A Clinical Study of MHB034C for Injection in Participants With Advanced Solid Tumors
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
Estado
Condiciones
Condiciones
Intervención / Tratamiento
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
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: VP of R&D
- Número de teléfono: +86 021-60898367
- Correo electrónico: jwshi@minghuipharma.com
Ubicaciones de estudio
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Porcelana, 201419
- Fudan University Shanghai Cancer Center
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Contacto:
- Ethics Committee
- Número de teléfono: 85033 +86 021-64175590
- Correo electrónico: JJYIN555@163.com
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Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Participants voluntarily agree to participate in this study and sign the informed consent form.
- Aged ≥ 18 years, regardless of sex.
- ECOG Performance Status (PS) score of 0-1.
- Life expectancy of more than 3 months.
- 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.
- Ability to understand the study requirements and willingness and ability to comply with the study and follow-up procedures.
- 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.
- 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.
- 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.
- At least one measurable tumor lesion according to the RECIST v1.1 criteria.
- Adequate bone marrow function.
- Adequate hepatic function.
- Adequate renal function.
- Adequate coagulation function.
- Adequate cardiac function.
Exclusion Criteria:
- Has had another primary malignancy within 3 years prior to signing the informed consent form, excluding early-stage malignancies that have been curatively treated.
- Has previously used or is currently using an antibody-drug conjugate (ADC) with a topoisomerase I inhibitor as the payload, with certain exceptions.
- Has previously received doxorubicin at a cumulative dose of > 360 mg/m² or an equivalent dose of a similar agent.
- 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 .
- Has spinal cord compression, leptomeningeal metastasis, brainstem metastasis, or unstable brain metastasis.
- Adverse events from prior anti-tumor therapy have not resolved to ≤ Grade 1 as assessed by NCI-CTCAE v6.0.
- 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.
- Has received a live vaccine or live attenuated vaccine within 4 weeks prior to the first use of the IMP.
- 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.
- Has moderate or severe pulmonary disease that significantly impairs pulmonary function.
- Has a history of interstitial lung disease/pneumonitis (ILD), currently has ILD, or suspected ILD that cannot be ruled out by imaging during screening.
- Has severe cardiovascular disease or high-risk factors.
- Has experienced an arterial/venous thrombotic event within 6 months prior to the first dose.
- Has a clinically evident or uncontrolled third-space fluid collection requiring repeated drainage.
- 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.
- Has clinically significant corneal disease, or is currently using other medications that may cause corneal damage.
- Has an active infection requiring systemic therapy within 7 days prior to the first dose.
- Has clinically uncontrolled diabetes mellitus.
- 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.
- 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.
- Has experienced clinically significant bleeding symptoms or an obvious bleeding tendency within 1 month prior to the first dose.
- Has known hypersensitivity or delayed hypersensitivity to certain components or analogues of the IMP in this study.
- Has a history of severe neurological or psychiatric disorders, or a history of psychotropic substance abuse or drug abuse, or any other medical condition.
- Has known alcohol or drug dependence.
- 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
¿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)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
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Experimental: MHB034C for Injection
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MHB034C for Injection |
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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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)
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At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
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Phase I Dose Escalation Stage: Incidence of Adverse events (AEs)
Periodo de tiempo: from Day1 to 30 days after last dose
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from Day1 to 30 days after last dose
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Phase I Dose Escalation Stage: Incidence of Serious adverse events (SAEs)
Periodo de tiempo: from Day1 to 30 days after last dose
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from Day1 to 30 days after last dose
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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)
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At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
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Phase I Dose Escalation Stage: RP2D
Periodo de tiempo: from Day1 to 30 days after last dose
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from Day1 to 30 days after last dose
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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
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One year after the last subject was enrolled in the group
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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
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One year after the last subject was enrolled in the group
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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
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One year after the last subject was enrolled in the group
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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
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One year after the last subject was enrolled in the group
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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
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One year after the last subject was enrolled in the group
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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
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One year after the last subject was enrolled in the group
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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
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One year after the last subject was enrolled in the group
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Phase I Dose Escalation Stage: AUC0-t、AUC0-∞ of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
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through study completion, an average of 2 years
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Phase I Dose Escalation Stage: Cmax of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
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through study completion, an average of 2 years
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Phase I Dose Escalation Stage: Tmax of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
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through study completion, an average of 2 years
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Phase I Dose Escalation Stage: CL of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
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through study completion, an average of 2 years
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Phase I Dose Escalation Stage: t1/2 of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
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through study completion, an average of 2 years
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Phase I Dose Escalation Stage: Vss of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
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through study completion, an average of 2 years
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Phase I Dose Escalation Stage: Ctrough of MHB034C
Periodo de tiempo: through study completion, an average of 2 years
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through study completion, an average of 2 years
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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
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through study completion, an average of 2 years
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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
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One year after the last subject was enrolled in the group
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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
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One year after the last subject was enrolled in the group
|
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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
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One year after the last subject was enrolled in the group
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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
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One year after the last subject was enrolled in the group
|
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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
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One year after the last subject was enrolled in the group
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Phase II Dose Expansion Stage: Incidence of AEs
Periodo de tiempo: from Day1 to 30 days after last dose
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from Day1 to 30 days after last dose
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Phase II Dose Expansion Stage: Incidence of SAEs
Periodo de tiempo: from Day1 to 30 days after last dose
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from Day1 to 30 days after last dose
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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
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through study completion, an average of 2 years
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- MHB034C-A-101
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.
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