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
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
- 否
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
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
