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NCT04827563

Dyspnea and Cardiotoxicity in Multiple Myeloma Patients Who Receive Carfilzomib

Terminated Last updated 4 March 2026
What this trial tests

trial testing EndoPAT in Multiple Myeloma in 50 participants. Terminated before completion.

Timeline
22 March 2021
Primary endpoint
8 September 2025
8 September 2025

Quick facts

Lead sponsorUniversity of Chicago
StatusTerminated
Study typeOBSERVATIONAL
Enrollment50
Start date22 March 2021
Primary completion8 September 2025
Estimated completion8 September 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Chicago

Who can join

18 and older, any sex, with Multiple Myeloma or Shortness of Breath. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will explore why some multiple myeloma patients who receive carfilzomib (an anti-cancer medication) experience shortness of breath while others do not. The purpose of this research is to gather information on the effectiveness of the EndoPAT device, which is FDA-approved to assess the health of a patient's blood vessels. These assessments will help doctors leading the study determine the reasons why patients may develop shortness of breath (dyspnea) when being treated with carfilzomib and ways to better prevent this shortness of breath.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of EndoPAT

Trials testing the same drug.

Other recruiting trials for Multiple Myeloma

Currently open trials in the same condition.

Other University of Chicago trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04827563.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing