Open-label Study Comparing Iberdomide, Daratumumab and Dexamethasone (IberDd) Versus Daratumumab, Bortezomib, and Dexamethasone (DVd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)

NCT ID: NCT04975997

Last Updated: 2025-07-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

PHASE3

Total Enrollment

864 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-06-23

Study Completion Date

2032-06-25

Brief Summary

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This is a multicenter, two-stage, randomized, controlled, open-label, Phase 3 study comparing the efficacy and safety of iberdomide in combination with dexamethasone and daratumumab (IberDd) versus daratumumab, bortezomib, and dexamethasone (DVd) in participants with relapsed or refractory multiple myeloma (RRMM).

Detailed Description

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This is a multicenter, two-stage, randomized, controlled, open-label, Phase 3 study comparing the efficacy and safety of iberdomide in combination with dexamethasone and daratumumab (IberDd) versus daratumumab, bortezomib, and dexamethasone (DVd) in participants with relapsed or refractory multiple myeloma (RRMM). Approximately 200 patients randomized in stage 1 to one of three iberdomide dose levels of 1, 1.3, or 1.6 mg in combination with daratumumab and dexamethasone (Treatment Arms A1, A2, or A3), or to the DVd comparator arm (Treatment Arm B).

In Stage 2 of the study, approximately 664 additional subjects will be randomized 1:1 between 2 treatment arms:

* Approximately 332 subjects will be randomized to receive Treatment Arm A (IberDd)
* Approximately 332 subjects will be randomized to receive Treatment Arm B (DVd)

Participants in both treatment arms will continue to receive treatment until confirmed progressive disease (PD), unacceptable toxicity or withdrawal of consent. To ensure accuracy and completeness of the primary endpoint assessment of progression-free survival (PFS), participants who permanently discontinue study treatment for any reason, other than confirmed PD or withdrawal of consent, will continue to be followed for disease assessment.

The study will be conducted in compliance with International Council for Harmonisation (ICH) and Good Clinical Practices (GCPs).

Conditions

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Multiple Myeloma

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Daratumumab in combination with Iberdomide and dexamethasone - Dose 1

Participants will receive oral iberdomide, subcutaneous daratumumab and oral dexamethasone.

Group Type EXPERIMENTAL

Dexamethasone

Intervention Type DRUG

Oral dexamethasone 40mg on days 1, 8, 15, 22 of a 28-day cycle

Daratumumab

Intervention Type DRUG

Subcutaneous Daratumumab 1800mg on Days 1, 8, 15 and 22 for Cycles 1 to 2, on Days 1 and 15 for Cycles 3 to 6, and then on Day 1 for Cycle 7+ of a 28-day cycle

Iberdomide

Intervention Type DRUG

Oral Iberdomide 1.0mg on Days 1 to 21 of a 28-day cycle

Daratumumab in combination with Iberdomide and dexamethasone - Dose 2

Group Type EXPERIMENTAL

Dexamethasone

Intervention Type DRUG

Oral dexamethasone 40mg on days 1, 8, 15, 22 of a 28-day cycle

Daratumumab

Intervention Type DRUG

Subcutaneous Daratumumab 1800mg on Days 1, 8, 15 and 22 for Cycles 1 to 2, on Days 1 and 15 for Cycles 3 to 6, and then on Day 1 for Cycle 7+ of a 28-day cycle

Iberdomide

Intervention Type DRUG

Oral Iberdomide 1.3mg on Days 1 to 21 of a 28-day cycle

Daratumumab in combination with Iberdomide and dexamethasone - Dose 3

Group Type EXPERIMENTAL

Dexamethasone

Intervention Type DRUG

Oral dexamethasone 40mg on days 1, 8, 15, 22 of a 28-day cycle

Daratumumab

Intervention Type DRUG

Subcutaneous Daratumumab 1800mg on Days 1, 8, 15 and 22 for Cycles 1 to 2, on Days 1 and 15 for Cycles 3 to 6, and then on Day 1 for Cycle 7+ of a 28-day cycle

Iberdomide

Intervention Type DRUG

Oral Iberdomide 1.6mg on Days 1 to 21 of a 28-day cycle

Daratumumab in combination with dexamethasone and bortezomib

Participants will receive subcutaneous daratumumab, bortezomib and oral dexamethasone

Group Type ACTIVE_COMPARATOR

Dexamethasone

Intervention Type DRUG

Oral dexamethasone 40mg on days 1, 8, 15, 22 of a 28-day cycle

Bortezomib

Intervention Type DRUG

Subcutaneous Bortezomib 1.3 mg/m2 on Days 1, 4, 8 and 11 of each 21-day cycle for a total of 8 cycles.

