- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07594067
TCR1188-ABC Cells in KRAS-mutated Cancers
Phase I, Open-Label Study of Autologous Mutant KRAS and ILT4-Redirected T-cell Receptor Cells (TCR1188-ABC)
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Abramson Cancer Center Clinical Trials Service
- Número de teléfono: 215-349-8245
- Correo electrónico: PMCancerResearch@pennmedicine.upenn.edu
Ubicaciones de estudio
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-
Pennsylvania
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Philadelphia, Pennsylvania, Estados Unidos, 19104
- Reclutamiento
- University of Pennsylvania
-
Contacto:
- Abramson Cancer Center Clinical Trials Service
- Número de teléfono: 215-349-8245
- Correo electrónico: PMCancerResearch@pennmedicine.upenn.edu
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Patients ≥ 18 years of age
Patients with one of the following diagnoses:
- Histologically confirmed metastatic pancreatic adenocarcinoma or cholangiocarcinoma
- Histologically confirmed metastatic colorectal cancer
- Histologically confirmed metastatic non-small cell lung cancer
- HLA-A*11:01 positive as confirmed by a CLIA certified laboratory.
- KRAS G12V mutation positive disease as confirmed on tissue, blood, or plasma by next generation sequencing by a CLIA certified laboratory.
Received prior treatment for their primary malignancy as follows:
- Pancreatic Cancer/Cholangiocarcinoma Patients: At least one prior line of standard of care therapy for advanced stage disease. For pancreatic cancer patients, this must include a gemcitabine or fluorouracil (5 FU)-based regimen.
- Colorectal Cancer Patients: At least three prior lines of standard of care therapy for advanced stage disease. Prior treatment must include all of the following unless the patient was ineligible for a specific therapy type: i). a fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy regimen, ii). an anti-vascular endothelial growth factor (VEGF) agent, and iii). regorafenib, trifluridine-tipiracil, or fruquintinib. Patients with microsatellite instability-high (MSI-H) disease must also have received, or be ineligible for, prior treatment with an immune checkpoint inhibitor.
- Non-Small Cell Lung Cancer Patients: At least one prior line of standard of care therapy for advanced stage disease.
- Evidence of radiographically detectable disease within 8 weeks of physician-investigator confirmation of eligibility.
Adequate organ function within 4 weeks of eligibility confirmation by a physician-investigator defined as:
- Serum creatinine ≤ 1.5 mg/dl or creatinine clearance ≥ 50 cc/min per the Cockcroft-Gault Equation; Patient must not be on dialysis.
- ALT/AST ≤ 5 x ULN (patients with liver metastases) or ALT/AST ≤ 2.5 x ULN (patients without liver metastases)
- Total bilirubin ≤ 1.5 mg/dL x ULN, unless the subject has Gilbert's syndrome (if so, direct bilirubin must be ≤ 2.0 mg/dL x ULN)
- Left Ventricle Ejection Fraction (LVEF) ≥ 50% confirmed by ECHO/MUGA
- Must have a minimum level of pulmonary reserve defined as ≤ Grade 1 dyspnea and pulse oxygen > 92% on room air
Patients must have adequate hematologic reserve within 4 weeks of eligibility confirmation by a physician-investigator and must not be dependent on transfusions to maintain these hematologic parameters. Adequate hematologic reserve is defined as:
- Hemoglobin ≥ 8 g/dL
- Absolute neutrophil count ≥ 1000/μL
- Platelet count ≥ 100,000/μL
- ECOG Performance Status that is either 0 or 1.
- Signed, written informed consent
Exclusion Criteria:
- Active hepatitis B or hepatitis C infection
- Patients with a severe acquired or inherited immunodeficiency, including HIV positive patients with a CD4 count ≤ 350 cells/μL. In order to qualify, HIV positive patients must also be on an established antiretroviral therapy regimen with a viral load of <400 copies/mL.
- Any other active, uncontrolled infection.
- Class III/IV cardiovascular disability according to the New York Heart Association Classification (see Appendix 5).
- Severe, active co-morbidity that in the opinion of the physician-investigator would preclude participation in the study.
- Active invasive cancer, other than the proposed cancer included in the study, within 2 years prior to eligibility confirmation by a physician-investigator. [Note: non-invasive cancers treated with curative intent (e.g., non-melanoma skin cancer) may still be eligible].
- Pregnant or nursing (lactating) patients. Participants of reproductive potential must agree to use acceptable birth control methods, as described in protocol Section 4.3.
- Patients requiring chronic treatment with systemic steroids or immunosuppressant medications. Low-dose physiologic replacement therapy with corticosteroids equivalent to prednisone 10 mg/day or lower, topical steroids and inhaled steroids are acceptable. For additional details regarding use of steroid and immunosuppressant medications, please see Section 5.6.
- Active autoimmune disease requiring systemic immunosuppressive treatment equivalent to ≥ 10mg daily of prednisone. Patients with autoimmune neurologic diseases (such as MS) will be excluded.
- Patients with unstable angina, serious uncontrolled cardiac arrhythmia, and/or myocardial infarction within 6 months of physician-investigator confirmation of eligibility.
- Prior history of myocarditis.
- Patients with pneumonitis/interstitial lung disease requiring steroid treatment.
- Patients with active/untreated brain metastases. [Note: History of treated metastases may still be eligible.]
