Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06158841

Study Assessing Activity of Intravenous (IV) Etentamig Monotherapy Versus Standard Available Therapies in Adult Participants With Relapsed or Refractory Multiple Myeloma

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. Treatments are available, but MM can come back (relapsed) or may not get better (refractory) with treatment. This is a study to determine change in disease symptoms of etentamig compared to standard available therapies in adult participants with relapsed/refractory (R/R) MM.

Etentamig is an investigational drug being developed for the treatment of R/R MM. This study is broken into 2 Arms; Arm A and Arm B. In Arm A, participants will receive etentamig as a monotherapy. In Arm B, participants will receive the standard available therapy (SAT) identified by the Investigator during screening, in accordance with the local (or applicable) approved label, package insert, summary of product characteristics, and/or the institutional guidelines, as applicable. Around 380 adult participants with relapsed/refractory multiple myeloma will be enrolled at approximately 140 sites across the world.

In Arm A participants will receive etentamig as an infusion into the vein in 28 day cycles, during the 3.5 year study duration. In Arm B, participants will receive the SAT identified by the Investigator during screening, in accordance with the local (or applicable) approved label, package insert, summary of product characteristics, and/or the institutional guidelines, as applicable, during the 3.5 year study duration.

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

St George Hospital - Kogarah /ID# 261806, Kogarah, New South Wales, Australia

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Eastern Cooperative Oncology Group (ECOG) performance of <= 2.
  • Diagnosis of relapsed/refractory (R/R) multiple myeloma (MM) during or after the participant's last treatment as stated in the protocol.
  • Must have measurable disease with at least 1 of the following assessed within 28 days of enrollment:
  • Serum M-protein >= 0.5 g/dL (>= 5 g/L).
  • Urine M-protein >= 200 mg/24 hours.
  • In participants without measurable serum or urine M protein, serum free light chain (FLC) >= 100 mg/L (10 mg/dL) (involved light chain)and an abnormal serum kappa lambda ratio.
  • Must have received at least 2 or more lines of therapy, including a proteasome inhibitor (PI), an immunomodulatory imide (IMiD), and an anti-CD38 monoclonal antibody (mAb).

-- US and Puerto Rico only: Participant must have received at least 1 or more line of therapy, including exposure to a PI, an IMiD, and an anti-CD38 mAb.

  • Must be eligible to receive the Investigator's choice standard available therapy (SAT) based on approved prescribing information, previous MM treatment history, and institutional guidelines.

Exclusion criteria

  • Clinically significant (per Investigator's judgment) drug or alcohol abuse within the last 6 months.
  • Clinically significant conditions such as but not limited to the following: neurologic, psychiatric, endocrine, metabolic, immunologic, cardiovascular, pulmonary, or hepatic disease within the last 6 months that would adversely affect the participant's participation in the study.
  • Central nervous system involvement of MM.
  • Has received B-cell maturation antigen (BCMA)-targeted therapy.

Treatment and study plan

Etentamig

Drug

Intravenous (IV) Infusion

Other names: ABBV-383

Carfilzomib

Drug

IV Infusion

Pomalidomide

Drug

Oral Capsule

Elotuzumab

Drug

IV Infusion

Selinexor

Drug

Oral Tablet

bortezomib

Drug

Subcutaneous or IV Injection

Dexamethasone

Drug

Oral Tablet or IV Infusion

Primary outcomes

  1. Progression Free Survival (PFS)

    Time frame: Up to Approximately 5 Years

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

  2. Objective Response Rate (ORR)

    Time frame: Up to Approximately 5 Years

    ORR is defined as the percentage of participants who achieve confirmed partial response (PR) + VGPR + complete response (CR) + stringent complete response (sCR) or per IRC assessment.

Secondary outcomes

  1. Overall Survival (OS)

    Time frame: Up to Approximately 5 Years

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

  2. Change in Rate of Very Good Partial Response (VGPR) or Better (>= VGPR)

    Time frame: Up to Approximately 5 Years

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

  3. Change in Rate of CR or Better (>=CR)

    Time frame: Up to Approximately 5 Years

    >=CR is defined as the percentage of participants who achieve confirmed CR + sCR or per IRC assessment.

