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临床试验/NCT07094048
NCT07094048招募中4 期

Immunoglobulins in Multiple Myeloma Patients Receiving a BCMA-Directed T Cell Engager

CHU de Quebec-Universite Laval3 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年1月5日最近更新:
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
80
试验地点
3
主要终点
Severe infections

研究概览

简要总结

Bispecific antibody therapies targeting BCMA (B-cell maturation antigen) represent a novel therapeutic approach for patients with multiple myeloma. They are currently used in cases of refractory multiple myeloma but are also being investigated in earlier lines of treatment. However, these new therapies can lead to deeper immunosuppression and exacerbate an underlying immunosuppressive state in patients with multiple myeloma. As a result, infectious complications are common with these therapies and are a significant concern. Therefore, preventing infections in this population is crucial. However, data on the best strategies for prevention are currently lacking.

详细描述

Although the effectiveness of immunoglobulins (Ig) has been demonstrated, it remains to be determined whether immunoglobulin administration is necessary for all patients receiving these therapies or only for those with low serum immunoglobulin G (IgG) levels. Furthermore, the optimal target IgG level to achieve in order to reduce the risk of infections is also unknown in this specific population of multiple myeloma patients. Guidance needs to be provided to the clinicians to better support MM patients undergoing this novel therapy by addressing the hypogammaglobulinemia and therefore limiting and ideally avoiding the high risk of infections.

In this prospective, randomized, unblinded, multicenter study, as per the standard of care approach, every patient with relapsed refractory MM receiving a BCMA-directed TCE with history of recurrent or severe infections and/or total IgG level less than 4 g/L will receive Ig support (intravenous ou subcutaneous). Once on Ig supplementation, the optimal target trough IgG level to achieve is not well established. The goal of this study is therefore to better define, in this patient population , the target trough IgG level to achieve a reduction in the incidence of severe infections.

The primary objective is to demonstrate the non-inferiority in the cumulative incidence of severe infections at 3 months between patients on Ig support with a target trough IgG level of 4-6 g/L (experimental group) versus a target trough IgG level of 8-10 g/L (standard of care (SOC) group).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • Multiple myeloma patient:
  • ≥ 18 years old
  • ≥ 1 prior lines of therapy
  • Receiving a BCMA-directed T-cell Engager therapy (starting on treatment)
  • On previous Ig support or not

排除标准

  • Less than 18 years old
  • Pregancy or breastfeeding

研究组 & 干预措施

Group A IgG level 8-10 g/L

Active Comparator

Immunoglobulin support (subcutaneous or intravenous)

干预措施: Target trough IgG level of 8-10 g/L (Drug)

Group B IgG level 4-6 g/L

Experimental

Immunglobulin support (subcutaneous or intravenous)

干预措施: Target trough IgG level 4-6 g/L (Drug)

Group C

Other

No immunoglobulin support. If pre specified conditions are met, crossover to Group A or B.

干预措施: No history of recurrent or severe infections and total IgG level higher or equal at 4 g/L (Drug)

结局指标

主要结局

Severe infections

时间窗: From enrollment to 3 months after time of randomization

Non-inferiority in the cumulative incidence of severe infections at 3 months between patients on Ig support with a target trough IgG level of 4-6 g/L (experimental group) versus a target trough IgG level of 8-10 g/L (standard of care group)

次要结局

  • All infection rate(From enrollment to 12 months after randomization)
  • Minor/Moderate infections rate(From enrollment to 12 monts after randomization)

研究者

发起方
CHU de Quebec-Universite Laval
申办方类型
Other
责任方
Sponsor

研究点 (3)

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