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A Clinical Study of MHB034C for Injection in Participants With Advanced Solid Tumors

4 de noviembre de 2026 actualizado por: Minghui Pharmaceutical (Shanghai) LTD

A Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of MHB034C for Injection in Participants With Advanced Solid Tumors

This study is an open-label, multicenter, first-in-human (FIH) Phase I/II clinical study to evaluate the safety, tolerability, pharmacokinetic (PK) profile, and preliminary efficacy of MHB034C in participants with advanced solid tumors.

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Descripción detallada

The phaseI/II study consists of two stages: a dose escalation stage and a dose expansion stage. The primary objective of the Phase I dose escalation stage is to evaluate the safety and tolerability of MHB034C in participants with advanced solid tumors; the primary objective of the Phase II dose expansion stage is to evaluate the antitumor efficacy of MHB034C in selected participants with advanced solid tumors.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

400

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

Ubicaciones de estudio

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Porcelana, 201419
        • Fudan University Shanghai Cancer Center
        • Contacto:
          • Ethics Committee
          • Número de teléfono: 85033 +86 021-64175590
          • Correo electrónico: JJYIN555@163.com

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

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  1. Participants voluntarily agree to participate in this study and sign the informed consent form.
  2. Aged ≥ 18 years, regardless of sex.
  3. ECOG Performance Status (PS) score of 0-1.
  4. Life expectancy of more than 3 months.
  5. Female participants of childbearing potential, and male participants whose partners are women of childbearing potential, must agree to use highly effective contraception with their partners; must refrain from donating gametes, from initiating gamete cryopreservation, and from retrieving or using their own previously cryopreserved gametes for conception. Female participants of childbearing potential must have a negative serum β-HCG pregnancy test within 7 days prior to the first use of the investigational medicinal product (IMP), and must not be lactating.
  6. Ability to understand the study requirements and willingness and ability to comply with the study and follow-up procedures.
  7. Participants enrolled in the Phase I dose escalation stage must have advanced solid tumors confirmed by histopathological or cytological examination, and must have progressed on or been intolerant to standard therapy, or have no standard treatment available.
  8. Participants enrolled in the Phase II dose expansion stage must have advanced solid tumors confirmed by histopathological or cytological examination, and must have progressed on or been intolerant to standard therapy, or have no standard treatment available.
  9. During the dose escalation stage, the investigator should make best efforts to obtain consent from participants to provide pre-treatment tumor tissue samples; during the dose expansion stage, participants must agree to provide pre-treatment tumor tissue samples, and if such samples cannot be provided, enrolment is permitted only with the sponsor's approval.
  10. At least one measurable tumor lesion according to the RECIST v1.1 criteria.
  11. Adequate bone marrow function.
  12. Adequate hepatic function.
  13. Adequate renal function.
  14. Adequate coagulation function.
  15. Adequate cardiac function.

Exclusion Criteria:

