A First-in-Human Study of CKD-703 in Advanced Solid Tumors and 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: CKD-703.
- Кому может быть актуально
- Состояния в реестре: Advanced Solid Tumors, Non-Small Cell Lung Cancer. Базовые параметры: от 19 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
- 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 First-in-Human, Multicenter, Open-Label, Phase 1/2a Study to Evaluate the Safety, Efficacy and Pharmacokinetics of CKD-703 in Advanced c-Met Expressing Solid Tumors, and in MET Amplified and c-Met Overexpressing Non-Small Cell Lung Cancer
Обзор
This is a Phase 1/2a open-label multicenter study to evaluate the safety, efficacy, and pharmacokinetics of CKD-703 in Advanced c-Met Expressing Solid Tumors, and in MET-Amplified and c-Met Overexpressing Non-Small Cell Lung Cancer. CKD-703 is composed of a c-Met-targeting monoclonal antibody (mAb) coupled to a cytotoxic payload consisting of the anti-microtubule drug monomethyl auristatin E (MMAE); thus, CKD-703 is a novel ADC offering a highly targeted approach with potential improvement of efficacy while reducing off-target effects for patients with NSCLC and other cancers.
Вмешательства
- Препарат CKD-703
Intravenous (IV) Infusion
Первичные конечные точки
- Part 1: Number of patients with dose limiting toxicity (DLT) [Срок оценки: first 21-day period of therapy]
- Part 2 and Part 3: Object Response Rate (ORR) [Срок оценки: Up to 24 months]
Вторичные конечные точки (10)
- All parts : Treatment-Emergent Adverse Events (TEAE) [Срок оценки: Up to 24 months]
- All parts : Immunogenicity (ADA) [Срок оценки: Up to 24 months]
- All parts : Immunogenicity (NAb) [Срок оценки: Up to 24 months]
- Part 1 and Part 2 : Pharmacokinetic parameter [Срок оценки: Up to 24 months]
- Part 1 and Part 2 : Pharmacokinetic parameter [Срок оценки: Up to 24 months]
- Part 1 and Part 2 : Pharmacokinetic parameter [Срок оценки: Up to 24 months]
- Part 1 and Part 3 : Best Overall Response (BOR) [Срок оценки: Up to 24 months]
- All parts : Duration of Response (DoR) [Срок оценки: Up to 24 months]
- Part 2 and Part 3 : Progression-Free Survival (PFS) [Срок оценки: Up to 24 months]
- Part 2 and Part 3 : Overall Survival (OS) [Срок оценки: Up to 24 months]
Критерии участия
Критерии включения
- Males and females ≥ 19-year-old
- Part 1 : Solid tumors including NSCLC for which standard therapy has failed or was not tolerated, and no other effective therapy exists
- Part 2 : Histologically or cytologically documented c-Met overexpressing nonsquamous NSCLC having failed at least 1 line of SoC therapy (platinum-based chemotherapy and/or immune checkpoint inhibitor).
- Part 3 : Histologically or cytologically documented c-Met expressing solid tumors for which standard therapy has failed or was not tolerated.
- In all parts of the study, subjects with NSCLC with documented actionable genetic alterations must have failed at least 1 line of country-level approved targeted therapies
- Life expectancy ≥ 12 weeks as judged by the Investigator
- Documented progressive and measurable disease as defined by RECIST 1.1
- ECOG Performance Status 0 or 1
Критерии исключения
- Subject has received radiation therapy to the lung < 6 months prior to the first dose of study drug
- Prior radiotherapy to ≥ 25% of bone marrow
- Anticancer systemic therapy such as immunotherapy, biologic, cytotoxic chemotherapy, or any investigational therapy (including cell therapy or gene therapy) within a period of 28 days prior to the first dose of study drug. Any anticancer therapy small molecule (eg. kinase inhibitor) or herbal therapy within 14 days prior to the first dose of study drug
- Prior c-Met-targeted antibody therapy or any MMAE-containing ADC (prior c-Met targeting small molecules are allowed)
- Use of strong P-gp and/or CYP3A4/5 inducers within 21 days prior or strong P-gp and/or CYP3A4/5 inhibitors within 14 days prior to the first dose of study drug
- Use of sensitive CYP3A4/5 substrate within 3 days or 5 times half-life prior to the first dose of study drug.
- Evidence of pulmonary fibrosis on screening imaging assessment or any history of pneumonitis that required treatment with systemic steroids within 12 months of the planned first dose of the study drug
- History of drug induced interstitial lung disease
- Prior or active ocular or corneal disease based on ophthalmic evaluation (slit lamp and visual acuity)
- Prior Grade 3 neuropathy or chronic Grade 2 neuropathy
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Нерандомизированное
- Модель
- Последовательный дизайн
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
США · 1 центр
- Gabrail Cancer Center — Ohio City
Идентификаторы
NCT: NCT07439094 · A161_01ST/NSCLC2503