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Phase II Study of QLC2519 in Pediatric Solid Tumor Participants

20 juli 2026 bijgewerkt door: Qilu Pharmaceutical Co., Ltd.

A Multicenter, Open-label Phase II Clinical Study Evaluating the Pharmacokinetics, Pharmacodynamics, Safety, and Efficacy of Albipagrastim Alfa for Injection (QLC2519) in Pediatric Solid Tumor Participants

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.

Studie Overzicht

Gedetailleerde beschrijving

This study is a multicenter, open lable Phase II study planed to enroll 18 children with pediatric sarcoma. The participants will receive the VDC/IE chemotherapy regimen (VDC: vincristine, doxorubicin, cyclophosphamide; IE: ifosfamide, etoposide) and will be scheduled to undergo 3 chemotherapy cycles (21 days per cycle). The participants will be stratified by age (<6 years, 6 to <12 years, 12 to <18 years), with enrollment progressing from the older to the younger age groups (6 in each group).

Studietype

Ingrijpend

Inschrijving (Geschat)

18

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Beijing, China
        • Werving
        • Beijing Children's Hospital
        • Contact:
          • Beijing Children's Hospital Beijing Children's Hospital
          • Telefoonnummer: 01058531216
          • E-mail: bcec_ist@bch.com.cn

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Kind
  • Volwassen

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Age 0-18 years (excluding boundary values), any gender;
  • Participant diagnosed with pediatric sarcoma based on pathological histology;
  • Participant was suitable for receiving the VDC/IE chemotherapy regimen, and planning to receive at least 3 chemotherapy cycles (VDC: vincristine, doxorubicin, cyclophosphamide; IE: ifosfamide, etoposide);
  • ECOG ≤1;
  • Expected survival ≥3 months, and expected to complete the 3 chemotherapy cycles specified in the regimen;
  • Hematology, liver function, and renal function before the first administration of chemotherapy drugs meet the following requirements:
  • Hematology: absolute neutrophil count (ANC) in peripheral blood ≥2.0×10^9/L (or above the lower limit of normal); platelet count (PLT) ≥100×10^9/L; hemoglobin (HGB) ≥90 g/L; white blood cell count (WBC) ≥4.0×10^9/L;
  • Liver function: total bilirubin (TBIL) ≤1.5×ULN, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤1.5×ULN; for patients with liver metastasis, ALT and AST ≤2.5×ULN;
  • Renal function: serum creatinine (Cr) ≤1.5×ULN or creatinine clearance rate (CCr) ≥60 mL/min;
  • Normal bone marrow hematopoietic function, no bleeding tendency (INR <1.5);
  • Female participants of potential reproductive ability (post-menarche) are neither pregnant nor breastfeeding; participants of potential reproductive ability (e.g., females post-menarche or males post-spermarche) must agree to use effective contraception from the time of signing the informed consent until at least 3 months after the last administration.

Exclusion Criteria:

