Liposomal Irinotecan and Apatinib in ES-SCLC
Recruiting now · Phase 2
Conditions studied: Small Cell Lung Cancer Extensive Stage
In brief
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.
Key facts
- Study ID
- NCT06749691
- Run by
- Second Affiliated Hospital, Zhejiang University, School of Medicine
- People needed
- 30
- Starts
- 2024-12-28
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2024-12-27
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- 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;
Where it is running
- Second Affiliated Hospital of Zhejiang University — Hangzhou, Zhejiang, China (enrolling)
Full record on ClinicalTrials.gov
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