A Study in Participants With Relapsed or Refractory Multiple Myeloma for QLS4131
A Phase 3 Randomized Study Comparing QLS4131 Injection Versus Treatment Per Investigator's Choice in Participants With Relapsed or Refractory Multiple Myeloma
The purpose of this clinical trial is to evaluate the efficacy and safety of QLS4131 compared with the investigator's choice regimen (DPd or PVd) in participants with relapsed or refractory multiple myeloma (RRMM).
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
This study is an open, multicenter, randomized controlled phase III clinical trial aimed at evaluating the efficacy and safety of QLS4131 compared to the investigator's choice regimen (DPd or PVd) in participants with relapsed or refractory multiple myeloma who have previously received 1-4 lines of therapy and have been exposed to three classes of drugs (proteasome inhibitors, immunomodulators, and anti-CD38 monoclonal antibodies). The plan is to enroll approximately 300 participants, who will be randomly assigned to the experimental group and the control group in a 1:1 ratio. Approximately 150 participants in the experimental group will receive QLS4131 treatment, while about 150 participants in the control group will receive the investigator's choice of treatment (DPd or PVd).
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- Fase 3
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: LUGUI QIU, Doctor of Medicine (MD)
- Número de teléfono: 022-23608124
- Correo electrónico: qiulg@ihcams.ac.cn
Copia de seguridad de contactos de estudio
- Nombre: GANG AN, Doctor of Medicine (MD)
- Número de teléfono: 13502181109
- Correo electrónico: angang@ihcams.ac.cn
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Age ≥18 years.
- Documented initial diagnosis of multiple myeloma according to IMWG diagnostic criteria.
- At least one of the following measurable disease indicators:
- Serum M-protein ≥ 5 g/L
- Urine M-protein ≥200 mg/24h
- Serum free light chain (FLC) test: affected FLC level ≥100 mg/L and abnormal serum FLC ratio.
- Received 1-4 prior lines of therapy, including a proteasome inhibitor (PI), an immunomodulatory drug, and an anti-CD38 monoclonal antibody (mAb).
- Willing and able to comply with the prohibitions and restrictions specified in this protocol.
Exclusion Criteria:
- Prior treatment with both the BCMA-targeted therapy and the GPRC5D-targeted therapy. Patients who have received either BCMA-targeted or GPRC5D-targeted therapy alone are eligible.
- Known hypersensitivity to any of the ingredients of investigational drug.
- Diagnosis of plasma cell leukemia(peripheral blood plasma cells ≥5%),or primary light chain amyloidosis.
- Known active central nervous system (CNS) involvement, or clinical signs and symptoms suggestive of meningeal involvement by multiple myeloma.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- 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: QLS4131
Participants will receive QLS4131 injection until death, disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent to participate in the study, or other reasons for discontinuation of study treatment, whichever occurs first. |
QLS4131 will be administered subcutaneously. |
|
Comparador activo: The investigator's choice regimen (DPd or PVd )
Participants will receive DPd or PVd until death, disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent to participate in the study, or other reasons for discontinuation of study treatment, whichever occurs first. |
The DPd treatment regimen, one cycle every 28 days: Pomalidomide 4mg/d orally, on days 1-21;The PVd treatment regimen, one cycle every 21 days: Pomalidomide 4 mg/d orally, on days 1-14 of each treatment cycle. The PVd treatment regimen, with one cycle every 21 days: Bortezomib on days 1, 4, 8, and 11 of cycles 1-8, and on days 1 and 8 from cycle 9 onwards. The DPd treatment regimen, one cycle every 28 days: on days 1, 8, 15, and 22 of cycles 1 and 2; on days 1 and 15 from cycles 3-6; and on day 1 from cycle 7 onwards. The DPd treatment regimen, one cycle every 28 days: Dexamethasone 20 mg orally, on days 1, 2, 8, 9, 15, 16, 22, and 23 (total 40 mg per week). The PVd treatment regimen, one cycle every 21 days: Dexamethasone 20 mg orally, on days 1, 2, 4, 5, 8, 9, 11, and 12 of cycles 1-8, and on days 1, 2, 8, and 9 from cycle 9 onwards. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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PFS assessed by independent review committee
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
PFS is defined as the duration from the date of randomization to either PD or death, whichever comes first. Disease progression will be determined according to the IMWG 2016 response criteria. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
PFS assessed by investigator
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
PFS is defined as the duration from the date of randomization to either PD or death, whichever comes first. Disease progression will be determined according to the IMWG 2016 response criteria. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
Very good partial response or better rate
