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临床试验/NCT02252146
NCT02252146已完成1 期

Phase I/II Open-label, Multiple-dose, Dose-escalation Study to Evaluate the Safety and Tolerability of IMO-8400 in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma and Presence of the MyD88 L265P Mutation

Idera Pharmaceuticals, Inc.12 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2014年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
6
试验地点
12
主要终点
Number of Participants With Adverse Events, Injection Site Reactions, and Concomitant Medications

研究概览

简要总结

Recent reports have identified a specific oncogenic mutation L265P of the MYD88 gene in approximately 30% of the patients with the activated B-cell (ABC) type of Diffuse Large B Cell Lymphoma (DLBCL). MYD88 is an initial adapter linker protein in the signaling pathway of the Toll Like Receptors (TLRs), including the endosomal TLRs 7, 8, and 9, for which the ligands are nucleic acids. IMO-8400 is an oligonucleotide specifically designed to inhibit ligand activation of TLRs 7,8, and 9. Recent studies indicate that in the presence of L265P mutation ligand activation of those TLRs results in markedly increased signaling with subsequent increased cell activation, cell survival, and cell proliferation. The scientific rationale for assessing the use of IMO-8400 to treat patients with DLBCL and the L265P mutation is based on laboratory observations that IMO-8400 inhibits ligand-based activation of cells with the mutation and decreases the survival and proliferation of the cell populations responsible for the propagation of the disease.

详细描述

Eligible subjects will be enrolled and assigned to one of five dose cohorts. Treatment will be administered by subcutaneous injection until progression or intolerable toxicity.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must have a diagnosis of Diffuse Large B Cell Lymphoma (DLBCL) of non-GCB subtype, established according to the World Health Organization (WHO) criteria that has been tested for the MyD88 L265P mutation.
  • In addition to the above, key inclusion and exclusion criteria are listed below.
  • Be at least 18 years of age
  • Agree to use contraception

排除标准

  • Is nursing or pregnant
  • DLBCL of GCB subtype
  • Has BMI > 34.9 kg/m2
  • Has a positive test for human immunodeficiency virus (HIV-1 or -2) hepatitis C virus (HCV) or hepatitis B surface antigen (HBsAg)
  • Receiving chronic systemic corticosteroid therapy > 20 mg of prednisone daily
  • Being treated with other anti-cancer therapies (approved or investigational)
  • Has an active infection requiring systemic antibiotics
  • Has had surgery requiring general anesthesia within 4 weeks of starting the study
  • Has heart failure of Class III or IV

研究组 & 干预措施

IMO-8400

Experimental

IMO-8400 0.3 mg/kg twice weekly, 0.6 mg/kg twice weekly, or 1.2 mg/kg twice weekly

干预措施: IMO-8400 (Drug)

结局指标

主要结局

Number of Participants With Adverse Events, Injection Site Reactions, and Concomitant Medications

时间窗: Up to 2 years from first patient visit

Frequency of adverse events, injection site reactions, and concomitant medications observed

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (12)

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