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

Not Applicable

Not yet recruiting

• Conditions: Multiple Myeloma Refractory; Relapsed Multiple Myeloma
• Interventions: Drug: Target trough IgG level of 8-10 g/L; Drug: Target trough IgG level 4-6 g/L; Drug: No history of recurrent or severe infections and total IgG level higher or equal at 4 g/L

• Registration Number: NCT07094048
• Lead Sponsor: CHU de Quebec-Universite Laval

Brief Summary

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.

Detailed Description

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).

Study Timeline

• Status Verified: 2025-07
• Study First Submitted: 2025-07-11
• Study First Submitted QC: 2025-07-28
• Last Update Submitted: 2025-07-28
• Study First Posted: 2025-07-30
• Last Update Posted: 2025-07-30
• Study Start: 2025-09-01
• Primary Completion: 2028-12
• Study Completion: 2029-12-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

• 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

Exclusion Criteria

• Less than 18 years old
• Pregancy or breastfeeding

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group A IgG level 8-10 g/L	Target trough IgG level of 8-10 g/L	Immunoglobulin support (subcutaneous or intravenous)
Group B IgG level 4-6 g/L	Target trough IgG level 4-6 g/L	Immunglobulin support (subcutaneous or intravenous)
Group C	No history of recurrent or severe infections and total IgG level higher or equal at 4 g/L	No immunoglobulin support. If pre specified conditions are met, crossover to Group A or B.

Primary Outcome Measures

Name	Time	Method
Severe infections	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)

Secondary Outcome Measures

Name	Time	Method
All infection rate	From enrollment to 12 months after randomization	All infections rate
Minor/Moderate infections rate	From enrollment to 12 monts after randomization	Rates of minor/moderate infection rates

Trial Locations

Locations (1)

Centre Intégré de Cancérologie; 🇨🇦 Québec, Quebec, Canada