- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07578077
Golcadomide in Combination With Rituximab for the Treatment of Patients With Relapsed or Refractory Mantle Cell Lymphoma
A Phase 1/2 Study of the CELMoD Agent Golcadomide in Combination With Rituximab in Patients With Relapsed or Refractory Mantle Cell Lymphoma
Descripción general del estudio
Estado
Descripción detallada
PRIMARY OBJECTIVES:
I. To evaluate the safety and tolerance of golcadomide in mantle cell lymphoma (MCL) patients who were resistant or intolerant to covalent bruton's tyrosine kinase inhibitors (cBTKi).
II. To evaluate the safety and tolerance of golcadomide in combination with rituximab in MCL patients who were resistant or intolerant to cBTKi.
III. To estimate the efficacy of golcadomide and rituximab in MCL patients who were resistant or intolerant to cBTKi.
SECONDARY OBJECTIVES:
I. To evaluate the complete response rate (CR) of the combination of golcadomide and rituximab.
II. To evaluate the durability of response by the duration of response (DOR) and duration of complete response (DOCR).
EXPLORATORY OBJECTIVES:
I. Correlate clinical response with changes in baseline T cell characteristics and cytokine profiles.
II. To measure the rate of minimal residual disease undetectability in responding patients.
OUTLINE: This is a phase I, dose-escalation study of golcadomide followed by a phase II study. Patients are assigned to 1 of 2 phases.
PHASE I: Patients receive golcadomide orally (PO) once daily (QD) on days 1-14 of each cycle. Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and positron emission tomography (PET)/computed tomography (CT) throughout the trial. Patients undergo bone marrow biopsy and may undergo tissue biopsy on study.
PHASE II: Patients receive golcadomide PO QD on days 1-14 of each cycle. Patients also receive rituximab intravenously (IV) on days 1, 8, 15 and 22 of cycle 1 and then day 1 of even cycles. Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and PET/CT throughout the trial. Patients undergo bone marrow biopsy and may undergo tissue biopsy on study.
After completion of study treatment, patients are followed up at 30 days, and then up to 3 years.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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California
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Duarte, California, Estados Unidos, 91010
- City of Hope Medical Center
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Investigador principal:
- Tycel J. Phillips
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Contacto:
- Tycel J. Phillips
- Número de teléfono: 82405 626-256-4673
- Correo electrónico: tphillips@coh.org
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Documented informed consent of the participant and/or legally authorized representative
Agreement to allow the use of archival tissue from diagnostic tumor biopsies
- If unavailable, exceptions may be granted with study principal investigator (PI) approval
- Ability to adhere to the study protocol
- Age: ≥ 18 years
- Eastern Clinical Oncology Group (ECOG) ≤ 2
Histologically confirmed diagnosis of MCL
- Immunohistochemistry of the biopsy
- Flow cytometry of the biopsy
- Relapsed/ refractory disease
- Relapsed/refractory (R/R) MCL after at least one line of therapy including resistant or intolerant to a cBTKi
- Fully recovered from the acute toxic effects (except alopecia) to ≤ grade 1 to prior anti-cancer therapy
- Ability to swallow pills
Without bone marrow involvement: Absolute neutrophil count (ANC) > 1.5 × 10^9/L (ANC > 1,500/mm^3)
- With bone marrow involvement: ANC > 1.0 × 10^9/L (ANC > 1000/mm^3)
- NOTE: Growth factor is not permitted within 14 days of ANC assessment unless cytopenia is secondary to disease involvement. For patients with significant marrow involvement, eligibility may be confirmed at the discretion of the treating investigator
Without bone marrow involvement: Platelets ≥ 75,000/mm^3
- With bone marrow involvement: Platelets ≥ 50,000/mm^3
- NOTE: Platelet transfusions are not permitted within 14 days of platelet assessment unless cytopenia is secondary to disease involvement
- Total bilirubin ≤ 1.5 × upper limit of normal (ULN) (≤ 1.5 × ULN if Gilbert's disease)
- Aspartate aminotransferase (AST) =< 2.5 × ULN
- Alanine aminotransferase (ALT) ≤ 2.5 × ULN unless elevation is attributable to underlying disease, in which case ALT ≤ 3.0 × ULN
- Creatinine clearance of ≥ 30 mL/min per 24 hour urine test or the Cockcroft-Gault formula
- If not receiving anticoagulants: International normalized ratio (INR) OR prothrombin (PT) ≤ 1.5 × ULN. If on anticoagulant therapy: PT must be within therapeutic range of intended use of anticoagulants
- If not receiving anticoagulants: Activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN. If on anticoagulant therapy: aPTT must be within therapeutic range of intended use of anticoagulants
- Seronegative for HIV