- History of allergy or hypersensitivity to study product excipients (human serum albumin, DMSO, and Dextran 40) or tocilizumab.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Dose level -1
1.11 x 10^8 TCR1188-ABC cells
|
TCR1188 modified, base-edited autologous CD4+ and CD8+ T cells expressing TCR1188 and a scFv fragment specific to ILT4 (LILRB2) as a Single infusion on Day 0
Fludarabine: 30 mg/m2/day x 4 days (Day -7 to -4) Cyclophosphamide: 600mg/m2/day x 3 days (Day -7 to -5)
Single administration of 8mg/kg on Day 2 (+3d)
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|
Experimental: Dose level 1
3.33 x 10^8 TCR1188-ABC cells
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TCR1188 modified, base-edited autologous CD4+ and CD8+ T cells expressing TCR1188 and a scFv fragment specific to ILT4 (LILRB2) as a Single infusion on Day 0
Fludarabine: 30 mg/m2/day x 4 days (Day -7 to -4) Cyclophosphamide: 600mg/m2/day x 3 days (Day -7 to -5)
Single administration of 8mg/kg on Day 2 (+3d)
|
|
Experimental: Dose level 2
1 x 10^9 TCR1188-ABC cells
|
TCR1188 modified, base-edited autologous CD4+ and CD8+ T cells expressing TCR1188 and a scFv fragment specific to ILT4 (LILRB2) as a Single infusion on Day 0
Fludarabine: 30 mg/m2/day x 4 days (Day -7 to -4) Cyclophosphamide: 600mg/m2/day x 3 days (Day -7 to -5)
Single administration of 8mg/kg on Day 2 (+3d)
|
|
Experimental: Dose level 3
3 x 10^9 TCR1188-ABC cells
|
TCR1188 modified, base-edited autologous CD4+ and CD8+ T cells expressing TCR1188 and a scFv fragment specific to ILT4 (LILRB2) as a Single infusion on Day 0
Fludarabine: 30 mg/m2/day x 4 days (Day -7 to -4) Cyclophosphamide: 600mg/m2/day x 3 days (Day -7 to -5)
Single administration of 8mg/kg on Day 2 (+3d)
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of Subjects with treatment related adverse events using NCI Common Terminology Criteria for Adverse Events (CTCAE) V6.0
Periodo de tiempo: Up to 15 years following TCR1188-ABC cell administration
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Type, frequency, severity, and attribution of adverse events
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Up to 15 years following TCR1188-ABC cell administration
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Occurrence of dose-limiting toxicities (DLTs)
Periodo de tiempo: Up to 28 days following TCR1188-ABC cell administration
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Type, frequency, severity, and attribution of dose limiting adverse events as defined by the protocol
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Up to 28 days following TCR1188-ABC cell administration
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|
Identification of the maximum tolerated dose (MTD)
Periodo de tiempo: 28 days post-TCR1188-ABC cell infusion
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The highest dose at which 0 or 1 DLT occurs in 6 DLT-evaluable subjects will be declared the MTD.
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28 days post-TCR1188-ABC cell infusion
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Occurrence of product release failures
Periodo de tiempo: 3 months
|
Calculated based on the proportion of subjects with TCR1188-ABC cell products that fail to meet the product release criteria, out of the number of eligible subjects in whom manufacturing was attempted, will be calculated.
|
3 months
|
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Proportion of TCR1188-ABC cells that fail to meet the protocol-defined dose
Periodo de tiempo: 3 months
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Proportion of subjects with TCR1188-ABC cell products that fail to meet the assigned dose, out of the number of eligible subjects in whom manufacturing was attempted.
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3 months
|
|
Overall Response Rate (ORR)
Periodo de tiempo: Up to 12 months following TCR1188-ABC cells administration
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Proportion of subjects with CR or PR as the best overall response as assessed by RECIST 1.1 from the first response assessment post-infusion until the end of the primary follow-up.
|
Up to 12 months following TCR1188-ABC cells administration
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Duration of Response (DOR)
Periodo de tiempo: Up to 15 years following TCR1188-ABC cell administration
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Duration of time from the date the response criteria of CR or PR is first met, to the date of confirmed disease progression, or the date of the last adequate disease assessment performed before the occurrence of another censoring event.
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Up to 15 years following TCR1188-ABC cell administration
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|
Progression-Free Survival (PFS)
Periodo de tiempo: Up to 15 years following TCR1188-ABC cell administration
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Duration of time from the TCR1188-ABC cell infusion to the date of confirmed disease progression or death due to any cause, or the date of the last adequate disease assessment performed before the occurrence of another censoring event.
|
Up to 15 years following TCR1188-ABC cell administration
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Overall Survival (OS)
Periodo de tiempo: Up to 15 years after last TCR1188-ABC cells administration
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Time from the first TCR1188-ABC cell infusion to death due to any cause; or censored at the date of last contact.
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Up to 15 years after last TCR1188-ABC cells administration
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Neoplasias por sitio
- Neoplasias
- Enfermedades intestinales
- Enfermedades de las vías respiratorias
- Neoplasias por tipo histológico
- Neoplasias Gastrointestinales
- Neoplasias del Sistema Digestivo
- Enfermedades del Sistema Digestivo
- Enfermedades Gastrointestinales
- Neoplasias Intestinales
- Enfermedades Rectales
- Enfermedades pulmonares
- Neoplasias Glandulares y Epiteliales
- Adenocarcinoma
- Neoplasias de las vías respiratorias
- Neoplasias torácicas
- Enfermedades del Colon
- Neoplasias Pulmonares
- Carcinoma
- Carcinoma Broncogénico
- Neoplasias Bronquiales
- Neoplasias colorrectales
- Carcinoma de pulmón de células no pequeñas
- Colangiocarcinoma
- tocilizumab
- fludarabina
Otros números de identificación del estudio
- 27225
- 1UG3CA283652-01 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .