Plain-English translation of NCT03616483 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
The Indiana Myeloma Registry is a research database that collects blood samples and medical information from patients diagnosed with or suspected of having plasma cell disorders—conditions including MGUS, smoldering myeloma, multiple myeloma, plasmacytoma, and primary amyloidosis. The study does not test a specific medication or treatment; instead, it builds a resource that researchers can use to better understand these blood cancers and develop new therapies in the future.
Researchers need access to real patient samples and medical histories to understand how plasma cell disorders develop and progress, and to test new treatments. By creating this registry, scientists can study these diseases more effectively and work toward better care options for patients.
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Participation involves donating blood or tissue samples and allowing researchers access to your medical records related to your diagnosis. You will share clinical information about your disease and treatment history with the study team. The study is observational, meaning you will not receive a new treatment—researchers will simply collect and store your samples and data to support future research efforts.
AI-generated summary from trial data · Aug 2, 2026 · Not medical advice
United States
Enrollment target
~2,500 participants
Started
June 2018
Primary completion
June 2028
Age range
18 Years and older
Last updated on clinicaltrials.gov in November 2025.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Attaya Suvannasankha, MD
Indiana University
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.