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NCT04205838Leállítva2. fázis

Anakinra in Preventing Severe Chimeric Antigen Receptor T-Cell Related Encephalopathy Syndrome in Patients With Recurrent or Refractory Large B-cell Lymphoma

IL-1 Receptor Antagonist to Prevent Severe Chimeric Antigen Receptor T-Cell Related Encephalopathy Syndrome

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. febr. 27.

Megadott ok: slow accrual

Rövid összefoglaló (regiszter, angolul)

This phase II trial studies how well anakinra works in preventing severe chimeric antigen receptor T-cell-related encephalopathy syndrome after chimeric antigen receptor T-cell therapy in patients with large B-cell lymphoma that has come back or has not responded to treatment. Immunosuppressive therapy, such as anakinra, is used to decrease the body?s immune response, which may prevent severe chimeric antigen receptor T-cell-related encephalopathy syndrome.

Állapot (regiszter)
Leállítva
Fázis (regiszter)
2. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
23 (tényleges)
Első benyújtás
2019. okt. 2.
Kezdés
2020. márc. 4.
Elsődleges befejezés
2026. febr. 19.
Fő szponzor
Jonsson Comprehensive Cancer Center
NCT-szám
NCT04205838

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Korábbi kezelés

  • Patients who receive CAR T-cell therapy with a product other than axicabtagene ciloleucel
  • Bridging chemotherapy completed < 7 days prior to CAR T-cell lymphodepleting chemotherapy
  • In patients who receive bridging chemotherapy, positron emission tomography (PET)-computed tomography (CT) or CT of chest, abdomen, pelvis was not done after bridging chemotherapy prior lympho-depleting therapy
  • Most recent PET-CT or CT of all known disease is sites done more than 6 weeks prior to CAR T-cell infusion
  • History of autologous hematopoietic stem cell transplantation administered less than 100 days prior to CAR T-cell infusion
  • Treatment with alemtuzumab within 6 months prior to leukapheresis, or treatment with clofarabine or cladribine within 3 months prior to leukapheresis
  • Less than 3 half-lives elapsed since receiving immune checkpoint inhibitor (pembrolizumab, ipilimumab, nivolumab, atezolizumab, etc.)

Más betegség

  • History of allogeneic hematopoietic stem cell transplantation
  • Presence of uncontrolled fungal, bacterial, or viral infection that require intravenous (IV) antimicrobial treatment
  • History of autoimmune disease resulting in end-organ damage, or autoimmune disease requiring systemic immunosuppressants or disease-modifying antirheumatic drug (DMARDs) within the past 6 months
  • Hypersensitivity to E. Coli-derived proteins
  • Patients with HIV who have a detectable viral load

Egyéb

  • Primary CNS lymphoma
  • Transformed DLBCL from chronic lymphocytic leukemia (CLL)
  • Burkitt?s lymphoma
  • Any individual CNS tumor mass > 2 cm
  • Pregnant or nursing
  • Fertile women who decline use of contraception during the study period

Kiket keres a vizsgálat

  • Patients with relapsed or refractory large B-cell lymphoma that has progressed on two prior lines of therapy, who meet the indication for the Food and Drug Administration (FDA)-approved therapy axicabtagene ciloleucel
  • Large B-cell lymphoma includes diffuse large B-cell lymphoma (DLBCL) not otherwise specified, primary mediastinal large B-cell lymphoma, high grade B-cell lymphoma, and DLBCL arising from follicular lymphoma
  • The above includes patients with progressive or stable disease as the best response to the most recent treatment regimen or disease progression within 12 months after autologous hematopoietic stem cell transplantation
  • Patients with central nervous system (CNS) involvement of large B-cell lymphoma that originated outside of the CNS will be included (not primary CNS lymphoma)
  • Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) =< 2.5 upper limit of normal
  • Total bilirubin =< 2.0 mg/dL
  • Creatinine clearance > 30 mL/min based on Cockcroft-Gault formula
  • Patients with human immunodeficiency virus (HIV) who have an undetectable viral load will be included
  • Deemed competent to make medical decisions

Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (2)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
UC Davis Comprehensive Cancer CenterDavisEgyesült ÁllamokIsmeretlen állapot
UCLA / Jonsson Comprehensive Cancer CenterLos AngelesEgyesült ÁllamokIsmeretlen állapot

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