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Phase 1/2 Study of Intravenous Injection of STX-003 in Advanced Solid Tumors as Monotherapy or in Combination With Pembrolizumab

3 de agosto de 2026 actualizado por: Strand Therapeutics Inc.

A Phase 1/2, Open-label, Multi-center, First-in-human Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Antitumor Activity of STX-003 Delivered Intravenously in Patients With Advanced Solid Tumors as a Monotherapy or in Combination With Pembrolizumab

Phase 1/2, Open-label, Multi-center, First-in-human Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Anti-tumor Activity of STX-003 Delivered by Intravenous Injection in Patients with Advanced Solid Tumors as a Monotherapy or in Combination with Pembrolizumab.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

This open-label, Phase 1/2, first-in-human (FIH), multiple ascending dose and dose expansion study involves STX-003 administration, alone or in combination with pembrolizumab, to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity in patients with advanced cancers. (Update after review)

Tipo de estudio

Intervencionista

Inscripción (Estimado)

220

Fase

  • Fase 2
  • 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: Jason Luke, MD, Chief Medical Officer
  • Número de teléfono: 617-993-9271
  • Correo electrónico: stx-003-study@strandtx.com

Ubicaciones de estudio

    • Arizona
      • Scottsdale, Arizona, Estados Unidos, 85258
        • Reclutamiento
        • HonorHealth Research Institute
        • Investigador principal:
          • Justin Moser, MD
        • Contacto:
    • Tennessee
      • Nashville, Tennessee, Estados Unidos, 37203
        • Reclutamiento
        • Sarah Cannon Research Institute
        • Investigador principal:
          • Melissa Johnson, MD
        • 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

Inclusion Criteria:

  • Inclusion Criteria (Phase 1 and Phase 2)

    1. Mentally competent and able to understand and sign the ICF.
    2. Tumor type for which there is an FDA-approved anti-PD-1/L1 antibody therapy, specifically including biomarker labeled subsets (i.e. PD-L1+) as well as anatomical subsets in some disease (cutaneous melanoma is eligible whereas acral, mucosal and uveal are not; Phase 1) and advanced cutaneous melanoma or PD-L1+ NSCLC.
    3. Histologically or cytologically documented, locally advanced, or metastatic solid tumor.
    4. At least one measurable lesion per RECIST v1.1 criteria.
    5. The patient lacks a curative therapy or has progressive disease despite, or refused, standard therapy.
    6. ECOG performance status of 0 or 1.
    7. Life expectancy of ≥ 12 weeks per the Investigator.
    8. ≥ 18 years of age at the time of informed consent.
    9. Body weight ≥ 40 kg.
    10. WOCBP and males with female partners of child-bearing potential must agree to use adequate birth control throughout their participation and for 3 months following the last dose of STX-003.
    11. Willing and able to comply with protocol required assessments.

Hematology:

  • ANC ≥ 1,000 cells/mm3.
  • Platelet count ≥ 75,000 cells/mm3.
  • Hemoglobin ≥ 8.0 g/dL.

    • Renal: Serum creatinine < 1.5 × ULN or creatinine clearance ≥ 40 mL/min based on the Cockcroft-Gault glomerular filtration rate estimation

Coagulation:

  • PT/INR or PT must be ≤ 1.5 × ULN.
  • aPTT ≤ 1.5 × ULN unless undergoing anticoagulation therapy.

    • Liver:

  • Albumin ≥ 3.5 g/dL or within the normal range of the local reference laboratory.
  • AST and ALT < 2 × ULN.
  • Bilirubin ≤ 1.5 × ULN (except participants with documented Gilbert's syndrome who may be enrolled if the conjugated bilirubin is within normal limits) or ≤ 5 × ULN with liver metastases.

Phase 2 Inclusion Criteria

13. NSCLC :

  • Histologically or cytologically documented findings consistent with NSCLC not amenable to curative surgery, radiation, or other therapy.
  • Biomarker confirmed as PD-L1+ per local institutional standard practice.
  • Patients with known activating EGFR, STK11 or KEAP1 mutations as well as ALK/ROS1 fusions, are not eligible.
  • Prior treatment (for advanced, metastatic or [neo]adjuvant) should have included a platinum-based therapy and a PD-1/L1 pathway checkpoint inhibitor, unless the patient is not a candidate for or has refused viable therapies due to inability to tolerate treatment (i.e. cell therapy) or potential side effects (i.e. checkpoint inhibitor toxicity).

    14. Melanoma : Histologically or cytologically documented findings consistent with advanced cutaneous melanoma not amenable to curative surgery, radiation, or other therapy. Acral, mucosal and uveal melanoma are excluded.

