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Multiple MyelomaPhase 2/3NCT07095452

A Study to Assess A Change in Disease Activity and Adverse Events of Intravenous Etentamig and Daratumumab (Etentamig+D) Compared to Daratumumab, Lenalidomide, and Dexamethasone (DRd) in Adult Participants With Newly Diagnosed Multiple Myeloma Not Eligible for Transplant

A Phase 2/3 study testing Etentamig, Lenalidomide and Daratumumab in people with Multiple Myeloma, run by AbbVie at 49 sites in 4 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

Multiple myeloma (MM) is a cancer of the blood's plasma cells. The cancer is typically found in the bones and bone marrow (the spongy tissue inside of the bones) and can cause bone pain, fractures, infections, weaker bones, and kidney failure. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Multiple Myeloma
What is being tested?
Etentamig, Lenalidomide and Daratumumab
Could I receive a placebo?
No, everyone receives an active treatment
How many people
680 participants
Where
49 sitesin 4 countries
Study dates
8 Jan 2026to Jan 2042
Phase
Phase 2/3

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Participants must have confirmed new diagnosis of multiple myeloma (NDMM) according to the International Myeloma Working Group (IMWG) diagnostic criteria, and per investigator's judgement, participant is not suitable to receive high-dose chemotherapy and stem cell transplantation due to factors likely to have a negative impact on tolerability of high dose chemotherapy and autologous stem cell transplants (ASCT).
  • IMWG Myeloma Frailty Index Score of >= 1
  • All participants must have measurable disease per central laboratory with at least 1 of the following assessed within 28 days prior to enrollment:
  • Serum M-protein >= 0.5 g/dL (>= 5 g/L).
  • Urine M-protein >= 200 mg/24 hours.
  • Serum free light chain (FLC) >= 100 mg/L (>= 10 mg/dL) (involved light chain) and an abnormal serum kappa lambda ratio only for participants without measurable serum or urine M-protein.

Who cannot join

  • Prior or current systemic therapy or stem cell transplant (SCT) for multiple myeloma or any plasma cell dyscrasia other than short course of corticosteroids
  • Participant treated with any investigational treatment within 30 days or 5 half-lives of the treatment (whichever is longer) prior to the first dose of study treatment or is currently enrolled in another clinical study
  • Participant who has known active central nervous system involvement of MM.
  • Participant who has history of clinically significant renal, neurologic, psychiatric, endocrine, metabolic, immunologic, pulmonary, or hepatic disease within the last 6 months that, in the investigator's opinion, would adversely affect the participant's participation in the study.

Trial locations and contacts

49 sites in 4 countries. Contact the study team or a site near you to ask about taking part.

49 sites in 4 countries

United States17 sites, 17 recruiting
  • Winship Cancer Institute of Emory University /ID# 277667

    Atlanta, Georgia, 30322

    Recruiting
  • University of North Carolina at Chapel Hill /ID# 277708

    Chapel Hill, North Carolina, 27514

    Recruiting
  • Colorado Blood Cancer Institute /ID# 279080

    Denver, Colorado, 80218

    Recruiting
  • Willamette Valley Cancer Institute and Research Center /ID# 278721

    Eugene, Oregon, 97401

    Recruiting
  • Virginia Cancer Specialists - Fairfax /ID# 278716

    Fairfax, Virginia, 22031

    Recruiting
  • Fort Wayne Medical Oncology And Hematology /ID# 278141

    Fort Wayne, Indiana, 46804

    Recruiting
  • Cedars-Sinai Medical Center /ID# 278238

    Los Angeles, California, 90048

    Recruiting
  • Minnesota Oncology - Minneapolis Clinic /ID# 278720

    Minneapolis, Minnesota, 55404

    Recruiting
  • SCRI Oncology Partners /ID# 278353

    Nashville, Tennessee, 37203

    Recruiting
  • Icahn School of Medicine at Mount Sinai /ID# 277844

    New York, New York, 10029

    Recruiting
  • Memorial Sloan Kettering Cancer Center - New York - York Avenue /ID# 277946

    New York, New York, 10065

    Recruiting
  • Weill Cornell Medicine Myeloma Center /ID# 278216

    New York, New York, 10065

    Recruiting
  • Blue Ridge Cancer Care - Roanoke /ID# 278722

    Roanoke, Virginia, 24014

    Recruiting
  • Mayo Clinic Hospital Rochester /ID# 277886

    Rochester, Minnesota, 55905

    Recruiting
  • Mayo Clinic Hospital Scottsdale /ID# 278349

    Scottsdale, Arizona, 85259

    Recruiting
  • Texas Oncology - The Woodlands /ID# 278726

    The Woodlands, Texas, 77380

    Recruiting
  • Texas Oncology - Northeast Texas /ID# 278725

    Tyler, Texas, 75702

    Recruiting

Other trials in United States

France15 sites, 15 recruiting
  • Centre Hospitalier De Dunkerque-Hospital Alexandra Lepeve /ID# 278399

