The Indiana Myeloma Registry

Indiana University2,500 enrolled

Overview

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

Study Type

OBSERVATIONAL

Enrollment

2,500

Conditions

Plasma Cell Dyscrasias

Interventions

This is a non-interventional trialOTHER

This is a non-interventional trial

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Indiana University Simon Cancer Center

Indianapolis, Indiana, United States

RECRUITING

Outcomes

Primary Outcomes

Create a repository

The 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

Time frame: 5 years

Secondary Outcomes

Data collection

To 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.

Time frame: 5 years

Central Contacts

Attaya Suvannasankha, MD

CONTACT

317-274-0843 asuvanna@iu.edu

Nisha George, MD

CONTACT

(317) 274-6635 nishgeor@iu.edu

Data from ClinicalTrials.gov

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