Study comparing iberdomide, daratumumab and dexamethasone versus daratumumab, bortezomib and dexamethasone in patients with relapsed or refractory multiple myeloma

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What is this study about?

This study focuses on patients with Multiple Myeloma, a type of blood cancer that has either not responded to previous treatment or has returned after treatment (known as relapsed or refractory). The study compares two different combination treatments. The first combination includes Iberdomide (also known as CC-220), Daratumumab, and Dexamethasone. The second combination consists of Daratumumab, Bortezomib, and Dexamethasone.

The purpose of this study is to determine which treatment combination works better in treating patients with relapsed or refractory Multiple Myeloma. The medications are given in different ways – some are taken by mouth as tablets or capsules, while others are given through injection under the skin or into a vein. The treatment will continue as long as it remains beneficial for the patient and side effects are manageable.

During the study, doctors will monitor how well the treatments work by checking the amount of cancer cells in the blood and bone marrow. They will also track how long patients live without their disease getting worse and evaluate the overall survival of patients receiving these treatments. Throughout the study, patients will have regular check-ups to monitor their health and any side effects from the treatments.

1 Initial assessment

Your eligibility for the study will be confirmed based on your multiple myeloma diagnosis and previous treatments

You must have received 1-2 prior treatments for multiple myeloma

You must have shown improvement with at least one previous treatment

Your current physical condition will be evaluated using the ECOG performance status scale

2 Treatment assignment

You will be randomly assigned to one of two treatment groups:

Group 1: IberDd – Iberdomide (capsules taken by mouth) + Daratumumab (injection under the skin) + Dexamethasone (tablets taken by mouth)

Group 2: DVd – Daratumumab (injection under the skin) + Bortezomib (tablets taken by mouth) + Dexamethasone (tablets taken by mouth)

3 Treatment period

Regular assessments will monitor your response to treatment

Blood samples will be taken to measure the level of disease markers

Bone marrow samples will be collected to check for remaining cancer cells

Your overall health and any side effects will be monitored throughout the treatment

4 Follow-up period

Your health will continue to be monitored after completing treatment

Regular checks will track if the disease returns or progresses

Quality of life assessments will be conducted using questionnaires

The study will continue until September 2028

5 Safety requirements

You must follow specific pregnancy prevention measures throughout the study

Blood donation is not permitted during treatment and for 28 days after

Regular pregnancy testing is required for individuals who can become pregnant

Additional safety measures will be explained based on your assigned treatment group

Who Can Join the Study?

  • Must be at least 18 years old
  • Must have been diagnosed with Multiple Myeloma with measurable disease levels
  • Must have received one to two previous treatments for multiple myeloma
  • Must have shown positive response (improvement) to at least one previous treatment
  • Must have evidence that the disease has progressed during or after the last treatment
  • Must have a performance status score of 0, 1, or 2 (measure of patient’s ability to perform daily activities)
  • Must be willing and able to follow the study schedule and requirements
  • Must sign an informed consent form before any study procedures
  • For those who can become pregnant:
    • Must have two negative pregnancy tests
    • Must agree to ongoing pregnancy testing
    • Must use two forms of birth control or practice abstinence
  • For male participants:
    • Must use contraception or practice abstinence during the study and for specified time after
    • Must not donate sperm during the study and for specified time after
  • Must not donate blood during the study and for 28 days after treatment ends
  • Must follow all requirements of the Pregnancy Prevention Program
  • If previously treated with certain medications (CD38-directed therapy):
    • Must have shown positive response to that treatment
    • Must not have had disease progression within 60 days of last dose
    • Must have stopped treatment at least 3 months before joining study

Who Cannot Join the Study?

  • Prior treatment with iberdomide (an experimental drug for multiple myeloma)
  • Active central nervous system involvement of multiple myeloma
  • Known allergy or sensitivity to any of the study medications
  • Previous stem cell transplant within 12 weeks before starting the study
  • Significant heart conditions including heart failure or recent heart attack (within 6 months)
  • Active or chronic liver disease
  • Other types of cancer requiring treatment (except for successfully treated skin cancer or cervical cancer)
  • Uncontrolled high blood pressure
  • Serious infections requiring treatment
  • Pregnancy or breastfeeding
  • Unable to take blood-thinning medications
  • Major surgery within 2 weeks before starting the study
  • Peripheral neuropathy (nerve damage causing numbness or tingling) grade 2 or higher
  • Participation in other clinical trials within 28 days before this study
  • Mental conditions that could interfere with following study procedures
  • Unable to take oral medications

