CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 466 enrolled
Drug / intervention
CC-220 +7 moredrug
Likely dose
Daratumumab - 16mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02773030
NCT02773030Phase 2Active

Phase 1b/2a Multicenter, Open-label, Dose-escalation Study to Determine the Maximum Tolerated Dose, Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of CC-220 As Monotherapy and in Combination With Other Treatments in Subjects With Multiple Myeloma

Celgene·interventional·Posted May 16, 2016·Updated Mar 20, 2026

In Brief

A Phase 2 clinical trial evaluating CC-220, Dexamethasone, and 6 other interventions for Multiple Myeloma. Active but no longer recruiting, targeting 466 participants across 162 sites in 11 countries.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Canada, France, Germany, Israel, Italy, Japan, Netherlands, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 2Active
201720182019202020212022202320242025202620272028
First PostedMay 16, 2016
Enrollment StartOct 14, 2016
Primary CompletionMay 9, 2024
Study CompletionJul 28, 2028
TodayJul 2, 2026
Enrollment to primary: 7.6 yearsPosted 10.1 years ago

Interventions

CC-220drug

CC-220 at dose specified by cohort dose level from Day 1-21 of each 28-day cycle.

Dexamethasonedrug

Oral DEX 40 mg on Days 1, 8, 15, and 22 of each 28-day cycle. For subjects \>75 years old, oral DEX will be administered at 20 mg on Days 1, 8, 15, and 22 of each 28-day cycle.

Daratumumabdrug

Specified dose on specified days

Bortezomibdrug

Specified dose on specified days

Carfilzomibdrug

Intravenous (IV) CFZ administered at a starting dose of 20 mg/m2 on C1D1 and C1D2; and at a dose level specified by cohort dose level thereafter Days 1, 2, 8, 9, 15, 16 of each 28-day cycle.

Daratumumab - 16mg/kgdrug

Daratumumab (DARA) 16mg/kg by intravenous infusion on Days 1, 8, 15, and 22 at cycle 1-2, Days 1, 15 at cycle 3-6, and Day 1 at cycle ≥7 of each 28-day cycle.

Bortezomib (BTZ)drug

Bortezomib 1.3 mg/m\^2 on Days 1, 4, 8 and 11 at cycle 1-8, and Days 1, 8 at cycle ≥9 of each 21-day cycle.

Daratumumab- 1800mgdrug

Daratumumab (DARA) 1800 mg by subcutaneous injection on Days 1, 8, 15, and 22 at cycle 1-2, Days 1, 15 at cycle 3-6, and Day 1 at cycle ≥7 of each 28-day cycle.