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Набор скоро начнётся NCT07046780

A Multicenter, Prospective, Non-Interventional Real-World Study of Iparomlimab and Tuvonralimab Injection (QL1706) in the Treatment of Locally Advanced or Metastatic Solid Tumors

— Наблюдательное Solid Tumor Cancer Metastatic Solid Tumors Locally Advanced

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Observation arm.
Кому может быть актуально
Состояния в реестре: Solid Tumor Cancer, Metastatic Solid Tumors, Locally Advanced. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Китай
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Обзор

This study is a prospective, observational, real-world, multi-center study planning to enroll 90 patients. The study will observe and document patients' actual clinical practices in receiving Iparomlimab and Tuvonralimab Injection (QL1706). The primary objectives are to evaluate the safety and effectiveness of Iparomlimab and Tuvonralimab Injection (QL1706) in treating locally advanced or metastatic solid tumors.

Вмешательства

  • Препарат Observation arm
    To observe the efficacy and safety of Iparomilimab and Tuvonralimab in the treatment of patients with solid tumors in the real world

Первичные конечные точки

  • Incidence of Grade ≥3 irAEs [Срок оценки: 2 years]
Вторичные конечные точки (3)
  • Incidence of adverse events [Срок оценки: 2 years]
  • Incidence of treatment-related adverse events [Срок оценки: 2 years]
  • Incidence of immune-related adverse events [Срок оценки: 2 years]

Критерии участия

Критерии включения

  • 1\) Histologically or cytologically confirmed locally advanced or metastatic solid tumors with disease progression (radiographic or clinical) after ≥1 line of prior standard therapy, unsuitable for/intolerant to standard therapy. Includes but not limited to: Gastrointestinal tumors (colorectal cancer, hepatocellular carcinoma, esophageal cancer, biliary tract cancer, pancreatic cancer, gastric cancer), Breast cancer, Non-small cell lung cancer (NSCLC), Small cell lung cancer (SCLC), Soft tissue sarcoma;
  • 2\) ECOG performance status 0-2;
  • 3\) ≥1 measurable lesion per RECIST v1.1 ;
  • 4\) Adequate organ function meeting ALL criteria below:
  • Hematology (without transfusion/G-CSF support within 7 days):

Absolute neutrophil count (ANC) ≥1.5×10⁹/L Platelets ≥100×10⁹/L Hemoglobin ≥90 g/L

  • Biochemistry :

Total bilirubin (TBIL) ≤2×ULN ALT/AST ≤2.5×ULN (≤5×ULN if liver metastases present) Serum creatinine (Cr) ≤1.5×ULN Albumin ≥28 g/L

  • Urinalysis :

Urine protein <2+ (dipstick) If protein ≥2+, 24h urinary protein ≤1.0 g

  • Coagulation (without anticoagulants):

PT/APTT/INR ≤1.5×ULN

  • 5\) Life expectancy ≥12 weeks;
  • 6\) Contraception : Females of childbearing potential or males with partners of childbearing potential must use effective contraception during treatment and for 6 months post-treatment;
  • 7\) Signed informed consent and protocol compliance.

Критерии исключения

  • 1\) Tumor-Related Conditions
  • Known CNS metastases (except those radiologically stable ≥4 weeks after radiotherapy);
  • Other malignancies within past 5 years, excluding:

Cured basal/squamous cell skin cancer Localized low-risk prostate cancer Cervical/breast carcinoma in situ

  • Severe bone lesions from metastatic disease, including:

Uncontrolled bone pain Pathologic fractures at critical sites (within 6 months) or impending spinal cord compression;

  • Uncontrolled effusions requiring recurrent drainage (pleural/pericardial/ascites), per investigator assessment.
  • 2\) Prior Anti-tumor Therapy
  • Prior systemic therapy with CTLA-4 inhibitors or other ICIs;
  • Any anti-tumor treatment within 4 weeks before first dose, including:

Surgery/chemotherapy/palliative radiotherapy to non-target lesions/hormonal/targeted/biologic/immunotherapy;

  • Treatment-related toxicities not recovered to CTCAE grade ≤1 (exceptions: alopecia/platinum-induced neuropathy ≤ grade 2).
  • 3\) Comorbidities \& History
  • Arterial thromboembolism within 6 months (MI/unstable angina/stroke/TIA);
  • Symptomatic heart failure (NYHA class III-IV), unstable angina, or uncontrolled arrhythmia;
  • Severe pulmonary disease : ILD/COPD/symptomatic bronchospasm;
  • Active uncontrolled infection (≥CTCAE grade 2), including:

HIV Active HBV (DNA ≥500 IU/mL) HCV (Ab+ with detectable RNA) HBV/HCV co-infection;

  • History of neurologic/psychiatric disorders;
  • Recent or current substance abuse;
  • Prior allogeneic organ/hematopoietic stem cell transplantation.
  • 4\) Hypersensitivity to study drug or its excipients.
  • 5\) Active autoimmune disease requiring treatment or history within 2 years. Exceptions: Vitiligo/alopecia/psoriasis not needing systemic therapy Hypothyroidism managed only with hormone replacement Type 1 diabetes controlled solely with insulin.
  • 6\) Pregnant/lactating women;
  • 7\) Any uncontrolled systemic disease increasing study risk (per investigator);
  • 8\) Other unsuitable conditions determined by investigator.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Китай · 1 центр
  • Cancer Hospital, Chinese Academy of Medical Sciences — Пекин

Идентификаторы

NCT: NCT07046780 · NCC5416

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