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KXV01 Injection in Patients With Advanced Solid Tumor (Including Osteosarcoma and Sarcoma)

13 de mayo de 2026 actualizado por: TCRx Therapeutics Co.Ltd

A Phase I Clinical Study on the Safety, Tolerability, and Efficacy of KXV01 Injection in Patients With Advanced Solid Tumor (Including Osteosarcoma and Sarcoma)

This is a single center, single arm, open-label, dose escalation, phase 1 study to evaluate the safety, tolerability and preliminary efficacy of KXV01 TCR Lentinvivo for patients with advanced solid tumors.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

In recent years, the field has found that patient-specific anti-tumor treatment technologies have increasingly significant clinical application prospects and clinical value. Patient-specific anti-tumor in vivo TCR gene therapy is an advanced therapeutic strategy that can specifically recognize tumor neoantigens. This strategy is not restricted by patients' HLA typing nor by the type of indication.

This investigator-initiated clinical study aims to evaluate KXV01 TCR Lentinvivo, the third-generation self-inactivating lentiviral vector that carries patient-derived personalized tumor reactive TCR, in patients with advanced solid tumors. The study employs a BOIN design to assess safety, tolerability, and preliminary efficacy.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

30

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: Weichi Zhou
  • Número de teléfono: +86-18994103369
  • Correo electrónico: zhouwc@tcrximmune.cn

Ubicaciones de estudio

      • Shanghai, Porcelana, 200233
        • Reclutamiento
        • Shanghai Sixth People's Hospital Affiliated to Shanghai JiaoTong University
        • Contacto:

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

Screening Period 1

Inclusion Criteria 1:

  1. Voluntarily participate in the clinical study; fully understand the study and voluntarily sign the informed consent form; be willing to comply with and able to complete all trial procedures.
  2. Aged 18 to 70 years (inclusive).
  3. Histologically or cytologically confirmed incurable or metastatic solid tumors that have failed standard treatment, or for which no standard treatment is currently available.
  4. Expected survival time > 6 months.
  5. ECOG performance status of 0 or 1.
  6. Sufficient organ function.
  7. Patients whose tumor lesions can be collected and from whom tumor-reactive TCR sequences can be identified may enter the study.
  8. Women of childbearing age must have a negative urine/blood pregnancy test during the screening period and agree to use contraceptive measures for at least 1 year after administration; male subjects whose partners are of childbearing potential must agree to use effective barrier contraception for at least 1 year after administration.

Exclusion Criteria 1:

  1. A history of other malignant tumors within 2 years prior to signing the informed consent form, except for non-melanoma skin cancer, some in situ carcinomas (e.g., cervical cancer, bladder cancer, breast cancer), or low-risk prostate cancer.
  2. Uncontrolled infectious diseases within 4 weeks prior to signing the informed consent form.
  3. Active hepatitis B or hepatitis C virus infection.
  4. Patients with HIV infection.
  5. Patients with positive Treponema pallidum.
  6. A history of any of the following cardiovascular diseases within the past 6 months: New York Heart Association (NYHA) Class III or IV heart failure, coronary angioplasty or stenting, myocardial infarction, unstable angina, or other clinically significant heart diseases.
  7. Tumor lesions invading the heart or major blood vessels.
  8. Abnormal pulmonary function indicated by a ratio of forced expiratory volume in 1 second (FEV1) to forced vital capacity (FVC) < 70% in pulmonary function tests.
  9. A history of clinically significant central nervous system (CNS) disorders, including but not limited to epilepsy, paresis, aphasia, stroke, severe traumatic brain injury, dementia, Parkinson's disease, cerebellar disease, and organic brain syndrome.
  10. Females who are pregnant or breastfeeding.
  11. A history of primary immunodeficiency or autoimmune disease.
  12. Patients whose disease or condition renders them unable to understand, participate in, and/or comply with the study protocol.
  13. Any other disease that the investigator believes would impair the subject's ability to tolerate protocol treatment or significantly increase the risk of complications.
  14. Current or past history of psychoactive substance abuse or dependence.
  15. Subjects whose underlying condition, in the investigator's judgment, may increase the risk of receiving the investigatory drug or confound the interpretation of toxic reactions and adverse events.
  16. Other conditions deemed unsuitable for participation in the study by the investigator.

