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Golcadomide With Pemetrexed, Rituximab, and Dexamethasone for Relapsed and Refractory CNS Lymphomas

19 de agosto de 2026 actualizado por: Allison Winter

Phase I Pilot Trial of Golcadomide With Pemetrexed, Rituximab, and Dexamethasone for Relapsed and Refractory CNS Lymphomas

This research study is for people who have been diagnosed with large B-cell lymphoma of the central nervous system (CNS), which has either returned or is not responding to current treatment. Goldcadomide is a new experimental drug that works by binding to a specific protein inside cancer cells and helps stimulate immune cells that help fight cancer cells. It also has the ability to enter the central nervous system. It has shown promising safety and effectiveness when combined with standard of care chemotherapy. Participants will be treated with this study drug combined with standard of care chemotherapy. Participation in the research will last about 2.5 years. The purpose of this study is to help researchers learn if the study drug, Golcadomide, in combination with the standard of care regimen is a safe and effective way to treat large B-cell lymphoma with CNS involvement.

Descripción general del estudio

Descripción detallada

People with systemic diffuse large B-cell lymphoma (DLCBL) can either have a a disease that involves the central nervous system or does not involve the central nervous system. The disease could also be only located in the central nervous system. The central nervous system lymphoma includes disease within the brain, meninges, cranial nerves, cerebrospinal fluid, spinal cord, and/or intraocular. For people with disease that involves the CNS it can be difficult to treat. This is because many effective lymphoma treatments do not cross the blood-brain barrier (BBB).

In general there is a large unmet need for effective and feasible therapies for CNS lymphomas. This study addresses these gaps by combining standard of care chemotherapy with Golcadomide.This approach aims to provide a feasible and potentially effective treatment option for a population with historically poor outcomes.

The purpose of this study is to find out the safety and efficacy of Golcadomide in combination with drugs in the standard care chemotherapy. Another goal is to find the recommended phase 2 dose of Golcadomide in combination with standard of care chemotherapy.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

18

Fase

  • 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: Allison M Winter, MD
  • Número de teléfono: (216) 445-4635
  • Correo electrónico: wintera2@ccf.org

Ubicaciones de estudio

    • Ohio
      • Cleveland, Ohio, Estados Unidos, 44122
        • Cleveland Clinic, Case Comprehensive Cancer Center
        • Investigador principal:
          • Allison Winter, MD
        • Contacto:
          • Allison M Winter, MD
          • Número de teléfono: (216) 445-4635
          • Correo electrónico: wintera2@ccf.org

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:

  • Participants or their legally acceptable representative must have signed and dated an IRB approved written ICF in accordance with regulatory, local, and institutional guidelines.
  • Participants ≥ 18 years of age.
  • Confirmed histopathological diagnosis of aggressive malignant B-cell lymphoma based upon a representative histology specimen according to the WHO classification. For participants with secondary CNS lymphoma, this can be confirmed by prior systemic biopsy. If a CNS lesion was not amenable for biopsy, imaging (e.g. MRI Brain ± MRI Full Spine) with CSF analysis for cytology may be used to confirm diagnosis, in lieu of a biopsy. Required. Acceptable histologies include:

    • Large B-cell lymphoma NOS
    • Diffuse large B-cell lymphoma (including GCB and ABC types)
    • High-grade B-cell lymphoma with MYC and BCL2 rearrangements (double hit lymphomas)
    • High-grade B-cell lymphoma NOS
    • T-cell/histiocyte/rich large B-cell lymphoma (THRLBCL)
    • EBV + DLBCL
    • PMBCL
    • Follicular Large B-Cell (previously referred to as Follicular Lymphoma, Grade 3B)
  • Participants must have active CNS lymphoma for which this trial is planned. Confirmation of the histology in relapsed setting is not required but participants must have measurable disease per the International PCSNL Collaboration Group Criteria (Section 11.1), as evidenced by at least one of the following:

    • CNS disease on MRI (brain or spine including parenchymal and leptomeningeal)
    • Detectable in the CSF
    • Detectable on ophthalmologic exam
  • Participants must have received ≥ 1 prior systemic therapy for treatment of their CNS lymphoma. Participants who had systemic lymphoma and then relapsed with secondary CNS lymphoma must have received at least one prior line of therapy to specifically treat the CNS lymphoma.
  • Participants must have received prior high dose methotrexate as a line of therapy OR have been ineligible for methotrexate therapy based on the investigator's discretion.

