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A Study to Determine Dose, Safety, Tolerability and Efficacy of CC-220 Monotherapy, and in Combination With Other Treatments in Subjects With Multiple Myeloma

Active, not recruiting · Phase 1, Phase 2 · NCT02773030

Conditions: Multiple Myeloma

At a glance

Research payments reported, 2025
$1.5M
U.S. investigators named
18
Sites paid
18
Planned or actual enrollment
466

About the trial

Sponsor
Celgene
Tested
CC-220 (drug), Dexamethasone (drug), Daratumumab (drug), Bortezomib (drug), Carfilzomib (drug), Daratumumab - 16mg/kg (drug), Bortezomib (BTZ) (drug), Daratumumab- 1800mg (drug)
Dates
Started 2016-10-14; completion 2028-07-28
Results posted
Yes

This is a multicenter, multi-country, open-label, Phase 1b/2a dose-escalation study consisting of two parts: dose escalation (Part 1) for CC-220 monotherapy, CC-220 in combination with DEX, CC-220 in combination with DEX and DARA, CC-220 in combination with DEX and BTZ and CC-220 in combination with DEX and CFZ; and the expansion of the RP2D (Part 2) for CC-220 in combination with DEX for Relapsed Refractory Multiple Myeloma and CC-220 in combination with DEX and BTZ for Newly Diagnosed Multiple Myeloma.

From ClinicalTrials.gov, last updated 2026-03-20. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Celgene Corporation reported $1.5M in research payments for this study in 2025 (20 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.