- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04941339
A Study of MRG002 in the Treatment of Patients With HER2-positive Advanced Solid Tumors
2 de diciembre de 2021 actualizado por: Shanghai Miracogen Inc.
A Phase I, Open-label, Multi-center, First in Human, Dose Escalation and Expansion Study to Assess the Safety, Tolerability, Efficacy and Pharmacokinetics of MRG002 in Patients With HER2 Positive Advanced Solid Tumors
The objective of this study is to assess the safety, efficacy, pharmacokinetics, and immunogenicity of MRG002 in patients with HER2-positive advanced solid tumors.
Descripción general del estudio
Descripción detallada
This study consists of two parts.
Phase Ia is a dose escalation study to determine the maximum tolerated dose (MTD) and recommended phase II dose (RP2D) of MRG002.
Phase Ib is a dose expansion study to further assess the efficacy and safety of MRG002 at confirmed RP2D.
Tipo de estudio
Intervencionista
Inscripción (Anticipado)
74
Fase
- Fase 1
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Shanghai
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Shanghai, Shanghai, Porcelana, 200120
- Reclutamiento
- Shanghai Oriental Hospital
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Contacto:
- Jin Li, Doctor
- Número de teléfono: 86-21-38804518
- Correo electrónico: lijin@csco.org.cn
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
18 años a 75 años (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- Understands and provides written informed consent and willing to follow the requirements specified in protocol;
- Both genders;
- Aged 18 to 75 (including 18 and 75);
- Expected survival time ≥ 12 weeks;
- Patients with histologically and/or cytologically confirmed HER2-positive solid tumors who have failed standard therapy or for whom no standard therapy exists or for whom standard therapy is not appropriate at current stage;
- Patients must have at least one evaluable lesion (Phase Ia) or measurable lesion (Phase Ib) according to the Response Evaluation Criteria in Solid Tumors (RECIST 1.1);
- The score of ECOG for performance status is 0 or 1;
- Prior anti-tumor treatment-related AEs (NCI CTCAE v5.0 Criteria) have recovered to ≤ Grade 1 (except alopecia);
- No severe cardiac dysfunction with left ventricular ejection fraction (LVEF) ≥ 50%;
- Organ functions must meet the basic requirements;
- Coagulation function must meet the basic requirements;
- Cumulative anthracycline dose ≤ 360 mg/m2 doxorubicin or its equivalent, 720 mg/m2 epirubicin.
Exclusion Criteria:
- Received radiotherapy, chemotherapy, biotherapy, immunotherapy, or other anti-tumor drugs within 3 weeks prior to the first dose of MRG002 treatment;
- History of severe cardiac disease;
- Clinically significant abnormalities in rhythm, conduction, and resting ECG morphology;
- Patients with poorly controlled hypertension or clinically significant vascular disease;
- History of moderate to severe dyspnea at rest due to advanced cancer or their complications, severe primary lung disease, or current need of continuous oxygen therapy, or any history of interstitial lung disease (ILD) or pneumonitis;
- Nausea and vomiting of any kind difficult to control, or chronic gastrointestinal disease;
- Patients with symptoms of central nervous system or brain metastasis or received treatment for central nervous system or brain metastasis within 3 months prior to the first dose of MRG002 treatment;
- Major surgery not fully recovery within 4 months prior to the first dose of MRG002 treatment;
- History of hypersensitivity to any component of MRG002 or history of hypersensitivity of ≥ Grade 3 to trastuzumab injection;
- Evidence of active infection of hepatitis B or hepatitis C;
- History of immunodeficiency, including human immunodeficiency virus (HIV) infection, or other immunodeficiency disease, or history of organ transplantation;
- Any serious and/or uncontrolled disease or other condition that, considered by the investigator and sponsor, may compromise the patient's participation in this study;
- Received systemic corticosteroids within 4 weeks prior to the first dose of MRG002 treatment;
- Female patients with a positive serum pregnancy test or who are breast-feeding or who do not agree to take adequate contraceptive measures during the treatment and for 6 months after the last dose of study treatment.