    • Participants who have received methotrexate as their first line of therapy but are no longer eligible for ongoing methotrexate and have persistent disease are eligible
  • ECOG performance status ≤ 0-3. PS 3 is allowed if it is disease related and not due to comorbidities or frailty and PS 4 is allowed if it is from CNS causing motor weakness and not due to comorbidities or frailty. (see Appendix I)
  • Adequate bone marrow function, defined by the following laboratory parameters:

    • Absolute neutrophil ≥ 1.5 x 109/L
  • Platelet count ≥ 100 x 109/L

    • Hemoglobin ≥ 8 g/dL
  • Adequate organ function, defined by the following laboratory parameters:

    • Adequate hepatic function, with transaminases (alanine aminotransferase [ALT], aspartate aminotransferase [AST], and gamma glutamyl transferase [GGT]) ≤ 2.5 times the upper limit of normal
  • Bilirubin ≤1.5 x ULN (unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin)
  • Calculated creatinine clearance > 45 mL/min by the Cockcroft-Gault equation.
  • Treating investigator must specify at screening:

    • If the intent of therapy is a bridge to cellular therapy or to complete all six cycles of therapy. If bridge to cellular therapy is planned, the type of cellular therapy should also be specified at this time.
    • If the r/r CNS lymphoma is primary or secondary
  • For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use two methods of contraception simultaneously from signing the ICF, at least 28 days before starting golcadomide, throughout the study, for up to 28 days following the last dose of golcadomide, and for 12 months after the last dose of rituximab, whichever is longer.. Two methods of contraception must include one highly effective method and one additional effective (barrier method).

    • A woman is considered to be of childbearing potential if she is postmenarcheal, has not reached a postmenopausal state (< 12 continuous months of amenorrhea with no identified cause other than menopause), and has not undergone surgical sterilization (removal of ovaries, fallopian tubes, and/or uterus).

      • Examples of contraceptive methods include highly effective methods such as oral, injectable, or implantable hormonal contraceptive; tubal ligation; intrauterine device; vasectomized partner and barrier methods with spermicide.
      • The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception.
      • Must agree to pregnancy testing per protocol. This applies even if the participant practices true abstinence from heterosexual contact.
      • Agree to abstain from breastfeeding or providing breast milk while on golcadomide and 28 days after discontinuation of golcadomide and according to the approved
    • For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures, and agreement to refrain from donating sperm, as defined below:
    • With female partners of childbearing potential, men must remain abstinent or use a condom plus an additional contraceptive method that together result in a failure rate of < 1% per year during the treatment period and for at least 28 days after the last dose of study intervention or 90 days for rituximab, whichever is longer. Men must refrain from donating sperm during this same period.
    • With pregnant female partners, men must remain abstinent or use a condom during the treatment period and for at least 28 days after the last dose of study intervention or 90 days for rituximab, whichever is longer.
    • The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception.

