Clinical Trial

Efficacy And Safety Of Anti-PD-1/PD-L1 Antibodies In Combination With Bevacizumab And Metronomic Cyclophosphamide In Patients With Non-Small Cell Lung Cancer And Cutaneous Melanoma Previously Treated With Immune Checkpoint Blockade

Study acronym: reICB
Recruiting Phase 2
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Summary
This study will evaluate efficacy and safety of anti-PD-1/PD-L1 antibodies combined with bevacizumab and metronomic cyclophosphamide in patients with metastatic non-small cell lung cancer (NSCLC) and cutaneous melanoma previously treated with immune checkpoint blockade (ICB). The hypotheses of this study are that a combination of ICB, cyclophosphamide, and bevacizumab prolongs progression-free survival and overall survival, and also increases rates of objective responses and disease control.
Trial Details
NCT Number NCT07130032
Lead Sponsor EuroCityClinic LLC
Collaborators: First Pavlov State Medical University in St. Petersburg, Russia
Conditions Metastatic Non-small Cell Lung Cancer (NSCLC), Metastatic Cutaneous Melanoma
Enrollment 90 participants
Start Date 2025-08-14
Primary Completion 2025-08-14 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2025-08-19