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临床试验/EUCTR2020-000845-15-FI
EUCTR2020-000845-15-FI进行中(未招募)1 期

A Phase 1b/2, Open-Label Trial to Assess the Safety and Preliminary Efficacy of Epcoritamab (GEN3013; DuoBody®-CD3xCD20) in Combination with Other Agents in Subjects with B-cell Non-Hodgkin Lymphoma - EPCORE™ NHL-2

Genmab A/S0 个研究点目标入组 662 人开始时间: 2020年11月10日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Genmab A/S
入组人数
662

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1.Subject must sign an ICF
  • 2.At least 18 years of age
  • 3.Measurable disease defined as =1 measurable nodal lesion (long axis >1.5 cm and short axis >1.0 cm) or =1 measurable extra-nodal lesion (long axis >1.0 cm) on CT or MRI
  • 4.ECOG PS score of 0, 1 or 2
  • 5.Acceptable organ function at screening
  • 6.CD20-positive NHL at most recent representative tumor biopsy
  • 7.If of childbearing potential subject must practicing a highly effective method of birth control
  • 8.A man who is sexually active with a woman of childbearing potential must agree to use a barrier method of birth control
  • 9.Life expectancy >2 months with SOC treatment.
  • Arm 1: One of these confirmed histologies:
  • -DLBCL, NOS
  • - T-cell/histiocyte rich DLBCL
  • -double-hit or triple-hit DLBCL
  • -FL Grade 3B
  • Arm 2 and Arm 9: R/R FL
  • Arm 3: Newly diagnosed, previously untreated FL grade 1-3A
  • Arm 4 and Arm 10: One of these confirmed histologies and eligible for HDT-ASCT
  • -DLBCL, NOS
  • - - T-cell/histiocyte rich DLBCL
  • -double-hit or triple-hit DLBCL
  • -FL Grade 3B
  • Arm 5: One of these confirmed histologies and ineligible for HDT-ASCT
  • -DLBCL, NOS
  • - T-cell/histiocyte rich DLBCL
  • -double-hit or triple-hit DLBCL
  • -FL Grade 3B
  • Arm 6: previously untreated CD20+ FL
  • Arm 7: FL and in CR or PR per Lugano criteria following first-line or second-line treatment with SOC regiment and last dose of SOC within 6
  • months prior to enrollment
  • Arm 8: One of these confirmed histologies:
  • - DLBCL, NOS
  • - T-cell/histiocyte rich DLBCL
  • - double-hit or triple-hit DLBCL
  • -FL Grade 3B
  • For Arm8, subjects must be ineligible to receive full-dose anthracycline
  • (as part of R-CHOP) per eligibility criteria
  • Arm 9: Must have received only 1 prior line of therapy. This first-line therapy must have included an anti-CD20 antibody in combination with chemotherapy. Progressed within 24 months of initiating first-line treatment
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 331
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 331

排除标准

  • 1.Chemotherapy, radiation therapy, or major surgery within 4 weeks prior to the first dose of epcoritamab
  • 2.Any prior treatment with a bispecific antibody targeting CD3 and CD20.
  • 3.Treatment with CAR-T therapy within 100 days prior to first dose of epcoritamab
  • 4.Clinically significant cardiovascular disease
  • 5.Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results
  • 6.CNS lymphoma or known CNS involvement by lymphoma at screening as confirmed by MRI/CT scan of the brain and, if clinically indicated, by lumbar puncture
  • 7.Active HBV or HBC (DNA PCR positive infection)
  • 8.Known history of seropositivity for human immunodeficiency virus
  • 9. Active tuberculosis or history of completed treatment for active
  • tuberculosis within the past 12 months
  • 10. Subject has current seizure disorder requiring anti-epileptic therapy

研究者

发起方
Genmab A/S

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