    Dunkirk, Hauts-de-France, 59385

    Recruiting
  • Centre Hospitalier Annecy Genevois /ID# 278406

    Epagny Metz Tessy, Auvergne-Rhône-Alpes, 74370

    Recruiting
  • Chu De Lille - Hopital Claude Huriez /ID# 278413

    Lille, Hauts-de-France, 59037

    Recruiting
  • CHU de Montpellier - Hopital Saint Eloi /ID# 278415

    Montpellier, Herault, 34295

    Recruiting
  • Centre Hospitalier Universitaire de Nantes, Hotel Dieu -HME /ID# 278402

    Nantes, Pays de la Loire Region, 44000

    Recruiting
  • Hopital Saint-Louis /ID# 278429

    Paris, 75010

    Recruiting
  • Hopital Saint Antoine /ID# 278428

    Paris, 75012

    Recruiting
  • Hopital Universitaire Necker Enfants Malades /ID# 278426

    Paris, Île-de-France Region, 75015

    Recruiting
  • Centre Hospitalier Universitaire de Bordeaux /ID# 278419

    Pessac, New Aquitaine, 33604

    Recruiting
  • HCL - Hopital Lyon Sud /ID# 282145

    Pierre-Bénite, Rhone, 69495

    Recruiting
  • Centre Hospitalier Universitaire de Poitiers /ID# 278398

    Poitiers, New Aquitaine, 86021

    Recruiting
  • Centre Hospitalier Universitaire de Saint Etienne - Hopital Nord /ID# 278421

    St-Priest-en-Jarez, Pays de la Loire Region, 42270

    Recruiting
  • IUCT Oncopole /ID# 278403

    Toulouse, Occitanie, 31059

    Recruiting
  • CHRU Tours - Hopital Bretonneau /ID# 279274

    Tours, Indre-et-Loire, 37044

    Recruiting
  • CH Bretagne Atlantique /ID# 278422

    Vannes, Morbihan, 56000

    Recruiting

Other trials in France

Spain12 sites, 12 recruiting
  • Institut Catala d Oncologia - ICO - Badalona /ID# 278522

    Badalona, Barcelona, 08916

    Recruiting
  • Hospital Clinic de Barcelona /ID# 278532

    Barcelona, 08036

    Recruiting
  • Hospital Universitario de Gran Canaria Doctor Negrin /ID# 278527

    Las Palmas de Gran Canaria, Las Palmas, 35010

    Recruiting
  • Complejo Asistencial Universitario de Leon - Hospital de Leon /ID# 278534

    León, 24071

    Recruiting
  • Hospital General Universitario Gregorio Maranon /ID# 278551

    Madrid, 28007

    Recruiting
  • Hospital Universitario Ramon y Cajal /ID# 278533

    Madrid, 28034

    Recruiting
  • Hospital Universitario 12 de Octubre /ID# 278520

    Madrid, 28041

    Recruiting
  • Clinica Universidad de Navarra - Pamplona /ID# 278583

    Pamplona, Navarre, 31008

    Recruiting
  • Hospital Universitario de Salamanca /ID# 278530

    Salamanca, 37007

    Recruiting
  • Hospital Universitario Marques de Valdecilla /ID# 278535

    Santander, Cantabria, 39008

    Recruiting
  • Complejo Hospitalario Universitario de Santiago /ID# 278531

    Santiago de Compostela, A Coruna, 15706

    Recruiting
  • Hospital Universitari i Politecnic La Fe /ID# 278525

    Valencia, 46026

    Recruiting

Other trials in Spain

Japan5 sites, 5 recruiting
  • Tokai University Hospital /ID# 278157

    Isehara, Kanagawa, 259-1193

    Recruiting
  • Kurume University Hospital /ID# 278209

    Kurume-shi, Fukuoka, 830-0011

    Recruiting
  • University Hospital Kyoto Prefectural University of Medicine /ID# 278156