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
Very good partial response or better rate is defined as the percentage of participants who achieve very good partial response or better prior to subsequent antimyeloma therapy in accordance with the IMWG 2016 response criteria. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
Negativity rate of minimal residual disease (MRD)
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
Defined as the proportion of participants achieving MRD-negative status. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
Sustained MRD negativity rate
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
Defined as the proportion of participants achieving MRD-negative status and maintaining it for at least 1 year. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
6-month MRD negativity rate
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
The proportion of participants achieving a response of CR or better and MRD-negative status at 6 months post-randomization. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
12-month MRD negativity rate
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
The proportion of participants achieving a response of CR or better and MRD-negative status at 12 months post-randomization. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
Objective response rate
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
Objective response rate is defined as the percentage of participants who achieve PR or better prior to subsequent antimyeloma therapy in accordance with the IMWG 2016 response criteria. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
Complete response or better rate
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
Complete response or better rate is defined as the percentage of participants who achieve CR or better prior to subsequent antimyeloma therapy in accordance with the IMWG 2016 response criteria. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
Duration of response
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
DoR is defined as the time interval between the date of initial documentation of a response (PR or better) to the date of first documented evidence of progressive disease according to the IMWG 2016 response criteria or death from any cause. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
PFS Rate at 6, 12, and 18 Months
Periodo de tiempo: 6, 12, and 18 months after randomization
|
Percentage of participants who remain alive and progression-free at 6, 12, and 18 months after randomization, as assessed by both the independent review committee (IRC) and the investigator according to IMWG 2016 response criteria. |
6, 12, and 18 months after randomization
|
|
Overall survival
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
OS is defined as the time from the date of randomization to the date of the participant's death due to any cause. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
OS Rate at 12 and 24 Months
Periodo de tiempo: 12 and 24 months after randomization
|
Percentage of participants who remain alive at 12 and 24 months after randomization. |
12 and 24 months after randomization
|
|
Number of Participants with Treatment-Emergent Adverse events (TEAE) by Severity
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
Number of participants with AEs by Severity will be reported. |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
|
Change from Baseline in Symptoms, Functioning, and Overall Health-related Quality of Life (HRQoL) as Assessed by European Organization for Research and Treatment of Cancer Quality-of-life Questionnaire Core 30 (EORTC-QLQ-C30)
Periodo de tiempo: up to 2 years after the last enrolled participant receives the first dose of study drug
|
Change from baseline scores |
up to 2 years after the last enrolled participant receives the first dose of study drug
|
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
- Enfermedades Vasculares
- Enfermedades cardiovasculares
- Procesos Patológicos
- Neoplasias
- Atributos de la enfermedad
- Enfermedades del sistema inmunológico
- Neoplasias por tipo histológico
- Enfermedades hematológicas
- Trastornos linfoproliferativos
- Trastornos inmunoproliferativos
- Neoplasias De Células Plasmáticas
- Trastornos hemostáticos
- Paraproteinemias
- Trastornos de proteínas en sangre
- Trastornos hemorrágicos
- Condiciones Patológicas, Signos y Síntomas
- Enfermedades hemic y linfáticas
- Reaparición
- Mieloma múltiple
- Químicos orgánicos
- Compuestos heterocíclicos, 1 anillo
- Compuestos heterocíclicos
- Terapéutica
- Rutas de administración de drogas
- Terapia con drogas
- Compuestos policíclicos
- Químicos inorgánicos
- Espierra
- Embarazos
- Esteroides
- Compuestos de anillo fusionado
- Esteroides, fluorado
- Esparrazadienetrioles
- Ácidos borónicos
- Ácidos, no carboxílicos
- Ácidos
- Compuestos de boro
- Pirazinas
- Bortezomib
- Dexametasona
- Inyecciones
- pomalidomida
- daratumumab
- Inyecciones, subcutáneas
Otros números de identificación del estudio
Otros números de identificación del estudio
- QLS4131-301
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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