A Study of NT-112 in HLA-C*08:02-Positive Adult Subjects With Unresectable, Advanced, and/ or Metastatic Solid Tumors Positive for the KRAS G12D Mutation

Estado del programa

Activo, no recluta

Fase

Fase 1

Inmunoterapia previa permitida

Ensayo dirigido por el CRC

Etiquetas

MSI-H/ MMRd, MSS/ MMRp

Comentarios

Adoptive cells immunotherapy, targeted to KRAS G12D mutation.
Admits patients with Stage III or IV colon and/or rectal cancer, with KRAS G12D mutation and  HLA-C*08:02 positive (both, MSS and MSI-H)

NT-112: Autologous, engineered T Cells targeting KRAS G12D
At least 1 line of prior treatment required, not prior adoptive cell and gene therapy allowed (not mention of prior checkpoint inhibitor being an exclusion criterion).

Patients receive a with fludarabine and cyclophosphamide, and late one unique infusion of T cell receptor (TCR) T cells. After that, other immunotherapy, recombinant interleukin-2 (rIL-2).

Ubicación Situación
Estados Unidos
Research Site
Duarte, California 91010
Activo, no recluta
Research Site
Los Ángeles, California 90095
Activo, no recluta
Research Site
Newport Beach, California 92663
Activo, no recluta
Research Site
Westwood, Kansas 66205
Activo, no recluta
Research Site
San Luis, Missouri 63110
Activo, no recluta
Research Site
Nueva York, Nueva York 10016
Activo, no recluta
Research Site
Pittsburgh, Pennsylvania 15237
Activo, no recluta
Research Site
Nashville, Tennessee 37203
Activo, no recluta
Research Site
Dallas, Texas 75246
Activo, no recluta
Research Site
Galveston, Texas 77555
Activo, no recluta
Research Site
Houston, Texas 77030
Activo, no recluta
Research Site
Aberdeen, Washington 98520
Activo, no recluta
Research Site
Milwaukee, Wisconsin 53226
Activo, no recluta

Criterios de inclusión

Key Inclusion Criteria:

* Age ≥18 years
* Diagnosed with NSCLC, Colorectal adenocarcinoma, Pancreatic adenocarcinoma, Endometrial Cancer or any other solid tumor
* Tumors must harbor a KRAS G12D variant mutation and subject must be HLA-C*08:02 positive
* Subject has advanced solid cancer, defined as unresectable, advanced, and/or metastatic disease (Stage III or IV) after at least 1 line of approved systemic standard of care (SOC) treatment regimen and for which there are no available curative treatment options.
* Presence of at least 1 measurable lesion per RECIST v1.1
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 at the time of enrollment

Key

Criterios de exclusión

Criterios de exclusión:

* Any other primary malignancy within the 3 years prior to enrollment (except for non-melanoma skin cancer, carcinoma in situ (eg, cervix, bladder, breast) or low-grade prostate cancer
* Known, active primary central nervous system (CNS) malignancy
* History of prior adoptive cell and gene therapy, allogeneic stem cell transplant or solid organ transplantation.
* History of stroke or transient ischemic attack within the 12 months prior to enrollment.
* History of clinically significant cardiac disease within the 6 months prior to enrollment or heart failure at any time prior to enrollment.
* Systemic therapy within at least 2 weeks or 3 half-lives, whichever is shorter, prior to enrollment.
* Any form of primary immunodeficiency.
* Active immune-mediated disease requiring systemic steroids or other immunosuppressive treatment (except if related to prior checkpoint inhibitor therapy)
* Female of childbearing potential who is lactating or breast feeding at the time of enrollment

NCT ID

NCT06218914

Fecha en que se añadió el juicio

2024-01-23

Fecha de actualización

2025-04-27