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Clinical Trials/NCT04150289
NCT04150289
Completed
Not Applicable

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

pharmaand GmbH7 sites in 1 country248 target enrollmentStarted: November 4, 2019Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
248
Locations
7
Primary Endpoint
Response to treatment

Overview

Brief 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.

Study Design

Study Type
Observational
Observational Model
Ecologic Or Community
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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)

Outcomes

Primary Outcomes

Response to treatment

Time Frame: 24 months

Looking for patient reproted response to treatment with panobinostat

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (7)

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