Screening Period 2

Inclusion Criteria 2:

The patient's organ function and key test items at this stage should not have significant changes compared with their test results in Screening Period 1. If the patient's test results in Screening Period 2 exceed the following criteria, they should not receive administration of KXV01 Injection until the abnormal items return to the normal range.

  1. The patient's KXV01 Injection has been successfully prepared.
  2. Expected survival time > 6 months.
  3. ECOG performance status of 0 or 1.
  4. Sufficient organ function.
  5. Females of childbearing potential have a negative blood pregnancy test within 7 days prior to administration of the study drug (Non-childbearing potential: surgically sterilized or postmenopausal for at least 2 years). In addition, female subjects of childbearing potential must use medically approved contraceptive measures for 12 months after the start of study treatment and have no egg retrieval during this period.
  6. Male subjects are willing to use medically approved contraceptive measures from the time of signing the informed consent form until 12 months after the start of study treatment, and will not donate sperm during this period.
  7. At least one measurable lesion according to RECIST v1.1 criteria.
  8. Toxicities and adverse reactions caused by prior therapy should have resolved to Grade ≤ 1 (except for toxicities considered clinically insignificant, such as chemotherapy-induced alopecia).

Exclusion Criteria 2:

  1. Prior to administration of the study drug, the subject's anti-tumor therapy has not been sufficiently washed out (2 weeks or 5 half-lives, whichever is shorter).
  2. Uncontrolled infectious diseases within the previous 4 weeks.
  3. Active hepatitis B or hepatitis C virus infection.
  4. Patients with HIV infection.
  5. Patients with positive Treponema pallidum.
  6. Tumor lesions invading the heart or major blood vessels.
  7. A history of clinically significant central nervous system (CNS) disorders, including but not limited to epilepsy, paresis, aphasia, stroke, severe traumatic brain injury, dementia, Parkinson's disease, cerebellar disease, and organic brain syndrome.
  8. Known primary central nervous system (CNS) malignancy or symptomatic CNS metastases.
  9. Use of the restricted drugs or treatments between Screening Period 1 and Screening Period 2 per the protocol.
  10. Females who are pregnant or breastfeeding.
  11. Subjects whose underlying condition, in the investigator's judgment, may increase the risk of receiving the investigatory drug or confound the interpretation of toxic reactions and adverse events.
  12. Receipt of major surgery (excluding diagnostic surgery) between Screening Period 1 and Screening Period 2, or expected to undergo major surgery during the study period. Subjects with planned or ongoing minor surgical procedures (such as venous access placement, etc.) are eligible for enrollment.

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
Experimental: Inyección de KXV01 TCR Lentinvivo
KXV01 TCR Lentinvivo Inyección
La inyección de lentinvivo de KXV01 TCR es un tipo de vector de lentivirus autoinactivante no replicativo de tercera generación que lleva el TCR reactivo tumoral personalizado de un paciente efectivo.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Toxicidad limitante de la dosis
Periodo de tiempo: 28 días después del administrador
Período de evaluación de DLT: el período de evaluación DLT se define como dentro de los 28 días (inclusive) después de la primera infusión de los sujetos de inyección de KXV01 durante la etapa de escalada de dosis. Todos los eventos adversos deben ser calificados y evaluados de acuerdo con CTCAE v5.0. Entre ellos, el síndrome de liberación de citocinas (CRS) y el síndrome de neurotoxicidad relacionado con las células inmunes (ICAN) deben determinarse y graduarse de acuerdo con los estándares de la Sociedad Americana de Trasplante y Terapia Celular (ASTCT).
28 días después del administrador

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

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)

19 de diciembre de 2025

Finalización primaria (Estimado)

31 de diciembre de 2027

Finalización del estudio (Estimado)

31 de diciembre de 2029

Fechas de registro del estudio

Enviado por primera vez

13 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

13 de mayo de 2026

Publicado por primera vez (Actual)

19 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

19 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

13 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • KXV01-R102

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

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. .

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