RecruitingPhase 2NCT06749691

Liposomal Irinotecan and Apatinib in ES-SCLC

Study of Liposomal Irinotecan Combined with Apatinib in the Treatment of Extensive Stage Small Cell Lung Cancer After First-line Progression


Sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Enrollment

30 participants

Start Date

Dec 28, 2024

Study Type

INTERVENTIONAL

Conditions

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

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria4

  • Age range of 18-75 years;
  • Expected survival period ≥ 12 weeks;
  • At least one measurable lesion (according to RECIST V 1.1);
  • For patients who have failed first-line or second-line treatment.

Exclusion Criteria4

  • 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.
  • Active or uncontrolled severe infection (CTCAE 5.0 ≥ 2) and/or antibiotic treatment within 2 weeks prior to enrollment;
  • There are multiple factors that affect the absorption of oral medication, such as inability to swallow, nausea and vomiting, chronic diarrhea, and intestinal obstruction;
  • Those deemed unsuitable for inclusion by doctors;

Interventions

DRUGLiposomal Irinotecan and Apatinib

Liposomal Irinotecan in Combination With Apatinib


Locations(1)

Second Affiliated Hospital of Zhejiang University

Hangzhou, Zhejiang, China

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NCT06749691


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