跳至主要内容
临床试验/NL-OMON29878
NL-OMON29878尚未招募3 期

A double-blind, randomized, two-dose-arm, parallel group, international, multi-center trial of HuMax-CD20, a fully human monoclonal anti-CD20 antibody, in patients with Follicular Lymphoma who are refractory to rituximab in combination with chemotherapy - HuMax-CD20 in FL patients refractory to rituximab

Genmab0 个研究点目标入组 9 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
Genmab
入组人数
9

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • diagnosis of Follicular Lymphoma grade 1* 2 refractory to rituximab in combination with chemotherapy or to rituximab given as maintenance treatment

排除标准

  • The most important exclusion criteria consist of allogenic stem cell transplantation at any time, autologous stem cell transplantation within 6 months prior to Visit 1, more than 1 previous cycle of radio immunotherapy, anticancer therapy or corticosteroid therapy within 4 weeks prior to Visit 1 or known or suspected transformation of the follicular lymphoma to aggressive lymphoma unless new biopsy confirms FL.

研究者

发起方
Genmab

相似试验

进行中(未招募)
不适用
A double-blind, randomized, two-dose-arm, parallel group, international, multi-center trial of HuMax-CD20, a fully human monoclonal anti-CD20 antibody, in patients with Follicular Lymphoma who are refractory to rituximab as monotherapy or in combination with chemotherapy - HuMax-CD20 in FL patients refractory to rituximabon-Hodgkin Follicular LymphomaClassification code 10003899
EUCTR2006-001433-17-DKGenmab A/S162
进行中(未招募)
不适用
A double-blind, randomized, two-dose-arm, parallel, international, multi-center trial of HuMax-CD20, a fully human monoclonal anti-CD20 antibody, in patients with Follicular Lymphoma who are refractory to rituximab in combination with chemotherapy - HuMax-CD20 in FL patients refractory to rituximabFollicular LimphomaMedDRA version: 14.1Level: HLGTClassification code 10025320Term: Lymphomas non-Hodgkin's B-cellSystem Organ Class: 10005329 - Blood and lymphatic system disorders
EUCTR2006-001433-17-ITGLAXO SMITH KLINE RESEARCH & DEVELOPMENT LTD161
进行中(未招募)
不适用
A double-blind, randomized, two-dose-arm, parallel group, international, multi-center trial of HuMax-CD20, a fully human monoclonal anti-CD20 antibody, in patients with Follicular Lymphoma who are refractory to rituximab as monotherapy or in combination with chemotherapy - HuMax-CD20 in FL patients refractory to rituximab
EUCTR2006-001433-17-DEGlaxo SmithKline Research and Development Limited120
进行中(未招募)
不适用
A double-blind, randomized, two-dose-arm, parallel group, international, multi-center trial of HuMax-CD20, a fully human monoclonal anti-CD20 antibody, in patients with Follicular Lymphoma who are refractory to rituximab in combination with chemotherapy - HuMax-CD20 in FL patients refractory to rituximabon-Hodgkin Follicular LymphomaMedDRA version: 8.1Level: PTClassification code 10003899Term: B-cell lymphoma
EUCTR2006-001433-17-NLGenmab A/S162
进行中(未招募)
不适用
Bioequivalence study with clinical endpoint in the treatment of subjects with chronic open-angle glaucoma or ocular hypertension in both eyes.
CTRI/2022/04/042203Amneal EU Limited