Phase II Study of QLC2519 in Pediatric Solid Tumor Participants
2026年7月20日 更新者: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.
調査の概要
詳細な説明
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).
研究の種類
介入
入学 (推定)
18
段階
- フェーズ2
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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Beijing、中国
- 募集
- Beijing Children's Hospital
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コンタクト:
- Beijing Children's Hospital Beijing Children's Hospital
- 電話番号:01058531216
- メール:bcec_ist@bch.com.cn
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 子
- 大人
健康ボランティアの受け入れ
いいえ
説明
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.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:防止
- 割り当て:なし
- 介入モデル:順次割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Cmax of QLC2519
時間枠:At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
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Maximum (peak) serum concentration (Cmax) of QLC2519 will be reported.
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At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
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AUC0-t of QLC2519
時間枠:At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
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Area Under the Curve from time zero to time t (AUC0-t) of QLC2519 will be reported.
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At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
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Time to start administering chemotherapy drugs until the nadir of absolute neutrophil count (ANC)
時間枠:At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
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At treatment Cycle 1 and Cycle 3 (cycle length = 21 days)]
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Duration and incidence of severe ANC reduction
時間枠:At treatment cycle 1 to cycle 3 (cycle length = 21 days)
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ANC < 0.5 × 10⁹/L
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At treatment cycle 1 to cycle 3 (cycle length = 21 days)
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Efficacy: Incidence of febrile neutropenia (FN)
時間枠:At treatment cycle 1 to cycle 3 (cycle length = 21 days)
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At treatment cycle 1 to cycle 3 (cycle length = 21 days)
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Duration and incidence of ANC < 1.0 × 10^9/L
時間枠:At treatment cycle 1 to cycle 3 (cycle length = 21 days)
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At treatment cycle 1 to cycle 3 (cycle length = 21 days)
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Number of Participants With Treatment-emergent Adverse Events (TEAEs)
時間枠:Up to Week 14
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Up to Week 14
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
2026年6月26日
一次修了 (推定)
2027年6月26日
研究の完了 (推定)
2028年6月26日
試験登録日
最初に提出
2026年6月29日
QC基準を満たした最初の提出物
2026年7月20日
最初の投稿 (実際)
2026年7月24日
学習記録の更新
投稿された最後の更新 (実際)
2026年7月24日
QC基準を満たした最後の更新が送信されました
2026年7月20日
最終確認日
2026年7月1日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- QLC2519-201
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
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