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The Indiana Myeloma Registry

Collection of Specimens and Clinical Data to Create A Bio-repository for the Multiple Myeloma Program: The Indiana Myeloma Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03616483
Enrollment
2500
Registered
2018-08-06
Start date
2018-06-18
Completion date
2028-06-30
Last updated
2025-11-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Plasma Cell Dyscrasias

Keywords

Multiple myeloma, Monoclonal gammopathy of undetermined significance, Plasmacytoma, Smoldering multiple myeloma

Brief summary

This is a prospective, non-interventional, observational study. The purpose of this study is to collect data and bio-specimens that will support future research

Interventions

OTHERThis is a non-interventional trial

This is a non-interventional trial

Sponsors

Indiana University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or female patients ≥ 18 years of age at the time of informed consent 2. Has been diagnosed with or is suspected to have one of the following: 1. Monoclonal Gammopathy of Undetermined Significance (MGUS) 2. Smoldering Multiple Myeloma 3. Multiple Myeloma 4. Bony or Soft Tissue Plasmacytoma 5. Primary Amyloidosis

Exclusion criteria

\< 18 years of age Have not been diagnosed with one of the following: Monoclonal Gammopathy of Undetermined Significance (MGUS) b.Smoldering Multiple Myeloma c.Multiple Myeloma d.Bony or Soft Tissue Plasmacytoma e.Primary Amyloidosis

Design outcomes

Primary

MeasureTime frameDescription
Create a repository5 yearsThe primary objective of this study is to provide a mechanism to store comprehensive clinical, genomic, demographic, social, environmental and quality of life data from subjects with plasma cell dyscrasias

Secondary

MeasureTime frameDescription
Data collection5 yearsTo collect data related to clonal evolution, tumor microenvironment, clinical outcomes, adverse events, environmental factors and quality of life that will provide the foundation to create hypotheses for future confirmatory studies.

Countries

United States

Contacts

Primary ContactAttaya Suvannasankha, MD
asuvanna@iu.edu317-274-0843
Backup ContactNisha George, MD
nishgeor@iu.edu(317) 274-6635

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026