Dexamethasone

Intervention Type DRUG

Oral dexamethasone 20mg on days 1,2, 4,5,8,9,11,12 of a 21-day cycle from cycles 1-8

Daratumumab

Intervention Type DRUG

Subcutaneous daratumumab 1800mg Cycles 1 to 3 on Days 1, 8, 15 of a 21-day cycle, Cycles 4 to 8 on Day 1 of a 21-day cycle and Cycles 9+ on Day 1 of a 28-day cycle.

Interventions

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Dexamethasone

Oral dexamethasone 40mg on days 1, 8, 15, 22 of a 28-day cycle

Intervention Type DRUG

Daratumumab

Subcutaneous Daratumumab 1800mg on Days 1, 8, 15 and 22 for Cycles 1 to 2, on Days 1 and 15 for Cycles 3 to 6, and then on Day 1 for Cycle 7+ of a 28-day cycle

Intervention Type DRUG

Bortezomib

Subcutaneous Bortezomib 1.3 mg/m2 on Days 1, 4, 8 and 11 of each 21-day cycle for a total of 8 cycles.

Intervention Type DRUG

Iberdomide

Oral Iberdomide 1.0mg on Days 1 to 21 of a 28-day cycle

Intervention Type DRUG

Iberdomide

Oral Iberdomide 1.3mg on Days 1 to 21 of a 28-day cycle

Intervention Type DRUG

Iberdomide

Oral Iberdomide 1.6mg on Days 1 to 21 of a 28-day cycle

Intervention Type DRUG

Dexamethasone

Oral dexamethasone 20mg on days 1,2, 4,5,8,9,11,12 of a 21-day cycle from cycles 1-8

Intervention Type DRUG

Daratumumab

Subcutaneous daratumumab 1800mg Cycles 1 to 3 on Days 1, 8, 15 of a 21-day cycle, Cycles 4 to 8 on Day 1 of a 21-day cycle and Cycles 9+ on Day 1 of a 28-day cycle.

Intervention Type DRUG

Other Intervention Names

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DARZALEX FASPRO CC-220 BMS-986382 CC-220 BMS-986382 CC-220 BMS-986382 DARZALEX FASPRO

Eligibility Criteria

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Inclusion Criteria

* Documented diagnosis of multiple myeloma (MM) and measurable disease.
* Received 1 to 2 prior lines of anti-myeloma therapy.
* Must have documented disease progression during or after their last anti-myeloma regimen.
* Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1 or 2.

Exclusion Criteria

* Any condition that confounds the ability to interpret data from the study.
* Has plasma cell leukemia, Waldenstrom's macroglobulinemia or POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes), or clinically significant amyloidosis.
* Known central nervous system involvement with MM.
* Prior therapy with iberdomide.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Celgene

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Bristol-Myers Squibb

Locations

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Local Institution - 035

Hot Springs, Arkansas, United States

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Local Institution - 641

Cerritos, California, United States

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Local Institution - 681

Fountain Valley, California, United States

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Local Institution - 047

Los Angeles, California, United States

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Newport, California, United States

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New Haven, Connecticut, United States

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Fort Myers, Florida, United States

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Ocala, Florida, United States

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St. Petersburg, Florida, United States

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Tamarac, Florida, United States

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West Palm Beach, Florida, United States

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Weston, Florida, United States

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Atlanta, Georgia, United States

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Local Institution - 640

Elk Grove Village, Illinois, United States

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Local Institution - 697

Dyer, Indiana, United States

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Louisville, Kentucky, United States

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Alexandria, Louisiana, United States

