Last reviewed · How we verify

NCT02946333: QoLMMBuS

A Study to Assess Disease Burden, in Terms of Health-related Quality of Life and Direct Healthcare Costs, in Patients With Newly Diagnosed Multiple Myeloma Who Are Not Candidates for Autologous Stem Cell Transplant (ASCT) in Spain

Completed Last updated 22 November 2022
What this trial tests

trial in Multiple Myeloma in 355 participants. Completed in 31 October 2022.

Timeline
25 December 2016
Primary endpoint
31 October 2022
31 October 2022

Quick facts

Lead sponsorCelgene
StatusCompleted
Study typeOBSERVATIONAL
Enrollment355
Start date25 December 2016
Primary completion31 October 2022
Estimated completion31 October 2022
Sites65 locations across Spain

Conditions studied

Sponsor

Celgene — full company profile →

Who can join

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

Sponsor's own description

Those patients with newly diagnosed Multiple Myeloma (MM) who are not candidates for Autologous Stem Cell Transplant (ASCT) and who meet the screening criteria described in this protocol can participate. The participating patients must sign an informed consent, which the investigator who will collect the study variables in an electronic case report form (eCRF) will provide to them. The investigators must recruit at least 450 patients in a 24-month period.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Abstract Book: 25th Congress of the European Hematology Association Virtual Edition, 2020
    · 2020

Verify or expand the search:

Other recruiting trials for Multiple Myeloma

Currently open trials in the same condition.

Other Celgene 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/NCT02946333.

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