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Clinical trial

A Phase 1a/1b Multicenter, Open Label, Dose-Finding Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of CWP232291 Administered Intravenously Either Alone or in Combination With Lenalidomide and Dexamethasone in Subjects With Relapsed or Refractory Myeloma (MM)

NCT02426723 is registered in ClinicalTrials.gov with JW Pharmaceutical as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 1a/1b Multicenter, Open Label, Dose-Finding Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of CWP232291 Administered Intravenously Either Alone or in Combination With Lenalidomide and Dexamethasone in Subjects With Relapsed or Refractory Myeloma (MM)
Lead sponsor
JW Pharmaceutical
Phase
Phase 1
Overall status
Completed
Start date
October 19, 2015
Completion date
October 26, 2018
Enrollment
25 (actual)
Sites
4

Conditions

As the registry lists them; a condition with its own page is linked.