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Local Institution - 682

Baton Rouge, Louisiana, United States

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Baton Rouge, Louisiana, United States

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Baltimore, Maryland, United States

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Bethesda, Maryland, United States

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Columbia, Maryland, United States

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Boston, Massachusetts, United States

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Worcester, Massachusetts, United States

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Burnsville, Minnesota, United States

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Kansas City, Missouri, United States

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Billings, Montana, United States

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Summit, New Jersey, United States

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Local Institution - 691

New York, New York, United States

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Durham, North Carolina, United States

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Cincinnati, Ohio, United States

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Cleveland, Ohio, United States

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Cleveland, Ohio, United States

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Columbus, Ohio, United States

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Local Institution - 680

Tulsa, Oklahoma, United States

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Local Institution - 043

Portland, Oregon, United States

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Chattanooga, Tennessee, United States

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Nashville, Tennessee, United States

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Local Institution - 687

Austin, Texas, United States

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Houston, Texas, United States

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Newport News, Virginia, United States

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Roanoke, Virginia, United States

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Madison, Wisconsin, United States

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Ciudad Autanoma de Buenos Aires, Buenos Aires, Argentina

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Villa Elisa, Buenos Aires, Argentina

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Local Institution - 813

Birtinya, Queensland, Australia

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Douglas, Queensland, Australia

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Adelaide, South Australia, Australia

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Bedford Park, South Australia, Australia

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Clayton, Victoria, Australia

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East Melbourne, Victoria, Australia

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Melbourne, Victoria, Australia

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Murdoch, Western Australia, Australia

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West Perth, Western Australia, Australia

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Camperdown, , Australia

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Fitzroy, , Australia

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Garran, , Australia

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Graz, , Austria

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Linz, , Austria

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Salzburg, , Austria

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Sankt Pölten, , Austria

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Vienna, , Austria

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Vienna, , Austria

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Bruges, , Belgium

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Brussels, , Belgium

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Curitiba, Paraná, Brazil

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Porto Alegre, Rio Grande do Sul, Brazil

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Porto Alegre, Rio Grande do Sul, Brazil

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Barretos, São Paulo, Brazil

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Jaú, São Paulo, Brazil

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São Paulo, São Paulo, Brazil

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Rio de Janeiro, , Brazil

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São Paulo, , Brazil

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São Paulo, , Brazil

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Calgary, Alberta, Canada

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Edmonton, Alberta, Canada

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Surrey, British Columbia, Canada

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Saint John, New Brunswick, Canada

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St. John's, Newfoundland and Labrador, Canada

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Halifax, Nova Scotia, Canada

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Ottawa, Quebec, Canada

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Québec, Quebec, Canada

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Saskatoon, Saskatchewan, Canada

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Changsha, Hunan, China

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Nanchang, Jiangxi, China

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Xi'an, Shaanxi, China

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Shanghai, Shanghai Municipality, China

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Taiyuan, Shanxi, China

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Wenzhou, Zhejiang, China

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Beijing, , China

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Beijing, , China

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Beijing, , China

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Changchun, , China

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Chaoyang District, , China

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Guangzhou, , China

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Guangzhou, , China

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Hangzhou, , China

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Hangzhou, Zhejiang, , China

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Harbin, , China

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Nanjing, , China

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Shanghai, , China

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Shanghai, , China

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Shenyang, , China

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Suzhu, , China

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Tianjin, , China

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Wuhan, , China

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Xi'an, , China

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Zhengzhou, , China

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Brno, , Czechia

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Ostrava-Poruba, , Czechia

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Prague, , Czechia

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Aalborg, , Denmark

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Odense, , Denmark

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Roskilde, , Denmark

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Turku, Southwest Finland, Finland

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Helsinki, , Finland

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Oulu, , Finland

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Argenteuil, , France

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La Roche-sur-Yon, , France

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Lille, , France

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Nancy, , France

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Nantes, , France

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Paris, , France

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Paris, , France

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Pessac, , France

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Rouen, , France

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Toulouse, , France

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Kiel, Schleswig-Holstein, Germany

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Frankfurt am Main, , Germany

