RecruitingPhase 3NCT07649525

Personalising Treatment for Myeloma Patients Based on Initial Response to NHS Treatment and Their Overall Fitness Level

iFIT (UK-MRA Myeloma XVIII): Immunotherapy Approaches Adapted for Fitness in Newly Diagnosed Transplant Ineligible Patients With Myeloma


Sponsor

University of Leeds

Enrollment

1,226 participants

Start Date

Jul 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

iFIT is a trial for newly diagnosed transplant-ineligible patients with the bone marrow cancer myeloma. These patients are generally older and have a lower level of fitness than others. Patients can take part if their doctor would otherwise recommend the standard NHS treatment daratumumab, lenalidomide and dexamethasone (DRd). After six months of DRd, the subsequent treatment a patient receives in iFIT is based on two factors: the patient's fitness level and treatment response. The trial compares different treatment strategies to determine whether outcomes can be improved for specific patient groups.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Daratumumab, a drug called Dexamethasone, and others for people with multiple myeloma (mm) and plasma cell leukemia (pcl). The study is currently recruiting participants at 5 locations. People eligible for this study include aged 18 Years and older.

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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGDaratumumab

Participants will receive daratumumab by subcutaneous injection. Each cycle is 28 days.

DRUGLenalidomide

Taken orally as capsules. Each cycle is 28 days. Dose can be adjusted for frailty and renal function.

DRUGDexamethasone

Taken as oral tablets, oral solution, or given by IV. Each cycle is 28 days. Dose can be adjusted for frailty and renal function.

DRUGTeclistamab

Participants will receive teclistamab by subcutaneous injection. Each cycle is 28 days.

DRUGTalquetamab

Participants will receive talquetamab by subcutaneous injection. Each cycle is 28 days.


Locations(5)

Bristol Haematology and Oncology Centre

Bristol, United Kingdom

Eastbourne District General Hospital

Eastbourne, United Kingdom

St James University Hospital

Leeds, United Kingdom

The Clatterbridge Cancer Centre - Liverpool

Liverpool, United Kingdom

The Royal Marsden Hospital

London, United Kingdom

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07649525


Related Trials