Идёт набор NCT05168566

Study to Evaluate Sutetinib Maleate Capsule in Locally Advanced or Metastatic Non-small Cell Lung Cancer

Фаза II С лечением Non-small Cell Lung Cancer

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: Sutetinib Maleate Capsule.
Кому может быть актуально: Состояния в реестре: Non-small Cell Lung Cancer. 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: США, Китай
Следующий шаг: Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

A Multicenter, Open-label, Phase IIb Study to Evaluate the Efficacy and Safety of Sutetinib Maleate Capsule in Locally Advanced or Metastatic NSCLC (Non-resistant Uncommon EGFR Mutations Only, Including L861Q, G719X, and/or S768I)

Обзор

This is a Phase 2b, multicenter, open-label study to evaluate the safety and efficacy of Sutetinib Maleate Capsule in Locally Advanced or Metastatic NSCLC (Non-resistant Uncommon EGFR Mutations Only, Including L861Q, G719X, and/or S768I)

Подробное описание

Sutetinib is an investigational irreversible EGFR tyrosine kinase inhibitor. EGFR is a gene that makes a protein that is involved in cell growth and cell survival. Mutated (changed) forms of the EGFR gene and protein have been found in some types of cancer, including non-small cell lung cancer. These changes may cause cancer cells to grow and spread in the body. The purpose of this study is to explore how effective Sutetinib maleate capsules are for the treatment of patients with locally advanced or metastatic NSCLC with non-resistant uncommon EGFR mutations

Вмешательства

Препарат Sutetinib Maleate Capsule
Study drug to be taken orally with or without food (with food preferred) for up to13 cycles

Первичные конечные точки

Assessment of Objective response rate (ORR) [Срок оценки: 2 Years]

Вторичные конечные точки (11)

Assessment of Duration of response (DoR) [Срок оценки: 2 Years]
Assessment of Disease control rate (DCR) [Срок оценки: 2 Years]
Assessment of Progression free survival (PFS) [Срок оценки: 2 Years]
Assessment of Time to progressive disease [Срок оценки: 2 Years]
Assessment of Time to response [Срок оценки: 2 Years]
Assessment of Time to treatment failure (TTF) [Срок оценки: 2 Years]
Assessment of Overall survival (OS) [Срок оценки: 2 Years]
Assessment of 1-year progression-free survival [Срок оценки: 1 Year]
Assessment of 1-year survival [Срок оценки: 1 Years]
Assess incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]). [Срок оценки: 2 Years]
Assessment of Peak Plasma Concentration (Cmax) or Area under the plasma concentration versus time curve (AUC) [Срок оценки: 2 Years]

Критерии участия

Критерии включения

Age 18 years old and above, male or female.
Histopathological and/or cytopathological confirmation of locally advanced or metastatic NSCLC patients with ≤ 1 prior line of chemotherapy.
Confirmation that the tumor harbors a non-resistant uncommon EGFR mutation (tumor tissue biopsy), including one or more of L861Q, G719X and S768I mutations, excluding any other EGFR sensitive mutations and/or oncogenes..
At least one measurable lesion.
ECOG score of 0, 1, or 2.
A minimum life expectancy of > 3 months.
Adequate bone marrow reserve, hepatic, renal and coagulation function.
Willingness of all subjects of childbearing potential to use acceptable methods of birth control.

Критерии исключения

Ever used the epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) for anti-tumor therapy prior to enrollment.
Any systemic anti-tumor therapy such as chemotherapy, immunotherapy and radiation therapy used within 4 weeks prior to enrollment; any palliative radiotherapy for non-target lesions used to relieve symptoms and traditional Chinese medicines indicated for tumor within 2 weeks prior to enrollment.
Use or intake of drugs or foods containing potent inhibitor or inducer of cytochrome P450 isozyme 3A4 (CYP3A4) within 14 days or 5 half-lives, whichever was the longer, prior to enrollment.
Surgical operation (excluding aspiration biopsy) of main organs or a significant injury within 4 weeks prior to enrollment.
Any unresolved toxicities from prior therapy greater than Grade 1 at the time of screening except alopecia.
Inability to swallow the study medication, any seriously chronic gastrointestinal disorder, malabsorption syndrome or any other conditions with influence on gastrointestinal absorption.
Active central nervous system metastases
Previous or current interstitial lung disease, radiation pneumonitis which requires hormone therapy, or drug-related pneumonia, idiopathic interstitial pulmonary fibrosis identified in a baseline CT scan; uncontrolled massive pleural or pericardial effusion.
Any active infection which has not been controlled at screening.
Any serious cardiovascular disease.
History of other serious systemic disease not suitable for clinical trial.
Participation in other interventional clinical trial 4 weeks prior to enrollment or within 5 half-lives from the last dose of investigational product (whichever is longer).
Known alcohol or drug dependence.
Mental disorders or poor compliance.
Previously received solid organ transplantation or hematopoietic stem cell transplantation.
Females who are pregnant or breastfeeding.
Known hypersensitivity to the active ingredients or excipients of the investigational product.
Have any other primary malignant tumors within 3 years (except some low- risk cancers).