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Hamburg, , Germany

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Hamburg, , Germany

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Heidelberg, , Germany

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Lübeck, , Germany

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Local Institution - 573

Pátrai, Achaea, Greece

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Local Institution - 574

Pátrai, Achaia, Greece

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Local Institution - 571

Athens, , Greece

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Thessaloniki, , Greece

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Local Institution - 570

Thessaloniki, , Greece

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Local Institution - 932

Hyderabad, Andhra Pradesh, India

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Local Institution - 930

Bangalore, Karnataka, India

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Local Institution - 934

Ernākulam, Kerala, India

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Local Institution - 933

Mumbai, Maharashtra, India

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Local Institution - 935

Kolkata, West Bengal, India

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Local Institution - 931

Puducherry, , India

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Local Institution - 752

Cork, , Ireland

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Local Institution - 750

Dublin, , Ireland

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Local Institution - 751

Galway, , Ireland

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Local Institution - 874

Afula, Northern District, Israel

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Local Institution - 872

Haifa, , Israel

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Local Institution - 871

Jerusalem, , Israel

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Local Institution - 870

Tel Aviv, , Israel

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Local Institution - 873

Tel Litwinsky, , Israel

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Local Institution - 415

Rome, Lazio, Italy

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Local Institution - 400

Bologna, , Italy

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Local Institution - 408

Catania, , Italy

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Local Institution - 414

Genova, , Italy

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Milan, , Italy

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Local Institution - 410

Novara, , Italy

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Pavia, , Italy

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Pisa, , Italy

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Reggio Calabria, , Italy

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Roma, , Italy

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San Giovanni Rotondo FG, , Italy

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Udine, , Italy

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Local Institution - 900

Matsuyama, Ehime, Japan

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Higashi-Ibaraki-gun, Ibaraki, Japan