  • Patients who are not candidates for or have refused available therapies due to inability to tolerate treatment (i.e. cell therapy) or potential side effects (i.e. checkpoint inhibitor toxicity) are also eligible.
  • Received an anti-PD-1/PD-L1 inhibitor as monotherapy or in combination with anti-CTLA-4 inhibitor and have either primary or secondary checkpoint inhibitor resistance asper SITC consensus definition, unless deemed intolerable by the Investigator. Patients with BRAF V600E mutant melanoma should have received a BRAF inhibitor as monotherapy or in combination with other targeted agents (MAPK kinase MEK inhibitors), unless deemed intolerable by the Investigator.

Exclusion Criteria:

  • Exclusion Criteria (Phase 1 and 2)

    1. Medical Conditions

      • History of primary immune deficiency.
      • History of clinically significant autoimmune disease that has required intervention in the last 6 months. Consultation with the MM may inform the discussion of whether autoimmune disease is clinically significant.
      • History of Grade 3 or higher IRAEs that has not resolved to Grade ≤ 1 at the time of enrollment. Exceptions include endocrine disorders that are well-managed with stable physiological hormone replacement and Grade 3 immune-related rash. Patients meeting this criterion may be considered for enrollment following approval by the MM.
      • History of solid organ transplant and taking immunosuppressive medications.
    2. Cardiovascular exclusions

      • Medical history of an arterial thrombotic event, stroke, or transient ischemic attack within the past 6 months.
      • Medical history of symptomatic congestive heart failure (New York Heart Association classes II-IV) or a cardiac arrhythmia that required treatment within the past 6 months.
      • Medical history of myocardial infarction or unstable angina within 6 months before C1D1.
    3. Recent medical concerns exclusions

      • Evidence of active infection requiring IV antibiotics within 7 days prior to C1D1.
      • Active uncontrolled bleeding, or a bleeding diathesis within 7 days prior to C1D1.
      • Serious or non-healing wound, fistula, skin ulcer, or non-healing bone fracture within 7 days prior to C1D1.
      • Known HIV infection, active hepatitis B infection, or hepatitis C infection:
  • Virology evaluation should be conducted at Screening to include serum HIV antibody, HBc antibody, HBsAg antigen, and HCV antibody. Patients with a positive antibody evaluation for HCV and/or HBc should undergo evaluation to measure HCV RNA or HBV DNA, respectively.

    • Untreated CNS tumor, epidural tumor or metastasis, or brain metastasis. Patients with any primary CNS malignancy including glioma and current, active, or progressing CNS malignancy, including carcinomatosis meningitis, are excluded.
    • Patients with treated brain metastases are eligible if there is no evidence of progression for at least 4 weeks after CNS-directed treatment, as ascertained by clinical examination and brain imaging (MRI or CT scan) during the Screening period and are off systemic steroids (for at least 2 weeks prior to first dose).
    • Another primary malignancy that has not been treated with curative intent (discuss with MM), except for non-metastatic cutaneous basal cell or squamous cell carcinoma, or non-muscle invasive bladder cancer.
    • Serious illness considered by the Investigator as incompatible with participating in this clinical study.
    • Major surgery within 4 weeks of first dose of study drug.
    • Any condition that, in the opinion of the Investigator, would interfere with evaluation of the investigational product or interpretation of the patients' safety or study results.

      4. Prior/Concomitant Therapy

    • Prior treatment with STX-003 or other VEEV-based replicating RNA.
    • Prior IL-12 therapy.
    • Receipt of any live vaccine within 30 days prior to the first dose of study treatment.
    • Use of another systemic anticancer therapy within 3 weeks prior to C1D1 or 5 halflives, whichever is shorter or use of radiotherapy within 1 week prior to C1D1 5. Prior/Concurrent Clinical Study Experience
    • Previously enrolled in this study.
    • Actively enrolled in another clinical study unless it is an observational (noninterventional) clinical study or the follow-up component of an interventional study.
    • Known severe hypersensitivity (Grade ≥ 3) to study treatment or any of the excipients of the products.

Other Exclusions

  • History of interstitial lung disease or active, non-infectious pneumonitis (combination cohorts only).
  • Known psychiatric or substance use disorder that would interfere with the patient's ability to cooperate with the requirements of the study.
  • Currently pregnant (confirmed with a positive pregnancy test), breast-feeding or planning to become pregnant within 6 months following treatment. For WOCBP, a negative serum β-HCG result must be available within a 72-hour window before the first treatment dose.

