Affiliated Hospital of Zhejiang University Hangzhou Zhejiang Recruiting

More Second Affiliated Hospital, Zhejiang University, School of Medicine trials in China

Other trials for the same condition

Official registry record

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.

View NCT06749691 on ClinicalTrials.gov ↗ ← All trials in China