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Medical University Of Vienna Vienna Austria
Hospital Universitario De Salamanca Salamanca Spain
Centre Hospitalier Universitaire De Lille Lille France
Oslo Universitetssykehus HF Oslo Norway
Hospital Universitario Y Politecnico La Fe Valencia Spain
Hospital Universitario De Navarra Pamplona Spain
Medical University Of Graz Graz Austria
Oncopole Claudius Regaud Toulouse France

Other Sites

Site Name City Country Status
University Hospital Ostrava Ostrava Czechia
Turku University Hospital Turku Finland
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
Specjalistyczny Szpital Im. Dra Alfreda Sokolowskiego Walbrzych Poland
Az St-Jan Brugge-Oostende A.V. Brugge Belgium
Uniwersytecki Szpital Kliniczny W Poznaniu Poznan Poland
Hopital Beaujon Clichy France
Cpzfay Hlnutlwpuhd Dwxkkexielavh Vzrxpq La Roche sur Yon France
Agdsbglxk Kckcumay Hkwhtpc Gldh Hamburg Germany
Hemn Hhtnnbwv Hague The Netherlands
Civnsj Hqvwyvewhij Vhiusp Dclkbl Argenteuil France
Ndz Lpl Gizjsrhaqg Rsrhri Mapij Gxmb St. Poelten Austria
Humwnges Vnvh djoezose Barcelona Spain
Bkdnojom Hukttmtb Dublin Ireland
Olmjto Uofawkoocv Hvboopcj Odense Denmark
Funxjoamob Iimeq Cj Gjchjl Oryilgcn Modzvwij Pursoxqzeup Milan Italy
Aerxgrtyy Uks Amsterdam The Netherlands
Aqklazjxs Hqgjvzia Athens Greece
Hnmrl Befdjq Hg Bergen Norway
Fqbvtgwe Nnunhkbgh Bgzh Brno Czechia
Hppuvmml Usdykjfhpz Cmldtyl Hoeuaqgd Helsinki Finland
Hplxxtxq Uujykgnvigcpg Fihefjrns Jkzhxmw Dglv Madrid Spain
Iupjf Ogzkadgf Pkylepbichx Slw Mwelmxi Genoa Italy
Uxxvgmgnls Cnbbchiz Hnixruyn Vwwvdv Dk Lo Aqrklbai Murcia Spain
Uudwozuauuad Dn Symzaxop Di Clhokqzhsu Santiago De Compostela Spain
Shkhtkjdvsi Pggqrzhby Zjphom Obsdhq Zqtresglsn Spnmrgq Upbrzjabthjlf W Kpdohbym Cracow Poland
Audzkoz Utdaonuazh Hwlbqyjc Aalborg Denmark
Ullokwhhluosyadjosevq Hjyexnhjyz Azj Heidelberg Germany
Azzfgnz Ooskgjyatiofsngcsggzpdoir Mjkoudmw Dldsy Ccphfb Novara Italy
Adcbitu Utzug Sypxzulon Lpdffw Dl Bmcgmrl Bologna Italy
Hynoennr Du Ln Szrry Clki I Sibu Pkf Barcelona Spain
Ubedfdsvkz Milkvme Ceptwd Hxehmjommwewdwwlb Hamburg Germany
Onqyendehhradx Lqiy Gqnz Linz Austria
Aqxvkdf Stdbuwapu Upjgissllqhsa Fmhugw Cwgkbnax Udine Italy
Hqhtohke Urmrbsmvwzwsn Df Lz Pmdfwcjk Madrid Spain
Gvbvwh Ntlcruwdro Tsbnjpsroyydb Gqcphq Pkixqsuhekto Thessaloniki Greece
Svhji Wcrq Waxflc Gwsafptqsucxtjsrep Vienna Austria
Olfz Uysiodgrel Hehlunyn Oulu Finland
Hkzgxedr Udfsjgurlcmqp Vqssdd De Lg Vhiodwpw Malaga Spain
Cxtvrf Hixqi Blyzuhfld Rouen France
Aeenkjs Oiqwurzijvfwtzwtwmufoxdyu Ppyjgwybwry Gu Rwwgqqwpeyic Msinp De Ctpndve Catania Italy
Gwekuy Opwirrjm Myevbsxehtwpc Bfciczj Mlmwsnkuq Mxzaxzs Reggio Calabria Italy
Tyyklpnhqq Cvrhid Hbngjaib Thessaloniki Greece
Ubnyoyxmajdpo Suinpwr Krlwonwny W Bcqtzbxwjpm Bialystok Poland
Srsivjs Svekbfpqcvhgvoe Ily Jmwkdpgx Spnwqxswgskz W Nxflo Savry Nowy Sacz Poland
Cbvnbmpkpcwq Clzeopiu Cpikuq Lisbon Portugal
Uexvgqdoen Hoivyizh Gfzqhi Galway Ireland
Gxxmoe Uxoegwxhxk Fajhrsduj Frankfurt Germany
Adflfsl Okmwkjduripbysoifmqrpfqju Szxb Aehgr Rome Italy
Cqoq Saxgrzoi Dsjuq Sbosqqpvfx San Giovanni Rotondo Italy
Cgaf Umtakmoeqt Hsyqocze Cork Ireland
Sxrwgm Aldirnpxe Hyqdcwjz Vplwbqp Gdcfozjnaamoaemxmb Boras Sweden
Slq Osdlq Higqxkvf Ho Trondheim Norway
Hjldinzj Sjm Phsog Db Awysgnnpa Caceres Spain
Razgny Svbcr Hnmbzvzkdtv Hwbegssd Helsingborg Sweden
Sbkl Ckkut Gmtdpfjbhu Salzburg Austria
Aqsnwb Szjvsirxip Zfgfppexoy Dordrecht The Netherlands
Hvmhrcgh Unsntcbvvccci Hkefbfct Tzmnb y Pcmgjt Ilacblph Cezabf dzbxdzlexqqlvmsen (whvy Badalona Spain
Ojmpemrw Thrrbeptvohps Gqezhdi Ctafxb Or Prufix Siur Patras Greece
Ccdgku Hloebujzcp E Uptimlhdfxmnv Dd Ckkpegs Eoohid Coimbra Portugal
Axnbkso Orejdmjympa Uukkttkkfeqek Ptubrj Pisa Italy
Vbsfioxmr Fuodxblj Nzodzecnh V Popyi Prague Czechia
Nocqoijf Itssikkv Omlgrpigp Ioo Murod Syybnhuksnmrsfvbliiqxzukcxrg Inyzqzbu Bnrauakg Cracow Poland
Rncwot Sdqlopmar Holbæk Denmark
Crjn Dr Nnrba Vandoeuvre Les Nancy France

