An observational study in Myeloma Multiple, sponsored by The Royal Wolverhampton Hospitals NHS Trust. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-23.
Sponsored by The Royal Wolverhampton Hospitals NHS Trust · Observational
Elranatamab is an effective BCMA-targeting bispecific antibody for relapsed/refractory multiple myeloma (RRMM). However, implementation in routine practice remains challenging due to monitoring requirements during step-up dosing for cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS), together with the long-term burden of infection prevention and immunoglobulin replacement. Delivery models across the NHS vary considerably, including inpatient, ambulatory, outpatient, and virtual ward step-up dosing approaches. Supportive-care practice also evolved following NHS commissioning of primary immunoglobulin replacement for selected patients with hypogammaglobulinaemia.
This study will evaluate real-world implementation of elranatamab across the NHS to identify approaches to safe, scalable, and equitable delivery. Primary objectives are to evaluate acute delivery pathways for CRS/ICANS management during step-up dosing and long-term infection management, including immunoglobulin replacement. Secondary objectives include assessment of healthcare resource utilisation, treatment delivery patterns, infection outcomes, and clinical outcomes across diverse healthcare and socioeconomic settings.
The study population will be RRMM patients receiving elranatamab through NHS funding or compassionate access programmes from 01/01/2024 till 31/12/2026. Patients treated within clinical trials will be excluded.
This national multicentre retrospective observational study will utilise the UKCHART research network, with 20 participating tertiary and district general hospitals. Variation in delivery pathways, toxicity management strategies, and supportive-care practices, together with changes in NHS immunoglobulin replacement policy, has created a natural experiment in elranatamab implementation. Approximately 400 patients are anticipated. There will be two retrospective data collection sweeps. The first will capture baseline characteristics, treatment history, delivery pathways, toxicity management, infection prevention strategies, healthcare resource utilisation, and early outcomes. The second, conducted around 12 months later, will provide longer-term follow-up including infection outcomes, immunoglobulin replacement utilisation, treatment patterns, subsequent therapies, and cumulative resource utilisation.
Analyses will evaluate delivery models, CRS/ICANS management strategies, serious infections requiring hospitalisation, intensive care admission or death, immunoglobulin replacement utilisation, hospital admissions, bed-day utilisation, and variation across healthcare settings and socioeconomic groups.
This study will generate one of the largest national real-world datasets on elranatamab implementation. Findings will inform optimisation of monitoring strategies and supportive-care delivery including infection prevention, to guide evidence-based NHS delivery models for elranatamab and other T-cell redirecting therapies.
Elranatamab, a BCMA-targeting bispecific antibody, has emerged as an important treatment option in relapsed/refractory multiple myeloma, with clinically meaningful efficacy in patients with multiple prior lines of therapy. However, its clinical use is associated with a distinct toxicity profile, including cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), and an increased risk of infection. As a result, its implementation requires careful operational planning, particularly during step-up dosing and early-cycle monitoring.
Early clinical trial protocols were heavily influenced by CAR-T cell therapy pathways, with inpatient admission frequently used during step-up dosing to mitigate acute toxicity risk. While this approach prioritises safety, it places substantial demands on inpatient capacity and may not be feasible across all treatment centres. This creates potential inequities in access, particularly in hospitals with limited inpatient oncology infrastructure. In response, delivery models in routine clinical practice have evolved rapidly and now vary substantially, ranging from inpatient initiation to ambulatory day-case pathways and, increasingly, outpatient or hybrid virtual ward-based models. These differences largely reflect local infrastructure, service configuration, and institutional risk tolerance rather than a standardised, evidence-based framework.
Although uptake of elranatamab in clinical practice is increasing, there remains limited high-quality real-world evidence defining the optimal intensity of monitoring and care delivery required to ensure safe and efficient administration. In particular, uncertainty remains regarding the minimum level of monitoring that can be safely implemented without increasing clinically meaningful adverse outcomes, including severe CRS, unplanned hospitalisation, or early treatment discontinuation. This evidence gap has important implications for healthcare capacity and scalability, as more intensive inpatient-based approaches may substantially increase bed utilisation and limit equitable access within resource-constrained systems.
In parallel, approaches to infection prevention and immunoglobulin replacement therapy have evolved during the implementation of elranatamab in routine clinical practice. National practice has shifted from predominantly secondary immunoglobulin replacement strategies towards primary prophylaxis in selected patient groups, with current commissioning supporting immunoglobulin replacement in patients with IgG levels below 4 g/L, even in the absence of a significant infection history. This has resulted in routine, often indefinite immunoglobulin replacement during bispecific antibody therapy. While potentially reducing infection risk, this strategy introduces significant cost and treatment burden, effectively constituting dual long-term therapy with both a bispecific antibody and immunoglobulin replacement. Delivery approaches, including intravenous and subcutaneous administration, may also vary between centres, further contributing to heterogeneity in practice.
The clinical and economic impact of these evolving infection prevention strategies remains poorly defined, particularly in the context of sustained B-cell depletion and infection risk associated with BCMA-directed therapies. This represents an important evidence gap with respect to both patient outcomes and healthcare resource utilisation.