- Seronegative for hepatitis C virus (HCV), hepatitis B virus (HBV) (surface antigen negative)
Meets other institutional and federal requirements for infectious disease titer requirements
- Note Infectious disease testing to be performed within 28 days prior to day 1 of protocol therapy
- Woman of childbearing potential must have a negative pregnancy test using a highly sensitive assay (minimum sensitivity 25 IU/L) performed within 10 to 14 days and again within 24 hours prior to receiving the first dose of golcadomide/BMS-986369
Agreement by females of childbearing potential to use two effective methods of contraception simultaneously without interruption, for at least 28 days before starting study treatment, throughout the entire duration of study treatment, during dose interruptions, and for at least 28 days after the last dose of golcadomide/BMS-986369. The two methods of contraception must include one highly effective method and one additional effective method. Compliance will be documented using the Clinical Trial Pregnancy Risk Awareness Checklist, which must be completed and provided to participants at screening and prior to dispensing of study drug. An individual of childbearing potential (IOCBP) is defined as:
- A person who has achieved menarche, has not undergone a documented hysterectomy or bilateral oophorectomy, and has not been naturally postmenopausal for at least 12 consecutive months. Amenorrhea resulting from medical interventions (such as cancer therapy), rather than natural menopause, does not exclude childbearing potential.
Criteria:
- Achievement of menarche (onset of menstruation).
No history of surgical sterilization:
- No documented hysterectomy
- No documented bilateral oophorectomy
Not naturally postmenopausal:
- Defined as absence of menses for ≥ 12 consecutive months due to natural causes (not due to medical interventions such as chemotherapy, hormonal therapy, or radiotherapy)
- Amenorrhea due to medical causes (e.g., cancer therapy, hormonal treatment) does not qualify as natural menopause and does not exclude childbearing potential
Exclusion Criteria:
- Chemotherapy, radiation therapy (except for palliative radiation therapy [XRT]), biological therapy, immunotherapy within 21 days or five half-lives (whichever is shorter for non-radiation therapy) prior to day 1 of protocol therapy
- Strong CYP3A4 inducers/ inhibitors within 14 days prior to day 1 of protocol therapy
- Herbal medications
- History of metastatic cancer
Unstable cardiac disease as defined by one of the following:
- Cardiac events such as myocardial infarction (MI) within the past 6 months
- New York Heart Association (NYHA) heart failure class III-IV
- Uncontrolled atrial fibrillation or hypertension
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to study agents
- Clinically significant uncontrolled illness
- Known seropositive or active infection with HIV, HBV, or HCV
- Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) at study enrollment or any major episode of infection (as evaluated by the investigator) within 4 weeks prior to the first study treatment
- Females only: Pregnant or breastfeeding
- Any other condition that would, in the investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures
- Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Phase I (Golcadomide)
Patients receive golcadomide PO QD on days 1-14 of each cycle.
Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity.
Patients also undergo blood sample collection and PET/CT throughout the trial.
Patients undergo bone marrow biopsy and may undergo tissue biopsy on study.
|
Someterse a la recolección de muestras de sangre
Otros nombres:
Someterse a PET/CT
Otros nombres:
Someterse a PET/CT
Otros nombres:
Someterse a una biopsia de médula ósea
Otros nombres:
Orden de compra dada
Otros nombres:
Sufrir biopsia de tejido
Otros nombres:
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Experimental: Phase II (Golcadomide, rituximab)
Patients receive golcadomide PO QD on days 1-14 of each cycle.
Patients also receive rituximab IV on days 1, 8, 15 and 22 of cycle 1 and then day 1 of even cycles.
Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity.
Patients also undergo blood sample collection and PET/CT throughout the trial.
Patients undergo bone marrow biopsy and may undergo tissue biopsy on study.
|
Someterse a la recolección de muestras de sangre
Otros nombres:
Dado IV
Otros nombres:
Someterse a PET/CT
Otros nombres:
Someterse a PET/CT
Otros nombres:
Someterse a una biopsia de médula ósea
Otros nombres:
Orden de compra dada
Otros nombres:
Sufrir biopsia de tejido
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Incidence of dose limiting toxicities (DLT)
Periodo de tiempo: During cycle 1 (Cycle length = 28 days)
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The adverse events will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0 (NCI CTCAE v 5.0).