Exclusion Criteria:

  • Prior treatment toxicities not resolved to grade < 2 according to NCI CTCAE 6.0 (with the exception of alopecia or grade 2 sensory peripheral neuropathy).
  • Participants receiving any other investigational agents.
  • History of anaphylactic reactions or severe allergic reactions prohibiting further administration attributed to compounds of similar chemical or biologic composition to rituximab or other agents used in this study.
  • Autologous stem cell transplant within 30 days of start of study drug (C1D1).
  • CAR T-cell therapy within 90 days of start of study drug (C1D1).
  • Previous allogeneic stem cell transplant
  • Women who are pregnant or breastfeeding.
  • Clinically significant autoimmune disease.
  • Known seropositive and requiring anti-viral therapy for human immunodeficiency (HIV) virus.
  • Malabsorption syndrome or other conditions that precludes enteral route of administration.
  • Chemotherapy or radiation within 2 weeks of the first scheduled study treatment
  • Participant is currently receiving warfarin. Participants may begin screening if the plan is to change to an alternative anticoagulant such as a DOAC prior to enrollment.
  • Participant has current treatment with strong cytochrome P450 3A4/5 (CYP3A4/5) modulators. The washout period for strong CYP3A4/5 modulators is 7 days or 5 half-lives (whichever is longer) before initiation of golcadomide.
  • Evidence of other clinically significant uncontrolled condition(s) including, but not limited to:

    • Uncontrolled and/or active systemic infection (viral, bacterial or fungal)
    • Chronic hepatitis B virus (HBV) or hepatitis C (HCV) requiring treatment. Note: participants with serologic evidence of prior vaccination to HBV (i.e. hepatitis B surface (HBs) antigen negative-, anti-HBs antibody positive and anti-hepatitis B core (HBc) antibody negative) or positive anti-HBc antibody from intravenous immunoglobulins (IVIG) may participate.
    • Other uncontrolled conditions including uncontrolled cardiovascular disease or arrhythmia, decompensated diabetes or COPD.

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: Golcadomide + Pemetrexed, Rituximab and Dexamethasone
A 3+3 design will be used to identify the recommended phase 2 dose of Golcadomide in combination with Pemetrexed, Rituximab, and Dexamethasone. 3 participants will be enrolled in the first dose level. If these participants do not experience any dose limiting toxicities, then 3 more patients will be enrolled in the next dose level. If one or more participants experience dose limiting toxicities, then this dose will be considered the highest dose administered dose and 3 additional patients will be enrolled in the next lowest dose level. If 2 or more patients experience dose limiting toxicities, then the dose escalation will be stopped and 3 additional patients will enrolled in the next lowest dose level.

To be taken orally daily on days 1-7 of the cycle

Maximum 3 cycles but participants may received up to 3 additional cycles (for a total of up to 6 cycles)

Cycle Length : 21 days

Dose Levels:

  • Level -1 : 0.2milligrams/day
  • Level 1 : 0.2milligrams/day
  • Level 2 : 0.4milligrams/day

To be given intravenously (IV) on day 1 of each cycle

Maximum 3 cycles but participants may receive up to 3 additional cycles (for a total of up to 6 cycles)

Cycle Length: 21 days

Dose Level

  • Level -1 : 675 milligrams/square meter
  • Level 1 : 900 milligrams/square meter
  • Level 2 : 900 milligram/square meter

To be given intravenously on day 1 of each cycle

Maximum 3 cycles but participants may receive up to 3 additional cycles (for a total of up to 6 cycles)

Cycle Length: 21 days

Dose Level

  • Level -1 : 500 milligram/ square meter
  • Level 1 : 500 milligram/ square meter
  • Level 2 : 500 milligram/ square meter

To be given orally on days 1-4 of each cycle

Day 1 dose should be given at least 30 minutes before rituximab infusion

Maximum 3 cycles but participants may receive up to 3 additional cycles (for a total of up to 6 cycles)

Cycle Length: 21 days

Dose Level

  • Level -1 : 10 milligrams
  • Level 1 : 10 milligrams
  • Level 2 : 10 milligrams

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Safety of Golcadomide + Pemetrexed, Rituximab and Dexamethasone
Periodo de tiempo: up to 6 cycles (up to 6 months)
Safety is defined as rates of adverse events experienced by participants. Adverse event severity is graded according to the NCI Common Terminology Criteria for Adverse Events (CTCAE), Version 6.0.
up to 6 cycles (up to 6 months)
Identify the maximum tolerated dose of Golcadomide + Pemetrexed, Rituximab and Dexamethasone
Periodo de tiempo: up to 6 cycles (up to 6 months)
determined by the 3+3 dose escalation design
up to 6 cycles (up to 6 months)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall response rate (ORR) by International Primary CNS Lymphoma Collaborative Group (IPCG) of Golca + PRD
Periodo de tiempo: up to 18 months

ORR includes complete response (CR), Unconfirmed CR (CRu), partial response (PR), & disease control rate (DCR), according to the 2005 IPCG Response Criteria.

