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NCT01632826: PEXIUS

Pomalidomide (POM) in Combination With Low Dose Dexamethasone (LD-Dex) in Patients With Relapsed or Refractory Multiple Myeloma

APPROVED FOR MARKETING Last updated 12 November 2019
What this trial tests

trial testing Pomalidomide in Multiple Myeloma. Approved for marketing.

Quick facts

Lead sponsorCelgene
StatusAPPROVED FOR MARKETING
Study typeEXPANDED_ACCESS
Sites42 locations across Canada, United States

Drugs / interventions tested

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

To provide pomalidomide access to relapsed/refractory multiple myeloma subjects with a likelihood of benefit from the pomalidomide treatment while the medication is not commercially available

Publications & conference data

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

  1. Pomalidomide: the new immunomodulatory agent for the treatment of multiple myeloma.
    Chanan-Khan AA, Swaika A, Paulus A, Kumar SK, et al · · 2013 · cited 94× · PMID 24013664 · DOI 10.1038/bcj.2013.38

Verify or expand the search:

Other trials of Pomalidomide

Trials testing the same drug.

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/NCT01632826.

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