    Kyoto, Kyoto, 602-8566

    Recruiting
  • Matsuyama Red Cross Hospital /ID# 278660

    Matsuyama, Ehime, 790-8524

    Recruiting
  • Nagoya City University Hospital /ID# 278188

    Nagoya, Aichi-ken, 467-8602

    Recruiting

Other trials in Japan

About this study

Official title: Phase 2/3, Multicenter, Randomized, Open-Label Study Evaluating the Efficacy and Safety of Etentamig and Daratumumab (Etentamig+D) Compared to Daratumumab, Lenalidomide, and Dexamethasone (DRd) in Subjects With Newly Diagnosed Multiple Myeloma Not Eligible for Transplant

Multiple myeloma (MM) is a cancer of the blood's plasma cells. The cancer is typically found in the bones and bone marrow (the spongy tissue inside of the bones) and can cause bone pain, fractures, infections, weaker bones, and kidney failure. This is a study to determine the adverse events, change in disease activity, and pharmacokinetics of Etentamig in adult participants with MM.

Etentamig is an investigational drug being developed for the treatment of MM. This study is broken into 2 phases; a phase 2 dose selection and optimization cohort with 3 study arms and a subcutaneous (SC) safety cohort with 2 study arms. Phase 3 participants will receive etentamig at recommended Phase 3 dose (RP3D). Around 680 adult participants with MM will be enrolled at approximately 155 sites worldwide

Read more

Participants in the phase 2 dose selection and optimization cohort will receive 1 of 3 doses of etentamig as intravenous (IV) infusions, combination with subcutaneous (SC) injections of daratumumab. The Phase 2 subcutaneous (SC) safety cohort participants will receive 1 of 2 doses of etentamig in combination with daratumumab. Participants in phase 3 will receive RP3D doses of etentamig as IV infusions, combination with SC injections of daratumumab, or SC injections of daratumumab, capsules of lenalidomide, and tablet/ IV injections of dexamethasone (DRd). The study duration is approximately 16 years.

There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and questionnaires.

Being tested
Etentamig, Lenalidomide, Daratumumab, Dexamethasone
Keywords
Multiple Myeloma, Etentamig, Daratumumab, Lenalidomide, Dexamethasone
Medical subject headings
Multiple Myeloma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07095452
Study groupRoleWhat they receive
Phase 2 Cohort 1: Etentamig + Daratumumab Dose AExperimentalParticipants will receive etentamig dose A in combination with daratumumab until the recommended phase 3 dose (RP3D), as part of the approximately 16 year study duration.
Receives: Drug: Etentamig; Drug: Daratumumab
Phase 2 Cohort 1: Etentamig + Daratumumab Dose BExperimentalParticipants will receive etentamig dose B in combination with daratumumab until the RP3D, as part of the approximately 16 year study duration.
Receives: Drug: Etentamig; Drug: Daratumumab
Phase 2 Cohort 1: Etentamig + Daratumumab Dose CExperimentalParticipants will receive etentamig dose C in combination with daratumumab until the RP3D, as part of the approximately 16 year study duration.
Receives: Drug: Etentamig; Drug: Daratumumab
Phase 2 Cohort 2: Etentamig + Daratumumab Dose AExperimentalParticipants will receive subcutaneous (SC) etentamig dose A in combination with daratumumab until the RP3D, as part of the approximately 16 year study duration.
Receives: Drug: Daratumumab; Drug: Etentamig
Phase 2 Cohort 2: Etentamig + Daratumumab Dose BExperimentalParticipants will receive subcutaneous (SC) etentamig dose B in combination with daratumumab until the RP3D, as part of the approximately 16 year study duration.
Receives: Drug: Daratumumab; Drug: Etentamig
Phase 3: Etentamig + Daratumumab RP3DExperimentalParticipants will receive etentamig at the RP3D in combination with daratumumab, as part of the approximately 16 year study duration.
Receives: Drug: Etentamig; Drug: Daratumumab
Phase 3: Daratumumab, Lenalidomide, and Dexamethasone (DRd)ExperimentalParticipants will receive DRd, as part of the approximately 16 year study duration.
Receives: Drug: Lenalidomide; Drug: Daratumumab; Drug: Dexamethasone

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Phase 2 and 3: Percentage of Participants with Adverse Events (AE)s

    An AE is defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment.

    Measured: Up to Approximately 16 Years

  2. Phase 2: Change in Clinical Activity

    Clinical activity is defined as change in response rates [Overall Response Rate (ORR), Complete Response (CR) or Better, Very Good Partial Response (VGPR), Partial Response (PR)] as determined International Myeloma Working Group (IMWG (2016).

