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Rimegepant Plus Glofitamab and CD19 CAR-T Therapy in R/R LBCL

23. maj 2026 opdateret af: Zhao Weili, Ruijin Hospital

A Study to Evaluate the Efficacy and Safety of Rimegepant Plus Glofitamab and CD19 CAR-T Cell Therapy in Patients With High-Risk Relapsed/Refractory Large B-Cell Lymphoma

This study is designed to evaluate the efficacy and safety of rimegepant in combination with glofitamab and CD19 CAR-T cell therapy in patients with high-risk relapsed/refractory large B-cell lymphoma. Eligible patients will be randomized to receive glofitamab plus CD19 CAR-T cell therapy with or without rimegepant. The primary endpoint is complete response rate at 6 months after CAR-T cell infusion.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

100

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

  • Navn: Weili Zhao
  • Telefonnummer: +862164370045 Ext. 610707
  • E-mail: zwl_trial@163.com

Undersøgelse Kontakt Backup

Studiesteder

    • China
      • Shanghai, China, Kina, 200020
        • Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Able to understand and voluntarily sign the written informed consent form.
  • Age 18 years or older.
  • Histologically confirmed large B-cell lymphoma with CD19 and CD20 expression.
  • Relapsed or refractory disease after at least one prior line of systemic therapy.
  • Prior treatment must have included an anthracycline-containing chemotherapy regimen and an anti-CD20 monoclonal antibody.
  • Considered suitable by the investigator to receive glofitamab and CD19 CAR-T cell therapy.
  • Presence of at least one high-risk feature, including extranodal involvement, bulky disease, or TP53 abnormality.
  • ECOG performance status of 0 to 2.
  • Life expectancy of at least 12 weeks.
  • Adequate bone marrow, hepatic, renal, pulmonary, and cardiac function as determined by the investigator.
  • Participants of reproductive potential must agree to use effective contraception during the study period.
  • Able and willing to comply with the study protocol, in the investigator's judgment.

Exclusion Criteria:

