A Phase I/IIa Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, Immunogenicity, and Preliminary Efficacy of SGT003 in Patients With Advanced Solid Tumors
A Multicenter, Dose-Escalation and Expansion Phase I/IIa Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, Immunogenicity, and Preliminary Efficacy of SGT003 in Patients With Advanced Solid Tumors
調査の概要
詳細な説明
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Shuchang Jiang
- 電話番号:+86 13552250017
- メール:shuchang.jiang@hotgen.com.cn
研究場所
-
-
Beijing Municipality
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Beijing、Beijing Municipality、中国、100142
- 募集
- Beijing Cancer Hospital
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-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Patient can fully understand the trial, participates voluntarily, and signs informed consent form (ICF) prior to any study procedures
- Patients aged 18 to 75 years at the time of ICF signature.
Study population:
- Phase I (dose-escalation study): Patients with advanced solid tumors confirmed histologically or cytologically, who have failed at least one standard therapy for advanced disease, are intolerant to standard therapy, or have no available standard treatment options.
- Phase IIa (dose-expansion study): Patients with advanced solid tumors who have received at least first-line but not up to third-line standard systemic therapy and experienced disease progression or intolerance to such therapy.
- ECOG 0 or 1.
- Radiographic evidence (CT/MRI, etc.) of disease progression documented during or after the most recent prior treatment.
- Patients must have adequate bone marrow reserve and organ function.
Exclusion Criteria:
- Subjects who have received chemotherapy, radiotherapy, biotherapy, endocrine therapy, immunosuppressive therapy or other anti-tumor therapy within 4 weeks prior to the first administration of the investigational product.
- Subjects who have received systemic immunosuppressant therapy within 14 days prior to the first administration of the investigational product.
- Subjects receiving anticoagulants such as therapeutic-dose heparin or vitamin K antagonists.
- Subjects who have received any live or attenuated live vaccine within 28 days prior to the first administration of the investigational product.
- Subjects who have undergone major surgery within 4 weeks prior to the first administration of the investigational product.
- Subjects with a history of Grade ≥3 immune-related adverse events (irAEs), hypersensitivity reactions, or Grade ≥2 immune-related myocarditis.
- Subjects with active autoimmune disease or prior autoimmune disease with a risk of recurrence. Exceptions: well-controlled type 1 diabetes, hypothyroidism controlled solely by hormone replacement therapy, and skin diseases that do not require systemic treatment.
- Subjects with current or prior active interstitial lung disease (ILD). Subjects with radiation-induced pulmonary fibrosis that does not require steroid therapy are eligible.
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:SGT003
Use SGT003 for Injection
|
Dosage Form: Injection Strength: 50 mg (5 mL) per vial Dosage and Administration: Subjects will receive SGT003 (investigational product) via intravenous (IV) infusion on Day 1 (D1) of each cycle. Dose: During the Phase I dose-escalation, subjects will be dosed according to the assigned dose cohort; during the Phase IIa dose-expansion stage, subjects will be dosed according to the selected expansion dose. Duration of Administration: For each subject, the first infusion will be completed within 90 minutes. If no infusion-related reaction (IRR) and/or hypersensitivity reaction occurs, the subsequent infusion duration may be shortened to no less than 60 minutes. |
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 |
|---|---|---|
|
Adverse Events (AEs), immune-related Adverse Events (irAEs)
時間枠:First dose up to 28 days (+3 days) after EOT, or prior to initiation of other anti-tumor therapy, whichever occurs first.
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This includes clinically significant changes in vital signs, physical examination, electrocardiogram, echocardiogram and clinical laboratory tests, as graded by National Cancer Institute (NCI) Common Terminology for Adverse Events (CTCAE) version 6.0.
|
First dose up to 28 days (+3 days) after EOT, or prior to initiation of other anti-tumor therapy, whichever occurs first.
|
|
Phase I: Dose Limit Toxicity (DLTs)
時間枠:Within the first dose cycle (Day1-Day21) of SGT003
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Evaluated at each dose level of SGT003 graded by NCI CTCAE v6.0.
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Within the first dose cycle (Day1-Day21) of SGT003
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Phase I: Maximum Toxicity Dose(MTD)
時間枠:Within the first dose cycle (Day1-Day21) of SGT003
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The MTD is based on the incidence of DLTs
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Within the first dose cycle (Day1-Day21) of SGT003
|
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Phase I: Recommended Phase II dose (RP2D)
時間枠:Within the first dose cycle (Day1-Day21) of SGT003
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The RP2D is based on the results of safety、PK/PD and preliminary efficacy of SGT003 in the stage of dose escalation
|
Within the first dose cycle (Day1-Day21) of SGT003
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Phase IIa: Objective Response Rate (ORR)
時間枠:from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first. average Up to 24 months
|
The ratio of CR and PR Evaluated by RECIST1.1 and iRECIST,
|
from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first. average Up to 24 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Area under the plasma concentration-time curve (AUC)
時間枠:From first study treatment to EOT, average of 24 months
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area under the plasma concentration-time curve
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From first study treatment to EOT, average of 24 months
|
|
Peak concentration (Cmax)
時間枠:From first study treatment to EOT, average of 24 months
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peak concentration
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From first study treatment to EOT, average of 24 months
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Time to peak concentration(Tmax)
時間枠:From first study treatment to EOT, average of 24 months
|
time to peak concentration
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From first study treatment to EOT, average of 24 months
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Immunogenicity
時間枠:Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
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ADA detection rate, ADA incidence rate, Nab detection rate (if applicable), Nab incidence rate (if applicable)
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Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Phase I. Objective Response Rate (ORR)
時間枠:average Up to 24 months
|
Evaluated by RECIST1.1 and iRECIST, from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
|
average Up to 24 months
|
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Phase I and phase IIa. Duration of Response (DOR)
時間枠:average Up to 24 months
|
Evaluated by RECIST1.1 and iRECIST, from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
|
average Up to 24 months
|
|
Phase I and phase IIa. Disease Control Rate (DCR)
時間枠:average Up to 24 months
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The ratio of CR、PR and SD Evaluated by RECIST1.1 and iRECIST, whichever occurs first.
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average Up to 24 months
|
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Phase I and phase IIa. Time to Response (TTR)
時間枠:average up to 24 months
|
The period from the date of randomization to the occurrence of CR/PR,evaluated by RECIST1.1 and iRECIST, , until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
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average up to 24 months
|
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Phase I and phase IIa. Progression-Free Survival (PFS)
時間枠:average Up to 24 months
|
from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
Evaluated by RECIST1.1 and iRECIST,
|
average Up to 24 months
|
|
Phase IIa. Overall Survival (OS)
時間枠:average up to 24 months
|
the period from date of randomization to death
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average up to 24 months
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
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
キーワード
その他の研究ID番号
- SG-SGT003-101
- CTR20262751 (レジストリ識別子:China Center for Drug Evaluation (CDE), NMPA)
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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