    Measured: Up to Approximately 52 weeks

  3. Phase 3: Minimal Residual Disease (MRD) Negative CR Rate

    MRDnegCR rate, is defined as the percentage of participants who have achieved stringent complete response (sCR) or CR as assessed by independent review committee (IRC) and have negative MRD defined at 10^-5 threshold as assessed by next generation sequencing (NGS).

    Measured: Up to Approximately 52 weeks

  4. Phase 3: Progression-Free Survival (PFS)

    PFS is defined as the duration from the date of randomization to the date of confirmed disease progression (PD) determined by IRC per IMWG (2016) response criteria, or death, whichever occurs first.

    Measured: Up to Approximately 130 Months

Secondary outcomes (29)
  1. Phase 2: MRD Negative CR Rate

    MRDnegCR rate, is defined as the percentage of participants who have achieved sCR or CR and have negative MRD defined at 10^-5 threshold as assessed by NGS.

    Measured: Up to Approximately 52 Weeks

  2. Phase 2: PFS

    PFS is defined as the duration from the date of randomization to the date of confirmed disease progression (PD) determined by IRC per IMWG (2016) response criteria, or death, whichever occurs first.

    Measured: Up to Approximately 130 Months

  3. Phase 2: Sustained MRD Negativity Rate

    The rate of sustained MRD-negativity is defined as the percentage of participants with maintenance of MRD negativity status in bone marrow confirmed >=12 months apart prior to initiation of new anti-MM therapy.

    Measured: Up to Approximately 12 Months

  4. Phase 2: Area Under the Serum Concentration-Time Curve (AUC)

    Area under the plasma concentration-time curve (AUC).

    Measured: Up to Approximately 12 Months

  5. Phase 2: Overall Survival (OS)

    OS is defined as the duration from the date of randomization to the date of the participant's death.

    Measured: Up to Approximately 16 Years

  6. Phase 2: Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability

    Incidence, severity, seriousness, and causality of treatment-emergent adverse events (TEAEs)

    Measured: Up to Approximately 16 Years

  7. Phase 2: Maximum Observed Serum Concentration (Cmax)

    Maximum observed serum concentration (Cmax).

    Measured: Up to Approximately 12 Months

  8. Phase 2: Time to Cmax (Time to Maximum Observed Concentration, Tmax)

    Time to Cmax.

    Measured: Up to Approximately 12 Months

  9. Phase 2: Positive Anti-Drug Antibodies (ADAs)

    Positive ADAs.

    Measured: Up to Approximately 90 days after the last dose of study treatment

  10. Phase 2: Negative ADAs

    Negative ADAs.

    Measured: Up to Approximately 90 days after the last dose of study treatment

  11. Phase 2: Neutralizing Anti-Drug Antibodies (NAbs)

    Neutralizing anti-drug antibodies (NAbs).

    Measured: Up to Approximately 90 days after the last dose of study treatment

  12. Phase 3: OS

    OS is defined as the duration from the date of randomization to the date of the participant's death.

    Measured: Up to Approximately 16 Years

  13. Phase 3: Sustained MRD Negativity Rate

    The rate of sustained MRD-negativity is defined as the percentage of participants with maintenance of MRD negativity status in bone marrow confirmed >=12 months apart prior to initiation of new anti-MM therapy.

    Measured: Up to Approximately 12 Months

  14. Phase 3: Rate of >= CR

    The rate of >= CR is defined as the percentage of participants who achieve a sCR or CR determined by IMWG (2016) response criteria, per IRC assessment, prior to the initiation of new anti-myeloma therapy.

    Measured: Up to Approximately 12 Months

  15. Phase 3: Rate of >= VGPR or Better

    The rate of >= VGPR is defined as the percentage of participants who achieve a VGPR or better determined by IMWG (2016) response criteria, per IRC assessment, prior to the initiation of new anti-myeloma therapy.

    Measured: Up to Approximately 12 Months

  16. Phase 3: ORR

    ORR is defined as percentage of participants with a response of PR or better per IMWG criteria.

    Measured: Up to Approximately 52 Weeks

  17. Phase 3: Time to Response (TTR)

    TTR is defined as the number of months from the date of randomization to the date of best overall response of CR or PR ('responders') determined by IMWG criteria as assessed by investigator.

    Measured: Up to Approximately 12 Months

  18. Phase 3: Duration of Response (DOR)

    DOR is defined as the number of days from the day the response criteria are met to the date that disease progression.

    Measured: Up to Approximately 16 Years

  19. Phase 3: Time-to-Progression (TTP)

    Time to progression is defined as the number of days from the date of randomization to the date of the first documented disease progression or relapse.