There is substantial variation in elranatamab delivery across routine clinical practice, encompassing tertiary and district general hospitals, differing models of ambulatory care provision, and emerging use of virtual ward infrastructure. This heterogeneity, combined with recent changes in immunoglobulin replacement policy, creates a natural experiment in which real-world implementation strategies and their consequences can be systematically evaluated at scale within a single healthcare system.
Taken together, there is a clear need for a national real-world evaluation to define evidence-based pathways for the safe, efficient, and equitable delivery of elranatamab in routine clinical practice. Specifically, there is a need to determine how different delivery models influence safety outcomes, healthcare resource utilisation, infection burden, and treatment continuity, and how evolving supportive care strategies, including immunoglobulin replacement, modify these outcomes. Addressing these gaps is essential to inform scalable implementation across diverse clinical settings while maintaining patient safety and ensuring equitable access to treatment.
The study population will be RRMM patients receiving elranatamab through NHS funding or compassionate access programmes from 01/01/2024 till 31/12/2026. Patients treated within clinical trials will be excluded.
It will be an Ambispective study with Retrospective and Prospective follow up.
3,712 studies on the registry are indexed under Multiple Myeloma; 752 are open to participants now.
This study's planned enrollment of 400 is above the median of 145 across 482 observational studies indexed under Multiple Myeloma.
Browse Multiple Myeloma studies →The Royal Wolverhampton Hospitals NHS Trust is the lead sponsor of 51 studies on the registry; 16 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Our targeted study population will be relapsed/refractory multiple myeloma patients
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Age ≥18 years.
Exclusion Criteria:
Incidence of early severe treatment-related toxicity during step-up dosing
Incidence of early severe treatment-related toxicity during step-up dosing, defined as: * Grade ≥3 CRS and/or ICANS, and/or * Unplanned hospital admission during step-up phase
Time frame: Time Period between 2024-2028
Incidence of serious infection during treatment
Incidence of serious infection during treatment, defined as: • Infection requiring hospital admission, ICU admission, or resulting in death
Time frame: Time Period between 2024-2028
Supportive care and infection-related management
• Utilisation of immunoglobulin replacement therapy (IVIG/SCIG), including initiation, duration, and treatment intensity
Time frame: Time Period between 2024-2028
Subgroup and implementation variation analyses
Associations between outcomes and: * Renal impairment * Prior BCMA-directed therapy exposure and refractoriness * Prior immunomodulatory (pomalidomide) refractoriness * Hospital type (tertiary centre vs district general hospital) * Socioeconomic deprivation index * Age and frailty (using simplified IMWG frailty score) * Ethnicity * Subsequent lines of therapy, including use of other bispecific antibodies
Time frame: Time Period between 2024-2028
Disease response and survival outcomes
a. Overall Response Rate (ORR) • Proportion of participants achieving a partial response or better, including VGPR and complete response (CR), according to standard disease response criteria.
Time frame: Time Period between 2024-2028
Disease response and survival outcomes
b: Progression-Free Survival (PFS) • Time from initiation of treatment to disease progression or death from any cause.
Time frame: Time Period between 2024-2028
Disease response and survival outcomes
c: Progression-Free Survival 2 (PFS2) • Time from initiation of treatment to second disease progression or death from any cause.
Time frame: Time Period between 2024-2028
Disease response and survival outcomes
d: Overall Survival (OS) • Time from initiation of treatment to death from any cause.
Time frame: Time Period between 2024-2028
Healthcare resource utilisation
a: Hospitalisation Rate • Proportion of participants requiring hospital admission during step-up dosing and the early treatment period.
Time frame: Time Period between 2024-2028
Healthcare resource utilisation
b: Length of Hospital Stay • Total number of inpatient bed-days per participant during the study period.
Time frame: Time Period between 2024-2028
Healthcare resource utilisation
c: Emergency Admission Rate • Number or proportion of participants requiring emergency admission related to CRS, ICANS, or infection.
Time frame: Time Period between 2024-2028
Healthcare resource utilisation
d: Treatment Setting • Proportion of treatment episodes delivered in the inpatient versus ambulatory/outpatient setting
Time frame: Time Period between 2024-2028
Treatment exposure, dosing and delivery intensity
a: Delivered Dose Intensity • Proportion of planned treatment delivered over the treatment period.
Time frame: Time Period between 2024-2028
Treatment exposure, dosing and delivery intensity
b: Treatment Duration • Time from first to last treatment administration.
Time frame: Time Period between 2024-2028
Treatment exposure, dosing and delivery intensity
c: Dose Delays • Number and duration of treatment delays.
Time frame: Time Period between 2024-2028
Treatment exposure, dosing and delivery intensity
d: Dose Modifications • Frequency of dose reductions, omissions, interruptions, or schedule modifications.
Time frame: Time Period between 2024-2028
Treatment exposure, dosing and delivery intensity
e: Treatment Discontinuation • Proportion of participants permanently discontinuing treatment and reason for discontinuation.
Time frame: Time Period between 2024-2028
No study locations are listed for this record.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.
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The Royal Wolverhampton Hospitals NHS Trust