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

2026年8月19日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (推定)

18

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Allison M Winter, MD
  • 電話番号:(216) 445-4635
  • メール:wintera2@ccf.org

研究場所

    • Ohio
      • Cleveland、Ohio、アメリカ、44122
        • Cleveland Clinic, Case Comprehensive Cancer Center
        • 主任研究者:
          • Allison Winter, MD
        • コンタクト:
          • Allison M Winter, MD
          • 電話番号:(216) 445-4635
          • メール:wintera2@ccf.org

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Safety of Golcadomide + Pemetrexed, Rituximab and Dexamethasone
時間枠: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
時間枠:up to 6 cycles (up to 6 months)
determined by the 3+3 dose escalation design
up to 6 cycles (up to 6 months)

二次結果の測定

結果測定
メジャーの説明
時間枠
Overall response rate (ORR) by International Primary CNS Lymphoma Collaborative Group (IPCG) of Golca + PRD
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Allison M Winter, MD、Cleveland Clinic, Case Comprehensive Cancer Center

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年10月1日

一次修了 (推定)

2029年4月1日

研究の完了 (推定)

2029年9月1日

試験登録日

最初に提出

2026年5月20日

QC基準を満たした最初の提出物

2026年5月20日

最初の投稿 (実際)

2026年5月27日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月21日

QC基準を満たした最後の更新が送信されました

2026年8月19日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

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.

IPD 共有時間枠

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

IPD 共有アクセス基準

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.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

はい

米国FDA規制機器製品の研究

いいえ

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