Phase I Study of Becotatug Vedotin for Safety and Efficacy in EGFR-Positive Pediatric Relapsed/Refractory or Metastatic Solid Tumors (MRG003)
A Phase I Clinical Study to Explore the Safety and Efficacy of Becotatug Vedotin in Pediatric Patients With EGFR-Positive Relapsed/Refractory or Metastatic Solid Tumors
調査の概要
状態
条件
介入・治療
詳細な説明
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Yizhuo Zhang
- 電話番号:020-87342460
- メール:zhangyzh@sysucc.org.cn
研究場所
-
-
Guangdong
-
Guangzhou、Guangdong、中国、510060
- 募集
- Sun Yat-sen University Cancer Center
-
コンタクト:
- Yi Que
- 電話番号:020-87342460
- メール:queyi@sysucc.org.cn
-
主任研究者:
- Yizhuo Zhang
-
-
参加基準
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
説明
Inclusion Criteria:
- All participants must meet all of the following criteria to be eligible for enrollment:
Informed Consent: The patient (and/or legal guardian, as age-appropriate) fully understands the study, voluntarily agrees to participate, and signs a written informed consent form (ICF). A separate biomarker consent form is required for EGFR testing prior to screening.
Age: 2 to 18 years old at the time of consent. Life Expectancy: Estimated overall survival of at least 3 months.
Histologically Confirmed Disease: Pathologically confirmed relapsed/refractory or metastatic EGFR-positive solid tumor, belonging to one of the following subtypes:
Head and neck squamous cell carcinoma, nasopharyngeal carcinoma, or lymphoepithelial carcinoma that progressed during or after at least one line of platinum-based chemotherapy and PD-1/PD-L1 inhibitor therapy Rhabdomyosarcoma Neuroblastoma Medulloblastoma Wilms tumor Atypical teratoid/rhabdoid tumors (AT/RTs) Diffuse intrinsic pontine gliomas (DIPGs) Other EGFR-positive solid tumor subtypes deemed eligible by the investigator Measurable Disease: At least one measurable tumor lesion by computed tomography (CT) or magnetic resonance imaging (MRI) per RECIST v1.1 criteria (longest diameter ≥10 mm; pathological lymph node short axis ≥15 mm).
Performance Status: Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1, or 2.
Adequate Bone Marrow Function:
Absolute neutrophil count (ANC) ≥1.5 × 10⁹/L Platelet count ≥75 × 10⁹/L Hemoglobin ≥80 g/L Exception for patients with bone marrow involvement: ANC ≥1.0 × 10⁹/L, platelets ≥50 × 10⁹/L, hemoglobin ≥75 g/L
Adequate Hepatic and Renal Function:
Serum creatinine ≤1.5 × upper limit of normal (ULN) Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 × ULN Total bilirubin ≤1.5 × ULN Exception for patients with liver involvement: AST/ALT ≤5 × ULN, total bilirubin ≤3 × ULN
Exclusion Criteria:
- Participants will be excluded from the study if they meet any of the following criteria:
Hypersensitivity: Known hypersensitivity to any component of Becotatug Vedotin (MRG003) or its excipients.
Symptomatic CNS Metastases: Presence of symptomatic central nervous system (CNS) metastases.
Prior Malignancies: History of other primary malignant tumors, except for:
Locally excised basal cell or squamous cell carcinoma of the skin Cervical carcinoma in situ Any prior malignancy that has been in complete remission for ≥3 years without treatment Note: Melanoma (any stage) is explicitly excluded
Significant Liver Disease: Clinically significant liver disease, including:
Positive hepatitis C virus (HCV) antibody Chronic active hepatitis B (HBV DNA >20,000 IU/mL) HIV Infection: Known human immunodeficiency virus (HIV) infection. Severe Ocular Abnormalities: History of severe ophthalmologic conditions, such as severe dry eye syndrome or exposure keratitis.
Uncontrolled Systemic Diseases: Severe or uncontrolled medical conditions, including:
Interstitial lung disease or pneumonitis Active autoimmune diseases requiring systemic immunosuppressive therapy
Cardiac Disease: Clinically significant cardiac dysfunction or cardiac disease, including:
Congestive heart failure (New York Heart Association Class ≥II) Uncontrolled arrhythmias QTc interval prolongation >450 ms (males) or >470 ms (females) Recent Antitumor Therapy: Received any systemic antitumor therapy (chemotherapy, biological therapy, immunotherapy, targeted therapy) within 3 weeks prior to the first dose of study drug, and have not recovered to CTCAE v4.03 Grade ≤1 (except alopecia).