CR: complete disappearance of abnormalities on gadolinium-enhanced MRI, no contrast enhancement in brain imaging, no corticosteroid dose, normal eye examination & negative Cerebrospinal fluid (CSF) cytology.

CRu: fulfilling criteria for CR but with minimum to no contrast enhancement in brain imaging, continuing use of corticosteroid therapy, normal to minor retinal pigment epithelium (RPE) abnormality, & negative CSF cytology.

PR: greater than 50% decrease in contrast-enhancing lesion compared to baseline imaging, normal to minor RPE abnormality, negative CSF cytology & no new sites of disease.

SD: less than a PR but is not progressive disease.

up to 18 months
Disease control rate (DCR) by IPCG
Periodo de tiempo: 18 months

DCR is the percentage of participants whose cancer did not get worse after treatment (i.e. the percentage of participants who had CR, PR, or , SD, as defined below), and this will be measured by the IPCG response criteria.

CR: complete disappearance of abnormalities on gadolinium-enhanced MRI, no contrast enhancement in brain imaging, no corticosteroid dose, normal eye examination & negative Cerebrospinal fluid (CSF) cytology.

CRu: fulfilling criteria for CR but with minimum to no contrast enhancement in brain imaging, continuing use of corticosteroid therapy, normal to minor retinal pigment epithelium (RPE) abnormality, & negative CSF cytology.

PR: greater than 50% decrease in contrast-enhancing lesion compared to baseline imaging, normal to minor RPE abnormality, negative CSF cytology & no new sites of disease.

SD: less than a PR but is not progressive disease.

18 months
Overall survival rate
Periodo de tiempo: 18 months
Overall survival (OS) is defined as the duration of time from start of treatment to time of death from any cause for participants who complete treatment.
18 months
Progression free survival rate
Periodo de tiempo: 18 months
Progression-Free Survival (PFS) is defined as the duration of time from start of treatment to time of progression or death, whichever occurs first, for participants who complete treatment.
18 months
Proportion of participants designated for cellular therapy who receive cellular therapy
Periodo de tiempo: 18 months
The number of participants intended for cellular therapy who receive cellular therapy will be described as a proportion.
18 months
Proportion of participants who have a successful mobilization of autologous stem cell transplant
Periodo de tiempo: 18 months
The number of participants who undergo mobilization for collection of autologous stem cell transplant following treatment with Golca + RPD and have successful mobilization will be described as proportion.
18 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: Allison M Winter, MD, Cleveland Clinic, Case Comprehensive Cancer Center

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)

1 de octubre de 2026

Finalización primaria (Estimado)

1 de abril de 2029

Finalización del estudio (Estimado)

1 de septiembre de 2029

Fechas de registro del estudio

Enviado por primera vez

20 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

20 de mayo de 2026

Publicado por primera vez (Actual)

27 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

21 de agosto de 2026

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

19 de agosto de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

Descripción del plan IPD

All IPD that underlie results in publication will be shared with the FDA, UH, and Bristol Myers Squibb, who are the suppliers of the investigational product. Any patient data shared will be deidentified.

Marco de tiempo para compartir IPD

Data included in the peer-reviewed publication will be publicly available indefinitely. No raw data will be shared.

Criterios de acceso compartido de IPD

A peer-reviewed publication will be made available according to the publishing journal's specifications. CCF personal will not share study data apart that which has been published publicly.

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • CIF
  • RSC

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.

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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