Actively Recruiting
Real World Insights During Treatment for Relapsed/Refractory Multiple Myeloma with Isatuximab
Led by Pack Health · Updated on 2024-12-11
50
Participants Needed
2
Research Sites
184 weeks
Total Duration
On this page
Sponsors
P
Pack Health
Lead Sponsor
M
M.D. Anderson Cancer Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
This descriptive study aims to evaluate the experience of adults with relapsed or refractory multiple myeloma receiving standard of care isatuximab-irfc through collection of quantitative, qualitative and wearable data. Fifty adults with relapsed or refractory multiple myeloma receiving standard of care isatuximab-irfc will be enrolled across 2 sites, The University of California San Francisco and The University of Texas MD Anderson Cancer Center. Consented participants will be enrolled in a 3-month digital health coaching program through which electronic patient reported outcomes and wearable activity data will be collected. Outcomes include treatment experience, quality of life, financial toxicity, treatment adherence, symptom burden and health self-efficacy. These will be captured by patient reported outcome measures including the Patient's Qualitative Assessment of Treatment- Real World (PQAT-RW), Patient Global Impression of Change/Severity (PGIC/S), European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC-QLQ-C30), Quality of Life Questionnaire Multiple Myeloma (QLQ-MY20), and the European QoL-5 Dimensions (EQ5D), Cancer Behavior Inventory-Brief Form (CBI-B), Center for Adherence Support Evaluation (CASE) Medication Adherence Index, Comprehensive Score for Financial Toxicity (COST) Instrument. Clinical data, including treatment history, healthcare utilization, and co-morbidities, as well as demographic data will be collected via the electronic health record from each clinical site. This data will be complemented by qualitative data from a selected cohort of study participants with a focus on treatment experience ranging from infusion burden, toxicity management, to overall quality of life. Evaluation of this data in combination will be used to better understand the treatment experience of individuals on standard of care isatuximab-irfc specifically, and with relapsed or refractory multiple myeloma generally, contributing to an existing gap in the literature regarding patient reported outcomes from diverse data sources. Outcomes will be analyzed with attention to the relationship between social determinants of health, including race, ethnicity, and geographic location, and treatment experience as reflected in both the qualitative and quantitative data.
CONDITIONS
Official Title
Real World Insights During Treatment for Relapsed/Refractory Multiple Myeloma with Isatuximab
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 or older
- Diagnosed with relapsed or refractory multiple myeloma as per FDA guidelines for isatuximab-irfc (Sarclisa4)
- Receiving or planning to receive intravenous isatuximab-irfc as standard care, with possible concurrent therapies like pomalidomide
- Have access to and willing to use a smartphone or device for texts, emails, or mobile app use
- Willing to wear a Fitbit device for activity data collection
- Able to engage in physical activity with an ECOG performance status of 2 or less
You will not qualify if you...
- Terminal illness with expected survival of 6 months or less or transitioned to comfort care only
- Documented inability to provide informed consent
- Receiving isatuximab-irfc by subcutaneous injection instead of intravenous
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
The University of Texas MD Anderson Cancer Center
Houston, Texas, United States, 77074
Active, Not Recruiting
2
University of Washington
Seattle, Washington, United States, 98109
Actively Recruiting
Research Team
K
Kelly J Brassil, PhD
CONTACT
J
Jennifer Loftis, DNP
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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