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: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Phase 1 Monotherapy
STX-003 administered intravenously, at ascending doses across sequential cohorts, once per cycle for up to 35 cycles (approximately 24 months).
STX-003 is a LNP formulated self-replicating mRNA encoding the therapeutic payload human IL-12 (hIL-12) with miRNA target sites to sense specific endogenous miRs.
Experimental: Phase 1 Combination (STX-003 with Pembrolizumab)
STX-003 administered intravenously, at ascending doses across sequential cohorts, once per cycle in combination with pembrolizumab for up to 35 cycles (approximately 24 months).
STX-003 is a LNP formulated self-replicating mRNA encoding the therapeutic payload human IL-12 (hIL-12) with miRNA target sites to sense specific endogenous miRs.
Pembrolizumab (Keytruda USPI 2026) is a marketed PD-1 blocking humanized monoclonal IgG4 kappa antibody.
Experimental: Phase 2 Monotherapy (STX-003)
STX-003 administered intravenously, at 4 planned dose expansion cohorts in patients with advanced cancers with high unmet need, once per cycle for up to 35 cycles (approximately 24 months).
STX-003 is a LNP formulated self-replicating mRNA encoding the therapeutic payload human IL-12 (hIL-12) with miRNA target sites to sense specific endogenous miRs.
Experimental: Phase 2 Combination (STX-003 with Pembrolizumab)
STX-003 administered intravenously, at 4 planned dose expansion cohorts in patients with advanced cancers with high unmet need, once per cycle for up to 35 cycles (approximately 24 months).
STX-003 is a LNP formulated self-replicating mRNA encoding the therapeutic payload human IL-12 (hIL-12) with miRNA target sites to sense specific endogenous miRs.
Pembrolizumab (Keytruda USPI 2026) is a marketed PD-1 blocking humanized monoclonal IgG4 kappa antibody.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence of TEAEs, SAEs, and DLTs
Periodo de tiempo: From time of informed consent until 30 days after the last dose of investigational product.
From time of informed consent until 30 days after the last dose of investigational product.
Occurrence of changes from baseline in patients' clinical safety laboratory values and vital signs to assess the safety and tolerability of STX-003.
Periodo de tiempo: From Day 1 until 30 days after last dose of STX-003
Collection and analysis of changes in data from baseline of patients' safety laboratory values (chemistry, hematology, coagulation, complement (Bb & C3a), urinalysis, and lipids). Vital signs will include Temperature: (degrees Fahrenheit) Pulse: (beats per minute) Respiratory rate: (breaths per minute) Blood pressure: (systolic and diastolic each reported in mmHg) Oxygen saturation by pulse oximetry: (percentage (SpO2, %))
From Day 1 until 30 days after last dose of STX-003

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Assessment of PK and PD in patients dosed with STX-003
Periodo de tiempo: Day 1,2,3,4,8,15,22,23,24,25,29,36, 43,44,51,58
Area under the concentration curve (AUC)
Day 1,2,3,4,8,15,22,23,24,25,29,36, 43,44,51,58
Number and nature of preliminary antitumor activity of STX-003 as monotherapy and in combination with Pembrolizumab.
Periodo de tiempo: From time of informed consent until 30 days after the last dose of investigational product.
From time of informed consent until 30 days after the last dose of investigational product.
Assessment of Tumor infiltrating lymphocytes
Periodo de tiempo: From time if informed consent until 30 days after the last dose of investigational product (STX-003)
Tumor biopsies will be analyzed by immunohistochemistry to assess tumor-infiltrating lymphocytes (TILs) in the tumor microenvironment, including density of CD4 and CD8 positive cells and PD-L1 expression.
From time if informed consent until 30 days after the last dose of investigational product (STX-003)
Objective Response Rate (ORR) in patients with advanced solid tumors.
Periodo de tiempo: From time of informed consent until 30 days after the last dose of investigational product.
From time of informed consent until 30 days after the last dose of investigational product.
Assessment of PK and PD in patients dosed with STX-003
Periodo de tiempo: Day 1,2,3,4,8,15,22,23,24,25,29,36, 43,44,51,58
Maximum observed plasma concentration (Cmax) of STX-003
Day 1,2,3,4,8,15,22,23,24,25,29,36, 43,44,51,58
Changes from baseline in vital signs
Periodo de tiempo: From Day 1 until 30 days after last dose of STX-003.
Vital signs will include Temperature: (degrees Fahrenheit) Pulse: (beats per minute) Respiratory rate: (breaths per minute) Blood pressure: (systolic and diastolic each reported in mmHg) Oxygen saturation by pulse oximetry: (percentage (SpO2, %))
From Day 1 until 30 days after last dose of STX-003.

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)

30 de junio de 2026

Finalización primaria (Estimado)

17 de julio de 2030

Finalización del estudio (Estimado)

15 de noviembre de 2030

Fechas de registro del estudio

Enviado por primera vez

6 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

3 de agosto de 2026

Publicado por primera vez (Actual)

6 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de agosto de 2026

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

3 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

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.

Sí

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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