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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

A Phase I/IIa clinical study SGT003 in patients with advanced solid tumors.

調査の概要

状態

募集

介入・治療

詳細な説明

This is a first-in-human Phase I/IIa clinical study evaluating the safety, tolerability, pharmacokinetic (PK) characteristics, immunogenicity, and preliminary efficacy of SGT003 in patients with advanced solid tumors. The study comprises a Phase I (dose-escalation) stage and a Phase IIa (dose-expansion) stage.

研究の種類

介入

入学 (推定)

332

段階

  • フェーズ2
  • フェーズ 1

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。

研究連絡先

研究場所

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100142
        • 募集
        • Beijing Cancer Hospital

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Patient can fully understand the trial, participates voluntarily, and signs informed consent form (ICF) prior to any study procedures
  2. Patients aged 18 to 75 years at the time of ICF signature.
  3. 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.
  4. ECOG 0 or 1.
  5. Radiographic evidence (CT/MRI, etc.) of disease progression documented during or after the most recent prior treatment.
  6. Patients must have adequate bone marrow reserve and organ function.

Exclusion Criteria:

  1. 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.
  2. Subjects who have received systemic immunosuppressant therapy within 14 days prior to the first administration of the investigational product.
  3. Subjects receiving anticoagulants such as therapeutic-dose heparin or vitamin K antagonists.
  4. Subjects who have received any live or attenuated live vaccine within 28 days prior to the first administration of the investigational product.
  5. Subjects who have undergone major surgery within 4 weeks prior to the first administration of the investigational product.
  6. Subjects with a history of Grade ≥3 immune-related adverse events (irAEs), hypersensitivity reactions, or Grade ≥2 immune-related myocarditis.
  7. 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.
  8. 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

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: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.
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
Evaluated at each dose level of SGT003 graded by NCI CTCAE v6.0.
Within the first dose cycle (Day1-Day21) of SGT003
Phase I: Maximum Toxicity Dose(MTD)
時間枠:Within the first dose cycle (Day1-Day21) of SGT003
The MTD is based on the incidence of DLTs
Within the first dose cycle (Day1-Day21) of SGT003
Phase I: Recommended Phase II dose (RP2D)
時間枠:Within the first dose cycle (Day1-Day21) of SGT003
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
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
area under the plasma concentration-time curve
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
peak concentration
From first study treatment to EOT, average of 24 months
Time to peak concentration(Tmax)
時間枠:From first study treatment to EOT, average of 24 months
time to peak concentration
From first study treatment to EOT, average of 24 months
Immunogenicity
時間枠:Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
ADA detection rate, ADA incidence rate, Nab detection rate (if applicable), Nab incidence rate (if applicable)
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
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
The ratio of CR、PR and SD Evaluated by RECIST1.1 and iRECIST, whichever occurs first.
average Up to 24 months
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.
average up to 24 months
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
average up to 24 months

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 (実際)

2026年8月17日

一次修了 (推定)

2028年12月1日

研究の完了 (推定)

2029年6月1日

試験登録日

最初に提出

2026年8月17日

QC基準を満たした最初の提出物

2026年9月6日

最初の投稿 (実際)

2026年9月9日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月9日

QC基準を満たした最後の更新が送信されました

2026年9月6日

最終確認日

2026年9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

  • 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

いいえ

米国FDA規制機器製品の研究

いいえ

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