Recent Major Surgery: Underwent major surgical procedure within 3 weeks prior to the first dose of study drug.
Planned Surgery: Planned surgical procedure during the study period, or any surgery deemed necessary by the investigator.
Prior EGFR Therapy Toxicity: History of severe skin toxicity caused by prior EGFR-targeted therapy, or chronic skin disease requiring ongoing oral or intravenous treatment.
Other Significant Risks: Any other concurrent medical condition that, in the investigator's judgment, would increase the risk of toxicity or compromise the patient's ability to complete the study.
研究計画
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:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- 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 |
|---|---|
|
実験的:Becotatug Vedotin (MRG003) Phase I Dose-Escalation & Expansion in EGFR-Positive Pediatric R/M Solid
This is a single-arm, open-label study where all enrolled participants receive Becotatug Vedotin (MRG003), a novel EGFR-targeted antibody-drug conjugate (ADC), as monotherapy. Intervention Details Study Drug: Becotatug Vedotin (MRG003) for Injection Route of Administration: Intravenous (IV) infusion over 30 minutes to 3 hours Dosing Schedule: Every 3 weeks (Q3W) on Day 1 of each 21-day cycle Maximum Treatment Duration: Up to 8 cycles (24 weeks) Dose Levels: Ia Dose-Escalation Phase: 4 planned dose levels (1.0, 1.5, 2.0, 2.3 mg/kg) Starting dose: 1.0 mg/kg (modified accelerated titration design, 1 patient per cohort) Subsequent doses: Standard 3+3 design Ib Dose-Expansion Phase: All patients receive the determined Recommended Phase II Dose (RP2D) |
Study Drug: Becotatug Vedotin (MRG003) for Injection (lyophilized powder, 20 mg/vial) Route: Intravenous (IV) infusion over 30 minutes to 3 hours Schedule: Every 3 weeks (Q3W) on Day 1 of each 21-day cycle Maximum Treatment Duration: Up to 8 cycles (24 weeks); patients with confirmed clinical benefit (objective response or stable disease) may continue treatment beyond 8 cycles until disease progression, unacceptable toxicity, withdrawal of consent, or study termination
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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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Incidence of dose-limiting toxicities
時間枠:First 21-day treatment cycle (Cycle 1)
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DLTs are defined as treatment-related adverse events or laboratory abnormalities (excluding hypersensitivity reactions) that meet CTCAE v4.03 grade 3-4 criteria and occur during the first 21 days of treatment, including:
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First 21-day treatment cycle (Cycle 1)
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
- 泌尿生殖器疾患
- 顎口腔疾患
- 病理学的プロセス
- 泌尿生殖器腫瘍
- 部位別新生物
- 新生物
- 男性の泌尿生殖器疾患
- 腎臓病
- 泌尿器疾患
- 女性の泌尿生殖器疾患
- 女性の泌尿生殖器疾患と妊娠合併症
- 疾患の属性
- 遺伝性疾患、先天性疾患
- 組織型別の新生物
- 頭頸部腫瘍
- 新生物、腺および上皮
- 腫瘍性プロセス
- 泌尿器科の新生物
- がん
- 耳鼻咽喉科疾患
- 神経膠腫
- 新生物、神経上皮
- 神経外胚葉性腫瘍
- 新生物、生殖細胞および胚
- 新生物、神経組織
- 腎腫瘍
- 腫瘍性症候群、遺伝性
- 咽頭腫瘍
- 耳鼻咽喉科の新生物
- 上咽頭疾患
- 咽頭疾患
- 肉腫
- 新生物、結合組織および軟部組織
- 神経外胚葉性腫瘍、原始、末梢
- 原始神経外胚葉性腫瘍
- 新生物、筋組織
- がん、扁平上皮細胞
- 複合型および混合型の新生物
- 筋肉腫
- 上咽頭腫瘍
- 先天性、遺伝性、および新生児の疾患と異常
- 病理学的状態、徴候および症状
- 上咽頭がん
- 頭頸部の扁平上皮がん
- 再発
- 新生物転移
- 神経芽細胞腫
- 横紋筋肉腫
- 髄芽腫
- ウィルムス腫瘍
- ラブドイド腫瘍
その他の研究ID番号
- MRG003-pediatirc-001
- Sun Yat-sen University Cancer (その他の識別子:Sun Yat-sen University Cancer)
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?
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
米国FDA規制機器製品の研究
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