RecruitingNCT06846905

Cost-utility Analysis of Ambulatory Dose Escalation of Bispecific Antibodies in Multiple Myeloma.


Sponsor

University Hospital, Toulouse

Enrollment

40 participants

Start Date

Jan 20, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

Multiple myeloma is the second most common haematological cancer. Recent innovations have made it possible for relapsed/refractory patients to benefit from the innovative immunotherapy of bispecific antibodies. These antibodies stimulate the immune system to attack tumour cells. The treatment involves an escalating dose of three subcutaneous injections every 2 to 4 days for a total of about 10 days, followed by a weekly treatment phase. The University Hospital of Toulouse was the first centre in France to offer outpatient dose escalation for this innovative treatment. This form of treatment depends on clinical and logistical feasibility. Where appropriate, patients are treated in a conventional unit. An analysis carried out at Toulouse University Hospital suggests a response to treatment, with no increased risk of complications in the outpatient setting. Patients' quality of life may also be unaffected. In addition, given the increasing demand for care in a context of finite resources, the economic evaluation of healthcare initiatives is becoming essential if we are to maintain a high-quality healthcare system that is accessible to all.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is looking at the costs and benefits of giving patients their bispecific antibody cancer treatment (a type of targeted immunotherapy) in an outpatient clinic — rather than staying in hospital — when their dose is being increased at the start of treatment for multiple myeloma (a blood cancer). **You may be eligible if...** - You have multiple myeloma that has come back or stopped responding to previous treatment - You are being treated with teclistamab, elranatamab, or talquetamab - You are over 18 years old - You live within 30 minutes of the IUCT Oncopole and can stay nearby for 48 hours after each dose increase, OR you are receiving inpatient care at the IUCT Oncopole - You are in reasonably good health (no serious active infection or rapidly progressing disease) **You may NOT be eligible if...** - You are unable to read or have a significant language barrier Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

CHU de Toulouse

Toulouse, France

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NCT06846905


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