  • Tumor had metastasized to or invaded the bone marrow;
  • Previously received chemotherapy or radiotherapy;
  • Planned surgery or radiotherapy during the trial (excluding the follow-up period);
  • Presence of other malignant tumors besides sarcoma (participants with previously cured malignant tumors with no recurrence within the past 5 years may be included in this study);
  • Primary central nervous system tumor or existing central nervous system involvement, or suspected central nervous system metastasis based on clinical manifestations, deemed unsuitable for participation in this study by the investigator;
  • History of primary hematologic diseases, including but not limited to leukemia, myelodysplastic syndromes, aplastic anemia, sickle cell anemia, congenital neutropenia, or cyclic neutropenia;
  • Previously received or planned to undergo bone marrow transplantation, hematopoietic stem cell transplantation, or organ transplantation during the trial;
  • Diseases with severe cardiac dysfunction, including but not limited to poorly controlled arrhythmia or heart failure;
  • Diseases with severe pulmonary dysfunction, including but not limited to pulmonary embolism, lung abscess, or acute respiratory distress syndrome;
  • Presence of splenomegaly or diseases that may cause splenomegaly (such as liver cirrhosis, Gaucher disease, glycogen storage disease, Niemann-Pick disease, etc.), considered unsuitable for participation in this study by the investigator;
  • Presence of acute infectious disease or chronic infectious disease in the active phase at screening, such as hepatitis B patients who are hepatitis B surface antigen (HbsAg) positive with detectable HBV-DNA indicating viral replication, hepatitis C patients who are anti-HCV antibody positive with detectable HCV-RNA indicating viral replication; positive syphilis screening (positive specific antibody test, negative nonspecific antibody test, and confirmed as non-active infection based on clinical judgment is excluded);
  • History of human immunodeficiency virus (HIV) infection, or HIV positive at screening;
  • Undergoing major surgery within 1 month prior to screening (high-risk, complex, or difficult procedures, such as thoracoscopic pulmonary bulla resection or thoracoscopic esophageal atresia surgery);
  • Received or planned to use recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) within 1 week prior to screening or during the trial;
  • Received glucocorticoid (oral or intravenous) or lithium treatment within 1 week prior to screening;
  • Received whole blood, white blood cells, or platelet transfusion within 2 weeks prior to screening;
  • Received human granulocyte colony-stimulating factor (G-CSF) treatment within 3 months prior to screening;
  • Received systemic anti-infective therapy (oral or intravenous) within 72 hours prior to screening;
  • History of drug or alcohol abuse, or history of substance abuse;
  • Received other clinical trial drugs or treatments within 4 weeks prior to screening;
  • History of allergic diseases, being of an allergic constitution, or known allergy to any drug or component of this trial.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Preventie
  • Toewijzing: NVT
  • Interventioneel model: Sequentiële toewijzing
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Treatment Group

Chemotherapy C1&3:

Changchun Shinkai (V): 1.5 mg/m² (maximum dose 2 mg), iv, on D1, 8, and 15; Doxorubicin (D): 30 mg/m², iv over more than 6 hours, on D1 and 2; Cyclophosphamide (C): 1.2 g/m², iv over more than 1 hour, on D1; Mesna: 360 mg/(m²/dose), iv, at 0, 3, 6, and 9 hours during cyclophosphamide.

Chemotherapy C2:

Ifosfamide (I): 1.8 g/m², iv over more than 1 hour, QD for 5 days (D1~D5); Etoposide (E): 100 mg/m², iv over more than 4 hours, QD for 5 days (D1~D5); Mesna: 360 mg/(m²/dose), iv, at 0, 3, 6, 9 hours during ifosfamide.

QLC2519 500 μg/kg was administered 48 hours after chemotherapy (generally on D4 of the first and third chemotherapy cycles, and on D7 of the second cycle, between 6:00 and 10:00 AM), once per chemotherapy cycle.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Cmax of QLC2519
Tijdsspanne: At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
Maximum (peak) serum concentration (Cmax) of QLC2519 will be reported.
At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
AUC0-t of QLC2519
Tijdsspanne: At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
Area Under the Curve from time zero to time t (AUC0-t) of QLC2519 will be reported.
At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
Time to start administering chemotherapy drugs until the nadir of absolute neutrophil count (ANC)
Tijdsspanne: At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Duration and incidence of severe ANC reduction
Tijdsspanne: At treatment cycle 1 to cycle 3 (cycle length = 21 days)
ANC < 0.5 × 10⁹/L
At treatment cycle 1 to cycle 3 (cycle length = 21 days)
Efficacy: Incidence of febrile neutropenia (FN)
Tijdsspanne: At treatment cycle 1 to cycle 3 (cycle length = 21 days)
At treatment cycle 1 to cycle 3 (cycle length = 21 days)
Duration and incidence of ANC < 1.0 × 10^9/L
Tijdsspanne: At treatment cycle 1 to cycle 3 (cycle length = 21 days)
At treatment cycle 1 to cycle 3 (cycle length = 21 days)
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
Tijdsspanne: Up to Week 14
Up to Week 14

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

26 juni 2026

Primaire voltooiing (Geschat)

26 juni 2027

Studie voltooiing (Geschat)

26 juni 2028

Studieregistratiedata

Eerst ingediend

29 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

20 juli 2026

Eerst geplaatst (Werkelijk)

24 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

24 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

20 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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