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
11.06.2021
Belgium Belgium
Not recruiting
11.06.2021
Czechia Czechia
Not recruiting
11.06.2021
Denmark Denmark
Not recruiting
11.06.2021
Finland Finland
Not recruiting
11.06.2021
France France
Not recruiting
11.06.2021
Germany Germany
Not recruiting
11.06.2021
Greece Greece
Not recruiting
11.06.2021
Ireland Ireland
Not recruiting
11.06.2021
Italy Italy
Not recruiting
11.06.2021
Norway Norway
Not recruiting
11.06.2021
Poland Poland
Not recruiting
11.06.2021
Portugal Portugal
Not recruiting
11.06.2021
Spain Spain
Not recruiting
11.06.2021
Sweden Sweden
Not recruiting
11.06.2021
The Netherlands The Netherlands
Not recruiting
11.06.2021

Trial locations

Iberdomide (also known as BMS-986382) is a medication being studied for treating relapsed or refractory multiple myeloma. It belongs to a new class of drugs that helps the immune system fight cancer cells.

Daratumumab is an antibody medication that targets specific proteins on myeloma cells. It works by helping the body’s immune system recognize and destroy cancer cells in multiple myeloma.

Dexamethasone is a corticosteroid medication that helps reduce inflammation and suppress the immune system. In multiple myeloma treatment, it is often combined with other medications to enhance their effectiveness.

Bortezomib is a targeted therapy that belongs to a class of drugs called proteasome inhibitors. It works by blocking certain proteins that help cancer cells survive, causing the cancer cells to die.

Investigated Diseases:

Multiple Myeloma – A blood cancer that develops in plasma cells, which are white blood cells that help fight infections. In this condition, cancerous plasma cells accumulate in the bone marrow and crowd out healthy blood cells. These abnormal cells produce large amounts of defective antibodies that build up in the body. The disease typically affects multiple bones in the body, hence its name. Over time, the condition can damage bones, lead to high blood calcium levels, and cause problems with blood cell production. The disease often progresses through cycles of active disease and remission.

Relapsed Multiple Myeloma – A form of multiple myeloma that has returned after a period of remission or response to previous treatment. The disease shows signs of progression after a period when it was under control.

Refractory Multiple Myeloma – A form of multiple myeloma that does not respond to current therapy, or stops responding during treatment. The disease continues to progress despite ongoing treatment efforts.

Trial ID:
2024-510800-35-00
Protocol code:
CC-220-MM-002
Trial Phase:
Therapeutic confirmatory (Phase III)

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