- Other conditions inappropriate for participation in this clinical trial, at the discretion of the investigator.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: MRG002
All patients in Phase Ia (dose escalation) and Phase Ib (dose expansion) will be administrated MRG002 on Day 1 of every 3 weeks (21-day cycle).
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Administrado por vía intravenosa
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Maximum Tolerated Dose (MTD)
Periodo de tiempo: DLT will be evaluated during the first treatment cycle (Day 1-28)
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The highest dose confirmed wherein ≤ 1/6 of patients in a treatment cohort experiences a dose-limiting toxicity (DLT).
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DLT will be evaluated during the first treatment cycle (Day 1-28)
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Recommended Phase II Dose (RP2D)
Periodo de tiempo: Baseline to study completion (up to 6 months)
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The dose level of MRG002 recommended for further clinical studies based on assessment of the safety, efficacy and PK data from this study.
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Baseline to study completion (up to 6 months)
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Adverse Events (AEs)
Periodo de tiempo: Baseline to 49 days after the last dose of study treatment
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Any reaction, side effect, or untoward event that occurs during the course of the clinical trial whether or not the event is considered related to the study drug.
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Baseline to 49 days after the last dose of study treatment
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Objective Response Rate (ORR)
Periodo de tiempo: Baseline to study completion (up to 6 months)
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ORR is defined as the proportion of subjects with CR and PR assessed by IRC and investigator according to RECIST v1.1.
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Baseline to study completion (up to 6 months)
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Duration of Response (DoR)
Periodo de tiempo: Baseline to study completion (up to 6 months)
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DoR is defined as the duration from the initial recording of objective disease response to the first onset of tumor progression, or death of any cause.
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Baseline to study completion (up to 6 months)
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Progression Free Survival (PFS)
Periodo de tiempo: Baseline to study completion (up to 6 months)
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PFS is defined as the duration from the start of treatment to the onset of tumor progression or death of any cause.
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Baseline to study completion (up to 6 months)
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Pharmacokinetics (PK) parameter of MRG002: Cmax
Periodo de tiempo: Baseline to 21 days after the last dose of study treatment
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Maximum observed plasma concentration.
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Baseline to 21 days after the last dose of study treatment
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Pharmacokinetics (PK) parameter of MRG002: Tmax
Periodo de tiempo: Baseline to 21 days after the last dose of study treatment
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Time to reach maximum plasma concentration.
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Baseline to 21 days after the last dose of study treatment
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Pharmacokinetics (PK) parameter of MRG002: t1/2
Periodo de tiempo: Baseline to 21 days after the last dose of study treatment
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The time required for plasma concentration to decreased by on half.
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Baseline to 21 days after the last dose of study treatment
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Pharmacokinetics (PK) parameter of MRG002: AUClast
Periodo de tiempo: Baseline to 21 days after the last dose of study treatment
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Area under the curve up to the last validated measurable plasma concentration.
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Baseline to 21 days after the last dose of study treatment
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Immunogenicity
Periodo de tiempo: Baseline to 21 days after the last dose of study treatment
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The proportion of patients with positive ADA immunogenicity results.
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Baseline to 21 days after the last dose of study treatment
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Jin Li, Doctor, Shanghai Oriental Hospital
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
21 de noviembre de 2018
Finalización primaria (Anticipado)
1 de octubre de 2022
Finalización del estudio (Anticipado)
1 de octubre de 2022
Fechas de registro del estudio
Enviado por primera vez
20 de junio de 2021
Primero enviado que cumplió con los criterios de control de calidad
20 de junio de 2021
Publicado por primera vez (Actual)
28 de junio de 2021
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
3 de diciembre de 2021
Última actualización enviada que cumplió con los criterios de control de calidad
2 de diciembre de 2021
Última verificación
1 de diciembre de 2021
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- MRG002-001
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
No
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
producto fabricado y exportado desde los EE. UU.
No
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