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NCT02026505

Evaluation of Cardiotoxic Effects of Bortezomib

Completed Last updated 13 March 2019
What this trial tests

trial testing Bortezomib in Multiple Myeloma in 11 participants. Completed in 1 March 2019.

Timeline
1 March 2014
Primary endpoint
31 December 2016
1 March 2019

Quick facts

Lead sponsorOregon Health and Science University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment11
Start date1 March 2014
Primary completion31 December 2016
Estimated completion1 March 2019

Drugs / interventions tested

Conditions studied

Sponsor

Oregon Health and Science University

Who can join

Adults 18 to 70, any sex, with Multiple Myeloma or Heart Failure, Systolic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to learn more about how a drug commonly used to treat multiple myeloma can affect the heart. In this study, the investigators will learn whether a drug called how a drug (called bortezomib, or Velcade) receive for multiple myeloma affects the heart. Bortezomib is part of the standard treatment and its effects on multiple myeloma is not being studied here. The investigators want to learn whether damage occurs to the heart after taking bortezomib for multiple myeloma, whether it is reversible, and we can predict damage to the heart before it occurs.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Bortezomib

Trials testing the same drug.

Other recruiting trials for Multiple Myeloma

Currently open trials in the same condition.

Other Oregon Health and Science University 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/NCT02026505.

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