    Measured: Up to Approximately 16 Years

  20. Phase 3: Event Free Survival (EFS)

    EFS will be measured as the number of days between the initiation of the subsequent anticancer therapy and disease progression, or refractory disease, or death.

    Measured: Up to Approximately 16 Years

  21. Phase 3: Progression-Free Survival on Subsequent Therapy (PFS2)

    PFS2 is defined as the duration from the date of randomization to the date of confirmed disease progression on the next line of therapy or death, whichever occurs first

    Measured: Up to Approximately 16 Years

  22. Phase 3: Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability

    Incidence, severity, seriousness, and causality of TEAEs

    Measured: Up to Approximately 16 Years

  23. Phase 3: Change from Baseline in European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) Physical Functioning Score

    The EORTC QLQ-C30 is a 30-item patient-reported questionnaire composed of both multi-item and single scales including 5 functional scales (physical, role, emotional, social, and cognitive), 3 symptom scales (fatigue, nausea and vomiting, and pain), a global health status/QoL scale, and 6 single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). Subjects rate items on a 4- point scale ranging from 1 to 4 (1 = Not at All, 2 = A Little, 3 = Quite a Bit, and 4 = Very Much).

    Measured: Up to Approximately 16 Years

  24. Phase 3: Change from Baseline in EORTC QLQ-C30 Global Health Status/QoL Score

    The EORTC QLQ-C30 is a 30-item patient-reported questionnaire composed of both multi-item and single scales including 5 functional scales (physical, role, emotional, social, and cognitive), 3 symptom scales (fatigue, nausea and vomiting, and pain), a global health status/QoL scale, and 6 single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). Subjects rate items on a 4- point scale ranging from 1 to 4 (1 = Not at All, 2 = A Little, 3 = Quite a Bit, and 4 = Very Much).

    Measured: Up to Approximately 16 Years

  25. Phase 3: Change from Baseline and Time to Deterioration in the Remaining Scales and Items of EORTC QLQ-C30

    The EORTC QLQ-C30 is a 30-item patient-reported questionnaire composed of both multi-item and single scales including 5 functional scales (physical, role, emotional, social, and cognitive), 3 symptom scales (fatigue, nausea and vomiting, and pain), a global health status/QoL scale, and 6 single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). Subjects rate items on a 4- point scale ranging from 1 to 4 (1 = Not at All, 2 = A Little, 3 = Quite a Bit, and 4 = Very Much).

    Measured: Up to Approximately 16 Years

  26. Phase 3: Symptomatic AEs as Assessed by the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

    PRO-CTCAE includes 124 items representing 78 symptomatic toxicities drawn from the CTCAE. PRO-CTCAE items evaluate the symptom attributes of frequency, severity, interference, amount, presence/absence. All questions employ a 7-day recall period and are scored from 0 to 4 (or 0/1 for absent/present).

    Measured: Up to Approximately 16 Years

  27. Phase 3: Overall Bother Due to Treatment Side Effects as Assessed by the Functional Assessment of Cancer Therapy-General (FACT-G) GP5

    The FACT-G GP5 Item is a part of the FACT-G which is a 27-item questionnaire that measures four domains of health-related quality of life (HRQOL) in cancer patients: physical, social, emotional and functional well-being. The FACT-G GP5 item ("I am bothered by side effects of treatment") is used to assess overall treatment tolerability in patients by assessing the overall side effect impact on patients. This item is rated on a 5-point Likert scale from "not at all" to "very much.".

    Measured: Up to Approximately 16 Years

  28. Phase 3: Change from Baseline in Patient Global Impression of Severity (PGIS) Scores

    The PGIS scale asks the patient to assess their overall QoL, as well as difficulty of doing physical activities due to MM over the past 7 days. Each item employs a 5-point Likert scale from "not at all" to "very much."

    Measured: Up to Approximately 16 Years

  29. Phase 3: Change from Baseline in European Quality of Life 5 Dimensions (EQ-5D-5L) Scores

    The EQ-5D descriptive system comprises 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems, and extreme problems.

    Measured: Up to Approximately 16 Years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Jul 2025
  2. Study start8 Jan 2026
  3. Primary completionMar 2041 (estimated)
  4. Study completionJan 2042 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Sequential
Masking
None (open label)
Enrolment
680 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07095452
Sponsor's protocol ID
M25-586
Other IDs
2025-520897-21, 2025-520897-21-00, 2025
Status last verified
Oct 2026
First submitted
24 Jul 2025
Last updated
19 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: AbbVie is committed to responsible clinical trial data sharing. This includes access to anonymized, individual and trial-level data (analysis data sets), as well as other information.

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