  1. Has had another primary malignancy within 3 years prior to signing the informed consent form, excluding early-stage malignancies that have been curatively treated.
  2. Has previously used or is currently using an antibody-drug conjugate (ADC) with a topoisomerase I inhibitor as the payload, with certain exceptions.
  3. Has previously received doxorubicin at a cumulative dose of > 360 mg/m² or an equivalent dose of a similar agent.
  4. Has received chemotherapy or endocrine therapy within 3 weeks, or radiotherapy, biological therapy, immunotherapy, or other anti-tumor therapy within 4 weeks, prior to the first dose of the investigational medicinal product .
  5. Has spinal cord compression, leptomeningeal metastasis, brainstem metastasis, or unstable brain metastasis.
  6. Adverse events from prior anti-tumor therapy have not resolved to ≤ Grade 1 as assessed by NCI-CTCAE v6.0.
  7. Has undergone major surgery on a major organ (excluding biopsy) or experienced significant trauma within 4 weeks prior to the first use of the IMP, or requires elective surgery during the study period, or currently has severe unhealed or dehiscent wounds, active and clinically significant ulcers, untreated fractures, or active unhealed stomatitis.
  8. Has received a live vaccine or live attenuated vaccine within 4 weeks prior to the first use of the IMP.
  9. Has received or requires systemic corticosteroids or other immunosuppressive therapy within 14 days prior to the first use of the IMP, excluding topical, ophthalmic, intra-articular, intranasal, and inhaled corticosteroid therapy, and short-term corticosteroid use for prophylaxis.
  10. Has moderate or severe pulmonary disease that significantly impairs pulmonary function.
  11. Has a history of interstitial lung disease/pneumonitis (ILD), currently has ILD, or suspected ILD that cannot be ruled out by imaging during screening.
  12. Has severe cardiovascular disease or high-risk factors.
  13. Has experienced an arterial/venous thrombotic event within 6 months prior to the first dose.
  14. Has a clinically evident or uncontrolled third-space fluid collection requiring repeated drainage.
  15. Currently has an active autoimmune disease, or has a history of active autoimmune disease requiring systemic immunosuppressive therapy within 2 years prior to the first use of the IMP.
  16. Has clinically significant corneal disease, or is currently using other medications that may cause corneal damage.
  17. Has an active infection requiring systemic therapy within 7 days prior to the first dose.
  18. Has clinically uncontrolled diabetes mellitus.
  19. Has active tuberculosis, or a history of tuberculosis infection that was not controlled after treatment, or is still receiving anti-tuberculosis therapy; or has active syphilis.
  20. Positive serological virology results: positive for HIV antibody; or positive for HBsAg or HBcAb with HBV-DNA ≥ 500 IU/mL; or positive for HCV antibody with positive HCV-RNA.
  21. Has experienced clinically significant bleeding symptoms or an obvious bleeding tendency within 1 month prior to the first dose.
  22. Has known hypersensitivity or delayed hypersensitivity to certain components or analogues of the IMP in this study.
  23. Has a history of severe neurological or psychiatric disorders, or a history of psychotropic substance abuse or drug abuse, or any other medical condition.
  24. Has known alcohol or drug dependence.
  25. Has insufficient compliance to participate in this clinical study in the investigator's judgment, or the investigator considers that the participant has a history of other serious systemic diseases or other conditions unsuitable for participation in this study.

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: MHB034C for Injection

MHB034C for Injection

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Phase I Dose Escalation Stage: Incidence of DLT
Periodo de tiempo: At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
Phase I Dose Escalation Stage: Incidence of Adverse events (AEs)
Periodo de tiempo: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase I Dose Escalation Stage: Incidence of Serious adverse events (SAEs)
Periodo de tiempo: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase I Dose Escalation Stage: MTD
Periodo de tiempo: At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
Phase I Dose Escalation Stage: RP2D
Periodo de tiempo: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: ORR as assessed by the investigator per RECIST v1.1.
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: DCR as assessed by the investigator per RECIST v1.1.
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: DoR as assessed by the investigator per RECIST v1.1.
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: PFS as assessed by the investigator per RECIST v1.1.
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: OS as assessed by the investigator per RECIST v1.1.
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: PFS rates at 6 and 12 months.
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: OS rates at 6 and 12 months.
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Phase I Dose Escalation Stage: AUC0-t、AUC0-∞ of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Cmax of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Tmax of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: CL of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: t1/2 of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Vss of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Ctrough of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage and Phase II Dose Expansion Stage: Positivity rate of anti-MHB034C antibodies (ADA) and their possible neutralizing antibodies (NAb)
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: ORR as assessed by the investigator per RECIST v1.1
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: DCR as assessed by the investigator per RECIST v1.1
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: DoR as assessed by the investigator per RECIST v1.1
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: PFS as assessed by the investigator per RECIST v1.1
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: OS as assessed by the investigator per RECIST v1.1
Periodo de tiempo: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: Incidence of AEs
Periodo de tiempo: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: Incidence of SAEs
Periodo de tiempo: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: Concentrations of total antibody, ADC, and free payload in participants after dosing
Periodo de tiempo: through study completion, an average of 2 years
through study completion, an average of 2 years

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 (Estimado)

20 de diciembre de 2026

Finalización primaria (Estimado)

15 de junio de 2028

Finalización del estudio (Estimado)

19 de mayo de 2029

Fechas de registro del estudio

Enviado por primera vez

29 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

4 de noviembre de 2026

Publicado por primera vez (Actual)

10 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

10 de noviembre de 2026

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

4 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • MHB034C-A-101

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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