Toxicity will be summarized by type, severity, and attribution.
DLT will be individually described.
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During cycle 1 (Cycle length = 28 days)
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Maximum tolerated dose (MTD) of golcadomide
Periodo de tiempo: Up to 3 years
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If single agent is tolerable, we will subsequently explore golcadomide in combination with rituximab.
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Up to 3 years
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MTD of golcadomide in combination with rituximab
Periodo de tiempo: Up to 3 years
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Patients would remain on therapy until unacceptable toxicity, treating physician discretion or PD.
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Up to 3 years
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Overall response rate (ORR)
Periodo de tiempo: Up to 3 years
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Defined as achieving a best response of either complete metabolic response (CMR) or partial metabolic response (PMR) in a response-evaluable participant after the start of protocol therapy and prior to disease progression and/or start of other anti-lymphoma therapy.
ORR will be estimated by binary proportions, along with the 95% exact binomial confidence intervals.
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Up to 3 years
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Progression free survival (PFS)
Periodo de tiempo: From start of protocol treatment to time of disease relapse/progression or death due to any cause, whichever occurs earlier, assessed up to 3 years
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PFS will be estimated using the product-limit method of Kaplan and Meier along with the Greenwood estimator of standard error; 95% confidence interval will be constructed based on log-log transformation.
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From start of protocol treatment to time of disease relapse/progression or death due to any cause, whichever occurs earlier, assessed up to 3 years
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Incidence of adverse events
Periodo de tiempo: Up to 3 years
|
Will be graded by NCI CTCAE v 5.0.
Toxicity will be summarized by type, severity, and attribution.
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Up to 3 years
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Duration of response (DOR) of the combination of golcadomide and rituximab
Periodo de tiempo: From the first achievement of PMR or CMR to time of progressive disease (PD) or death, whichever earlier, assessed up to 3 years
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DOR will be estimated using the product-limit method of Kaplan and Meier.
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From the first achievement of PMR or CMR to time of progressive disease (PD) or death, whichever earlier, assessed up to 3 years
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Duration of complete response (DOCR) of the combination of golcadomide and rituximab
Periodo de tiempo: Time from the first achievement of CMR to time of PD or death, whichever earlier, assessed up to 3 years
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DOCR will be estimated using the product-limit method of Kaplan and Meier.
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Time from the first achievement of CMR to time of PD or death, whichever earlier, assessed up to 3 years
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Complete response (CR) of the combination of golcadomide and rituximab
Periodo de tiempo: Up to 3 years
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CR rate will be estimated by binary proportions, along with the 95% exact binomial confidence intervals.
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Up to 3 years
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Tycel J Phillips, City of Hope Medical Center
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Neoplasias
- Enfermedades del sistema inmunológico
- Neoplasias por tipo histológico
- Enfermedades linfáticas
- Trastornos linfoproliferativos
- Trastornos inmunoproliferativos
- Linfoma No Hodgkin
- Linfoma
- Enfermedades hemic y linfáticas
- Linfoma De Células Del Manto
- Aminoácidos, péptidos y proteínas
- Proteínas
- Técnicas de investigación
- Técnicas de laboratorio clínico
- Técnicas y procedimientos de diagnóstico
- Diagnóstico
- Procedimientos quirúrgicos, operativo
- Técnicas citológicas
- Citodiagnóstico
- Anticuerpos, monoclonal
- Anticuerpos
- Inmunoglobulinas
- Inmunoproteínas
- Proteínas de la sangre
- Globulinas séricas
- Globulinas
- Técnicas de diagnóstico, quirúrgico
- Técnicas de química, analítica
- Análisis de espectro
- Anticuerpos, monoclonales, derivados de murino
- Rituximab
- Biopsia
- Manejo de muestras
- Espectroscopía de resonancia magnética
- CT-P10
Otros números de identificación del estudio
- 25448 (Otro identificador: City of Hope Medical Center)
- P30CA033572 (Subvención/contrato del NIH de EE. UU.)
- NCI-2026-02921 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
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.
producto fabricado y exportado desde los EE. UU.
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