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NCT04150289 Clinical Trial

A Disease Registry Encompassing the Care Of Patients With Multiple Myeloma on Panobinostat

Multiple Myeloma Clinical Trial

— RECOMM  

Official title:
A Disease Registry Encompassing the Care of Patients With Multiple Myeloma on Panobinostat (RECOMM)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04150289
Other study ID # 20192475
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 4, 2019
Est. completion date March 30, 2022

Study information
Verified date June 2023
Source zr Pharma & GmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study aims to describe current treatment patterns in the real-world setting among patients with multiple myeloma who are initiating treatment with (or changing treatment to) panobinostat and explore the associations with baseline patient characteristics, healthcare resource utilization, and clinical outcomes.

Recruitment information / eligibility
Status Completed
Enrollment 248
Est. completion date March 30, 2022
Est. primary completion date March 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Willing and able to provide written informed consent - At least 18 years of age - Clinical diagnosis of multiple myeloma that meets published diagnostic criteria - Initiating panobinostat within 60 days of enrollment - ECOG performance status 0-1 - Availability of documentation from the patient's medical records regarding previous myeloma treatment, response, and duration of response - Willing and able to complete the PRO questionnaire Exclusion Criteria: - Diagnosed with any B-cell malignancy other than myeloma - Estimated life expectancy <6 months - Currently enrolled in any interventional clinical trial at study entry (note: patients who enroll in an interventional clinical trial after enrollment may remain in the registry)

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Farydak
non-interventional study

Locations
Country Name City State
United States Oncology Specialists of Charlotte Charlotte North Carolina
United States Gettysburg Cancer Center Gettysburg Pennsylvania
United States Southern Oncology Specialists Huntersville North Carolina
United States American Health Network Indiana Indianapolis Indiana
United States Southern Nevada Cancer Research Foundation and Optum Cancer Care Las Vegas Nevada
United States Coastal Cancer Center Myrtle Beach South Carolina
United States Carolina Blood and Cancer Care Associates Rock Hill South Carolina

Sponsors (1)
Lead Sponsor Collaborator
zr Pharma & GmbH

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Response to treatment Looking for patient reproted response to treatment with panobinostat 24 months
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