- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07613723
A Study to Test the Safety, Tolerability and Effect of ZI-MA4-1 for Patients With Locally Advanced or Metastatic Solid Malignancies
1 de septiembre de 2026 actualizado por: Zelluna Immunotherapy AS
A Phase 1, Dose-Escalation, Open-Label Study, Evaluating the Safety and Tolerability of ZI-MA4-1, a TCR-NK Cell Therapy, in HLA-A*02:01 Positive Patients With Inoperable, Locally Advanced, or Metastatic MAGE-A4 Expressing Solid Malignancies
This study will recruit patients with the following cancer indications: ovarian cancer, squamous non-small cell lung cancer, synovial sarcoma and head and neck cancer, with inoperable locally advanced or metastatic solid tumours.
Currently, these patients have a poor prognosis and a relatively short overall survival.
There is a lack of meaningful, effective therapies available that improve the outcome for these patients.
The treatment being investigated in this study is ZIMA4-1, an allogeneic cell therapy product.
This is the first time ZI-MA4-1 will be administered to humans.
The study is planned to consist of two parts (A and B).
Part A includes up to four dose escalation cohorts and aims to identify the maximum tolerated dose of ZI-MA4-1 and give insight into the recommended Phase 2 dose (RP2D).
Part B consists of an expansion cohort and is designed to further evaluate the RP2D identified in Part A across one or more indications.
The study procedures and eligibility criteria will be the same for participants in Parts A and B, except for the dose level of ZI-MA4-1.
Descripción general del estudio
Estado
Reclutamiento
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
9
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.
Estudio Contacto
- Nombre: Zelluna Immunotherapy
- Número de teléfono: +47 413 80 080
- Correo electrónico: ctinfo@zelluna.com
Ubicaciones de estudio
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London, Reino Unido
- Reclutamiento
- The Royal Marsden NHS Foundation Trust
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Contacto:
- Dr. Furness
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Manchester, Reino Unido
- Reclutamiento
- The Christie NHS Foundation Trust
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Contacto:
- Prof. Thistlethwaite
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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
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- HLA-A*02:01 positive
- Tumour(s) show expression of the MAGE-A4 protein above a defined threshold
- Histopathological or cytological diagnosis of inoperable Locally Advanced or Metastatic malignant disease: ovarian cancer, squamous non-small cell lung cancer (NSCLC), synovial sarcoma or head and neck cancer.
- No approved therapy with demonstrated clinical benefit is indicated or available to treat the patient, or the patient is intolerant of or has refused standard of care therapy.
- Documented imaging confirmed disease progression while on or within 6 months after the end of the most recent therapy.
- Participant must have received ≥2 prior lines of cancer therapy except for patient with synovial sarcoma for whom ≥1 prior lines of cancer therapy.
- Measurable disease according to RECIST v1.1 criteria.
- ECOG performance status of 0 or 1 with no deterioration over the previous 2 weeks, and an anticipated life expectancy of >3 months
- Female participants are eligible to participate if they are not pregnant or breastfeeding. Woman of childbearing potential must have negative pregnancy test and agree to use an effective contraceptive method.
Other protocol defined inclusion criteria could apply.
Exclusion Criteria:
- Patients have received any prior cellular or gene therapy.
- Receiving experimental investigational products within 4 weeks of lymphodepletion.
- Recent therapies (within up to 4 weeks prior to lymphodepletion) including biologic agents (such as monoclonal antibodies), anti-cancer immunotherapy (such as monoclonal antibodies against PD-1 receptor or ligand).
- Residual toxicities ≥2 CTCAE grade due to prior therapy, that in the opinion of the investigator may interfere with study conduct.
- Any other active malignancy besides the tumour under study within 3 years prior to screening except for in situ removal of basal cell carcinoma or adequately treated cervix carcinoma in-situ.
- Active or documented history of autoimmune disease or any other diseases requiring immunosuppressive therapy or corticosteroid therapy. Physiological replacement, topical, and inhaled steroids are permitted.
- Significant CNS disorders.
- Myocardial infarction, cardiac angioplasty or stenting, cardiac arrhythmia requiring medication, unstable angina, New York Heart Association Class II or greater congestive heart failure, cardiac atrial or ventricular lymphoma involvement, or other clinically significant cardiac disease within 6 months of enrolment.
- Active fungal, bacterial viral, or other infection requiring intravenous antibiotic, antifungal, or antiviral medication within 7 days prior to lymphodepletion.
- Received or planned to receive a live vaccine ≤6 weeks before the planned start date of lymphodepletion.
- Severe or uncontrolled medical condition (e.g., severe chronic obstructive pulmonary disease, interstitial lung disease , severe Parkinson's disease, active inflammatory bowel disease) or psychiatric condition, which in the opinion of the investigator would interfere with study activities.
- Active bleeding diatheses, including but not limited to therapeutic anticoagulation, and treatment with major surgery within 28 days before lymphodepletion (minor surgical procedures such as lymph node biopsy/excision or catheter placement are permitted).
- Patients have significant immunosuppression
- Known significant hepatic or biliary abnormalities. Active infection with hepatitis B, hepatitis C.