  • History of hypersensitivity to any study treatment or related compounds.
  • Active or uncontrolled infection requiring systemic treatment.
  • History of allogeneic hematopoietic stem cell transplantation or organ transplantation.
  • Uncontrolled or clinically significant viral infection as defined by the protocol.
  • Known central nervous system involvement by lymphoma or clinically significant central nervous system disease that may interfere with study treatment or safety assessment.
  • Severe or uncontrolled cardiovascular disease.
  • Severe autoimmune disease or immune-mediated disease that may interfere with study treatment or safety assessment.
  • Known or suspected history of hemophagocytic lymphohistiocytosis.
  • Recent thromboembolic event before screening.
  • History of another malignancy within 5 years before screening, except adequately treated carcinoma in situ or non-melanoma skin cancer.
  • Receipt of prohibited anticancer therapy, immunosuppressive therapy, live attenuated vaccine, or other prohibited treatment within the protocol-specified period before enrollment.
  • Pregnant or breastfeeding women, or participants planning pregnancy during the study period.
  • Concurrent participation in another interventional clinical trial.
  • Need for prohibited concomitant medications that cannot be discontinued or substituted.
  • Any condition that, in the investigator's judgment, makes the participant unsuitable for study treatment or study participation.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Rimegepant Plus Glofitamab and CD19 CAR-T Cell Therapy
Participants will receive rimegepant in combination with glofitamab and CD19 CAR-T cell therapy. Rimegepant will be administered orally at 75 mg every other day from the first day of lymphodepleting chemotherapy until Day 90 after CAR-T cell infusion. Glofitamab will be given with obinutuzumab pretreatment and step-up dosing, followed by CD19 CAR-T cell therapy after lymphodepleting chemotherapy. Participants with CR, PR, or SD after CAR-T cell infusion may continue glofitamab consolidation according to the study protocol.
Rimegepant will be administered orally at 75 mg every other day from the first day of lymphodepleting chemotherapy until Day 90 after CAR-T cell infusion.
Glofitamab will be administered intravenously with step-up dosing. Participants will receive 2.5 mg on Cycle 1 Day 8, 10 mg on Cycle 1 Day 15, and 30 mg on Cycle 2 Day 1. Participants with CR, PR, or SD after CAR-T cell infusion may continue glofitamab consolidation at 30 mg on Day 1 of each 21-day cycle for four cycles.
Obinutuzumab will be administered intravenously at 1000 mg on Cycle 1 Day 1 as pretreatment before glofitamab.
Participants will receive CD19-directed CAR-T cell therapy after lymphodepleting chemotherapy. The specific CAR-T product and dose will be determined according to the approved product label, institutional standard practice, and investigator discretion.
Fludarabine will be administered as part of lymphodepleting chemotherapy before CD19 CAR-T cell infusion.
Cyclophosphamide will be administered as part of lymphodepleting chemotherapy before CD19 CAR-T cell infusion.
Aktiv komparator: Glofitamab Plus CD19 CAR-T Cell Therapy
Participants will receive glofitamab in combination with CD19 CAR-T cell therapy. Glofitamab will be given with obinutuzumab pretreatment and step-up dosing, followed by CD19 CAR-T cell therapy after lymphodepleting chemotherapy. Participants with CR, PR, or SD after CAR-T cell infusion may continue glofitamab consolidation according to the study protocol.
Glofitamab will be administered intravenously with step-up dosing. Participants will receive 2.5 mg on Cycle 1 Day 8, 10 mg on Cycle 1 Day 15, and 30 mg on Cycle 2 Day 1. Participants with CR, PR, or SD after CAR-T cell infusion may continue glofitamab consolidation at 30 mg on Day 1 of each 21-day cycle for four cycles.
Obinutuzumab will be administered intravenously at 1000 mg on Cycle 1 Day 1 as pretreatment before glofitamab.
Participants will receive CD19-directed CAR-T cell therapy after lymphodepleting chemotherapy. The specific CAR-T product and dose will be determined according to the approved product label, institutional standard practice, and investigator discretion.
Fludarabine will be administered as part of lymphodepleting chemotherapy before CD19 CAR-T cell infusion.
Cyclophosphamide will be administered as part of lymphodepleting chemotherapy before CD19 CAR-T cell infusion.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Complete Response Rate at 6 Months
Tidsramme: 6 months after CAR-T cell infusion
Complete response rate at 6 months is defined as the proportion of participants who achieve complete response at 6 months after CAR-T cell infusion.
6 months after CAR-T cell infusion

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Objective Response Rate
Tidsramme: Up to 24 months
Objective response rate is defined as the proportion of participants who achieve complete response or partial response.
Up to 24 months
Complete Response Rate at Day 28
Tidsramme: Day 28 after CAR-T cell infusion
Complete response rate at Day 28 is defined as the proportion of participants who achieve complete response at Day 28 after CAR-T cell infusion.
Day 28 after CAR-T cell infusion
Complete Response Rate at 3 Months
Tidsramme: 3 months after CAR-T cell infusion
Complete response rate at 3 months is defined as the proportion of participants who achieve complete response at 3 months after CAR-T cell infusion.
3 months after CAR-T cell infusion
Progression-Free Survival
Tidsramme: Up to 24 months
Progression-free survival is defined as the time from randomization to disease progression or death from any cause, whichever occurs first.
Up to 24 months
Duration of Response
Tidsramme: Up to 24 months
Duration of response is defined as the time from the first documented response to disease progression or death from any cause, whichever occurs first.
Up to 24 months
Overall Survival
Tidsramme: Up to 24 months
Overall survival is defined as the time from randomization to death from any cause.
Up to 24 months
Adverse Events
Tidsramme: Up to 24 months
Incidence and severity of adverse events will be assessed throughout the study.
Up to 24 months

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. maj 2026

Primær færdiggørelse (Anslået)

1. november 2028

Studieafslutning (Anslået)

1. april 2029

Datoer for studieregistrering

Først indsendt

23. maj 2026

Først indsendt, der opfyldte QC-kriterier

23. maj 2026

Først opslået (Faktiske)

29. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

29. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. maj 2026

Sidst verificeret

1. maj 2026

Mere information

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