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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

2026년 9월 6일 업데이트: Beijing Sungen Biomedical Technology Co., Ltd

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.

연구 개요

상태

모병

개입 / 치료

상세 설명

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.

연구 유형

중재적

등록 (추정된)

332

단계

  • 2 단계
  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Beijing Municipality
      • Beijing, Beijing Municipality, 중국, 100142
        • 모병
        • Beijing Cancer Hospital

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

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  • 고령자

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설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Adverse Events (AEs), immune-related Adverse Events (irAEs)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Area under the plasma concentration-time curve (AUC)
기간: 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)
기간: 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)
기간: 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
기간: 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.

기타 결과 측정

결과 측정
측정값 설명
기간
Phase I. Objective Response Rate (ORR)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: average up to 24 months
the period from date of randomization to death
average up to 24 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 8월 17일

기본 완료 (추정된)

2028년 12월 1일

연구 완료 (추정된)

2029년 6월 1일

연구 등록 날짜

최초 제출

2026년 8월 17일

QC 기준을 충족하는 최초 제출

2026년 9월 6일

처음 게시됨 (실제)

2026년 9월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 9일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 6일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

키워드

기타 연구 ID 번호

  • SG-SGT003-101
  • CTR20262751 (레지스트리 식별자: China Center for Drug Evaluation (CDE), NMPA)

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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