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Not Yet Recruiting NCT07191379

Self-administered Subcutaneous Daratumumab in Patients With Multiple Myeloma

Conditions: Multiple Myeloma in Relapse

Sex: All
Healthy volunteers: No
Phase: PHASE4
Enrollment: 50
Sponsor: Odense University Hospital

Summary

The main goal in this open label, phase four, prospective, non-randomized, sponsor-initiated multicenter feasibility study is to evaluate the feasibility and safety of self-administration of subcutaneously (SC) daratumumab in the patients with multiple myeloma in their own home. The study intervention is self-administration of SC daratumumab by the patient, thereby changing the administration from an outpatient setting to a home setting. To reduce potential bias, patients will function as their own controls by receiving alternating treatments at home and in the outpatient clinic. To participate, patients must be scheduled for SC daratumumab alone or in combination with other drugs not necessitating outpatient visits on days of planned SC daratumumab self-administration. Patients can be included and trained during cycle 1 and 2, but only treatments administered in cycle 3-6 are considered protocol treatments. Here, patients will receive SC daratumumab once every second week with treatments at day 1 administered in the outpatient clinic and treatments at day 15 administered at home. From cycle 7 onwards, patients continues SC daratumumab outside protocol according to local standards. At inclusion, baseline demographic and clinical data should be registered for included patients. For each SC daratumumab administration in the protocol, planned treatment location (home/hospital) should be registered together with information on whether the dose was administered as planned. For each protocol treatment, regardless of treatment location, patients, caregivers, and healthcare professionals should register their time spent. In addition, patients should complete the Health Literacy Questionnaire (HLQ) and caregivers are to complete the Caregiver Roles and Responsibilities Scale (CRRS). Throughout the study, patient will also register all unplanned contacts to the healthcare system. Patient will also be asked to complete an evaluation form. Lastly, qualitative evaluations of the experience of self-administration will be conducted through semi-structured interviews with patients and caregivers, as well as focus group interviews with involved healthcare professionals.

Eligibility Criteria

Inclusion Criteria: * Diagnosed with MM * Initiating treatment with SC daratumumab * Able to read and understand the Danish language * Are considered suitable for self-administration of SC daratumumab at home (in the opinion of the healthcare professional) * Willing and able to complete questionnaires and participate in an interview Exclusion Criteria: * Resident on an unbridged island * Receiving co-treatment with other anti-myeloma treatments necessitating hospitals visits on days of home administration * Anything related to their ability to self-administer SC daratumumab at home e.g. physical inabilities or cognitive impairment

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07191379). StuddyBuddy aggregates publicly available trial information.