- Any medical, psychological, or social condition, drug or alcohol abuse that would make it difficult for the patient to participate in the study and comply with the study procedures, restrictions, and requirements.
- History of allergic reactions to compounds chemically or biologically similar to cyclophosphamide, fludarabine or other agents used in the study
- QTc > 450 msec for male participants or > 470 msec for female participants
- Medical conditions, such as anti-coagulation, which is not suitable for reversal which, at the opinion of the investigator, preclude or make the patient a poor candidate for biopsy.
- Personal history of allergies or intolerance to local anaesthetic.
- Recent treatment with immunosuppressive agents
- Residual toxicities ≥2 Common Terminology Criteria for Adverse Events (CTCAE) grade due to prior therapy, that in the opinion of the investigator may interfere with study conduct Other protocol defined exclusion criteria could apply.
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: ZI-MA4-1 (TCR-NK cells)
Participants receive ZI-MA4-1 administered via IV infusion 3 times per treatment cycle at their assigned dose.
It is planned that all participants in the study will get a minimum of one treatment cycle and up to a maximum of two treatment cycles.
Prior to a treatment cycle, a participant is given fludarabine and cyclophosphamide to temporarily reduce lymphocytes in the body (lymphodepletion).
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Quimioterapia linfodepletora
Quimioterapia linfodepletora
Allogeneic Natural Killer cells transduced with a T cell receptor targeting the tumour-specific melanoma-associated antigen 4 (MAGE-A4)
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Safety and tolerability of ZI-MA4-1
Periodo de tiempo: From baseline through end of study visit (up to 5 years)
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Assessed using clinical assessments and adverse event reporting, including dose-limiting toxicities (DLTs), treatment-emergent adverse events (TEAEs), and treatment-related adverse events (TRAEs)
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From baseline through end of study visit (up to 5 years)
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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MTD and RP2D of ZI-MA4-1
Periodo de tiempo: Through completion of study response follow-up (up to 2 years)
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Identification of maximum tolerated dose (MTD) and the recommended Phase 2 dose (RP2D) of ZI-MA4-1 based on observed DLTs and predefined dose-escalation rules
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Through completion of study response follow-up (up to 2 years)
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Long term safety
Periodo de tiempo: Through end of study visit (up to 5 years)
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Evaluate ZI-MA4-1 for the occurrence of delayed adverse events (AEs)
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Through end of study visit (up to 5 years)
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Minimum biologically active dose (MBAD) of ZI-MA4-1
Periodo de tiempo: Through completion of study response follow-up (up to 2 years)
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Assessment of preliminary anti-tumour activity
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Through completion of study response follow-up (up to 2 years)
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Objective Response Rate (ORR)
Periodo de tiempo: Through completion of study response follow-up (up to 2 years)
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Assessed by RECIST 1.1
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Through completion of study response follow-up (up to 2 years)
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Best Overall Response (BOR)
Periodo de tiempo: Through completion of study response follow-up (up to 2 years)
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Assessed by RECIST 1.1
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Through completion of study response follow-up (up to 2 years)
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Disease Control Rate (DCR)
Periodo de tiempo: Through completion of study response follow-up (up to 2 years)
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Assessed by RECIST 1.1
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Through completion of study response follow-up (up to 2 years)
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Pharmacokinetics of ZI-MA4-1
Periodo de tiempo: 3 years post-infusion of ZI-MA4-1
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Evaluation of persistence of ZI-MA4-1 cells in the blood using vector copy number (VCN) analysis
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3 years post-infusion of ZI-MA4-1
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
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)
11 de mayo de 2026
Finalización primaria (Estimado)
1 de diciembre de 2028
Finalización del estudio (Estimado)
1 de diciembre de 2032
Fechas de registro del estudio
Enviado por primera vez
15 de mayo de 2026
Primero enviado que cumplió con los criterios de control de calidad
21 de mayo de 2026
Publicado por primera vez (Actual)
29 de mayo de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
4 de septiembre de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
1 de septiembre de 2026
Última verificación
1 de septiembre de 2026
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades urogenitales
- Enfermedades Genitales
- Enfermedades del sistema endocrino
- Neoplasias urogenitales
- Neoplasias por sitio
- Neoplasias
- Enfermedades urogenitales femeninas
- Enfermedades urogenitales femeninas y complicaciones del embarazo
- Neoplasias por tipo histológico
- Enfermedades Genitales Femeninas
- Neoplasias de glándulas endocrinas
- Enfermedades Ováricas
- Enfermedades anexiales
- Neoplasias Genitales Femeninas
- Trastornos gonadales
- Sarcoma
- Neoplasias De Tejidos Conectivos Y Blandos
- Neoplasias Del Tejido Conectivo
- Neoplasias Ováricas
- Neoplasias de Cabeza y Cuello
- Sarcoma Sinovial
- Químicos orgánicos
- Hidrocarburos
- Mostaza de fosforamida
- Compuestos de mostaza de nitrógeno
- Compuestos de mostaza
- Hidrocarburos, halogenados
- Fosforamidas
- Compuestos organofosforados
- Ciclofosfamida
- fludarabina
Otros números de identificación del estudio
- ZIMA-101
- ISRCTN14753723 (Identificador de registro: ISRCTN registry)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
INDECISO
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
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