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Local Institution - 919

Shimotsuga, Tochigi, Japan

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Nerima-ku, Tokyo, Japan

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Local Institution - 918

Shinagawa-ku, Tokyo, Japan

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Local Institution - 915

Chuo-shi, Yamanashi, Japan

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Aomori, , Japan

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Chiba, , Japan

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Local Institution - 911

Fukuoka, , Japan

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Kamogawa, , Japan

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Kyoto, , Japan

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Local Institution - 910

Nagoya, , Japan

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Nagoya, , Japan

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Local Institution - 905

Okayama, , Japan

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Local Institution - 907

Osaka, , Japan

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Local Institution - 908

Ōsaka-sayama, , Japan

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Local Institution - 913

Sapporo, , Japan

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Local Institution - 914

Sendai, , Japan

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Local Institution - 906

Shibuya-ku, , Japan

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Local Institution - 909

Shinagawa-ku, Tokyo, , Japan

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Local Institution - 904

Toyohashi, , Japan

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Local Institution - 183

Guadalajara, Jalisco, Mexico

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Local Institution - 351

Dordrecht, South Holland, Netherlands

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Local Institution - 354

Amsterdam, , Netherlands

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Local Institution - 352

The Hague, , Netherlands

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Local Institution - 202

Bergen, , Norway

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Local Institution - 200

Oslo, , Norway

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Local Institution - 201

Trondheim, , Norway

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Local Institution - 631

Bialystok, Podlaskie Voivodeship, Poland

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Local Institution - 633

Krakow, , Poland

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Local Institution - 635

Nowy Sącz, , Poland

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Local Institution - 634

Poznan, , Poland

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Local Institution - 630

Warsaw, , Poland

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Local Institution - 636

Wałbrzych, , Poland

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Local Institution - 545

Coimbra, , Portugal

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Local Institution - 543

Lisbon, , Portugal

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Lisbon, , Portugal

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Local Institution - 540

Porto, , Portugal

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Porto, , Portugal

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Local Institution - 974

Daegu, , South Korea

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Local Institution - 973

Gyeonggi-do, , South Korea

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Local Institution - 975

Hwasun-gun, , South Korea

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Local Institution - 971

Seoul, , South Korea

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Local Institution - 976

Seoul, , South Korea

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Local Institution - 972

Seoul, , South Korea

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Local Institution - 970

Seoul, , South Korea

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Local Institution - 977

Seoul, , South Korea

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Local Institution - 514

Pamplona, Navarre, Spain

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Local Institution - 505

Barcelona, , Spain

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Local Institution - 502

Barcelona, , Spain

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Local Institution - 511

Barcelona, , Spain

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Local Institution - 501

Cáceres, , Spain

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Local Institution - 509

Córdoba, , Spain

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Local Institution - 510

Madrid, , Spain

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Local Institution - 516

Madrid, , Spain

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Local Institution - 504

Madrid, , Spain

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Madrid, , Spain

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Málaga, , Spain

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Murcia, , Spain

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Oviedo, , Spain

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Local Institution - 515

Salamanca, , Spain

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Santiago de Compostela, , Spain

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Local Institution - 512

Valencia, , Spain

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Local Institution - 507

Zaragoza, , Spain

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Local Institution - 272

Borås, , Sweden

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Local Institution - 271

Helsingborg, , Sweden

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Local Institution - 851

Chur, , Switzerland

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Local Institution - 850

Sankt Gallen, , Switzerland

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Local Institution - 955

Niao-Sung Hsiang Kaohsiung County, , Taiwan

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Local Institution - 952

Taichung, , Taiwan

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Local Institution - 954

Taichung, , Taiwan

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Local Institution - 951

Tainan, Taiana, , Taiwan

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Local Institution - 950

Taipei, , Taiwan

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Local Institution - 956

Taipei, Zhongzheng Dist., , Taiwan

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Local Institution - 953

Taoyuan, , Taiwan

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Local Institution - 778

Kavaklıdere, Ankara, Turkey (Türkiye)

Site Status

Local Institution - 776

Yenimahalle, Ankara, Turkey (Türkiye)

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Local Institution - 777

Pendik, Istanbul, Turkey (Türkiye)

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Local Institution - 771

Balçova, İzmir, Turkey (Türkiye)

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Local Institution - 775

Bornova, İzmir, Turkey (Türkiye)

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Local Institution - 773

Samsun, Kurupelit, Turkey (Türkiye)

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Local Institution - 770

Ankara, , Turkey (Türkiye)

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Local Institution - 772

Gaziantep, , Turkey (Türkiye)

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Local Institution - 774

Kayseri, , Turkey (Türkiye)

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Local Institution - 702

Nottingham, Nottinghamshire, United Kingdom

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Local Institution - 705

Belfast Northern Ireland, , United Kingdom

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Local Institution - 700

Birmingham, , United Kingdom

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Local Institution - 707

Canterbury Kent, , United Kingdom

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Local Institution - 704

Lancashire Blackpool, , United Kingdom

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Local Institution - 701

London, , United Kingdom

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Local Institution - 709

London, , United Kingdom

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Local Institution - 706

Oxford, , United Kingdom

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Local Institution - 711

Portsmouth, , United Kingdom

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Local Institution - 713

Sutton, , United Kingdom

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Local Institution - 708

Wolverhampton, , United Kingdom

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Countries

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United States Argentina Australia Austria Belgium Brazil Canada China Czechia Denmark Finland France Germany Greece India Ireland Israel Italy Japan Mexico Netherlands Norway Poland Portugal South Korea Spain Sweden Switzerland Taiwan Turkey (Türkiye) United Kingdom

References

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Lonial S, Dimopoulos MA, Berdeja JG, Richardson PG, Quach H, Rodriguez-Otero P, Maciag P, Hong K, Amatangelo M, Chen M, van de Donk NWCJ. EXCALIBER-RRMM: a phase III trial of iberdomide, daratumumab, and dexamethasone in relapsed/refractory multiple myeloma. Future Oncol. 2025 Jun;21(14):1761-1769. doi: 10.1080/14796694.2025.2501920. Epub 2025 May 10.

Reference Type DERIVED
PMID: 40346992 (View on PubMed)

Related Links

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Other Identifiers

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U1111-1260-2872

Identifier Type: OTHER

Identifier Source: secondary_id

2020-000431-49

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CC-220-MM-002

Identifier Type: -

Identifier Source: org_study_id

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