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Clinical trial

A Phase IB Multicenter, Open-label Study To Determine The Recommended Dose And Regimen Of Durvalumab (MEDI4736) Either As Monotherapy or In Combination With Pomalidomide (POM) With Or Without Low-Dose Dexamethasone (DEX) In Subjects With Relapsed And Refractory Multiple Myeloma (RRMM)

NCT02616640 is registered in ClinicalTrials.gov with Celgene as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase IB Multicenter, Open-label Study To Determine The Recommended Dose And Regimen Of Durvalumab (MEDI4736) Either As Monotherapy or In Combination With Pomalidomide (POM) With Or Without Low-Dose Dexamethasone (DEX) In Subjects With Relapsed And Refractory Multiple Myeloma (RRMM)
Lead sponsor
Celgene
Phase
Phase 1
Overall status
Completed
Start date
January 11, 2016
Completion date
July 30, 2024
Enrollment
114 (actual)
Sites
22

Conditions

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