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RECRUITINGPhase 2INTERVENTIONAL

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

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: 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. Who Should NOT Join This Trial: 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; Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
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;

Treatments Being Tested

DRUG

Liposomal Irinotecan and Apatinib

Liposomal Irinotecan in Combination With Apatinib

Locations (1)

Second Affiliated Hospital of Zhejiang University
Hangzhou, Zhejiang, China