Clinical Trial

Phase II Study of QLC2519 in Pediatric Solid Tumor Participants

Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
QLC2519 (Mai Li Sheng®) is a new protein drug created by fusing the N-terminal of highly active modified G-CSF with the C-terminal of HSA. The modified G-CSF retained high activity while reducing affinity for the G-CSF receptor, which can significantly inhibit the the G-CSF receptor-mediated (RMC) pathway. The aim of this study is to evaluate the PK/PD characteristics of QLC2519 in preventing chemotherapy-induced neutropenia (CIN) in children with sarcoma.
Trial Details
NCT Number NCT07724756
Lead Sponsor Qilu Pharmaceutical Co., Ltd.
Conditions Pediatric Malignant Solid Tumor, Febrile Neutropenia (FN), Neutropenia
Enrollment 18 participants
Start Date 2026-06-26
Primary Completion 2027-06-26 (estimated)
Study Completion 2028-06-26 (estimated)
Updated on ClinicalTrials.gov 2026-07-24