  4. Change in Rate of Minimum Residual Disease (MRD) negativity with >= CR

    Time frame: Up to Approximately 5 Years

    MRD negativity with >= CR, defined as achievement of CR or better by IMWG (2016) response criteria (per IRC assessment) and MRD negative status as assessed by next-generation sequencing (NGS) Adaptive Clonoseq at 10^-5 threshold.

  5. Change from Baseline in Disease Symptoms as Measured by the Disease Symptoms Domain of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Multiple Myeloma Module (EORTC QLQ-MY20)

    Time frame: Up to 6 Months

    The disease symptoms domain of EORTC QLQ-MY20 is a 6-item questionnaire to assess the physical function of the participant, with a higher score indicating a higher level of symptoms.

  6. Change from Baseline in Physical Functioning as Measured by the Physical Functioning Domain of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30 (EORTC QLQ-C30)

    Time frame: Up to 6 Months

    The physical functioning domain of EORTC QLQ-C30 is a 5-item questionnaire to assess the physical function of the participant, with a higher score indicating worse functioning.

  7. Time to Response (TTR)

    Time frame: Up to Approximately 5 Years

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

  8. Duration of Response (DOR)

    Time frame: Up to Approximately 5 Years

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

  9. Time-to-Progression (TTP)

    Time frame: Up to Approximately 5 Years

    TTP is defined as the number of days from the date of first dose to the date of earliest disease progression as determined by the IRC.

  10. Time to Next Anti-lymphoma Therapy (TTNT)

    Time frame: Up to Approximately 5 Years

    TTNT is defined as the time from randomization to first documented administration of subsequent anti-lymphoma therapy.

  11. Number of Participants with Event-free Survival (EFS)

    Time frame: Up to Approximately 5 Years

    EFS is defined as the time from randomization until adverse event determined by the IRC, or death, whichever occurs first.

  12. Change from Baseline in Patient-Reported Outcomes Measurement Information System Fatigue Short Form 7a (PROMIS Fatigue SF 7a)

    Time frame: Up to Approximately 6 Months

    The PROMIS Fatigue SF7a is a 7-item short form that assesses the impact and experience of fatigue in the past 7 days. For each item, 5-point rating scales are used to measure frequency ("Never," "Rarely," "Sometimes," "Often," or "Always") with a higher score indicating a greater impact.

  13. Change from Baseline in Patient Reported Outcomes-Common Terminology Criteria for Adverse Events (PRO-CTCAE)

    Time frame: Up to Approximately 6 Months

    The PRO-CTCAE is a patient-reported outcome measurement system developed to assess symptomatic toxicity in participants in cancer clinical trials. PRO-CTCAE items are scored from 0 to 4 to evaluate common symptoms from study treatment on their frequency, severity, interference, amount, presence/absence.

  14. Change from Baseline in Remaining Items in the EORTC QLQ-C30

    Time frame: Up to Approximately 6 Months

    The EORTC QLQ-C30 assesses health-related quality of life in cancer patients participating in clinical trials. The EORTC QLQ-C30 comprises 5 functional scales (physical, role, emotional, social, cognitive), 8 single-item symptom scales (fatigue, pain, nausea/vomiting, appetite loss, constipation, diarrhea, insomnia, and dyspnea), as well as subscales assessing global health/quality of life and financial impact. Raw scores are transformed to a scale of 0 to 100, with higher scores representing better functioning/quality of life and greater symptom burden.

  15. Change from Baseline in Remaining Items in the EORTC QLQ-MY20

    Time frame: Up to Approximately 6 Months

    The EORTC QLQ-MY20 consists of four scales: two symptom scales (Disease Symptoms [6 items] and Side Effects of Treatment [10 items]), one function scale (Future Perspective [3 items]), and one single item (Body Image). Each item has four response options: "Not at all," "A little," "Quite a bit," or "Very much". All scores are then linearly transformed to a 0 to 100 scale. A higher score on the symptom scales indicates a higher level of symptoms, whereas higher scores on future perspective and body image indicate good functioning or support.

  16. Change from Baseline in European Quality-of-Life 5-dimensional-5-level (EQ-5D-5L)

    Time frame: Up to Approximately 6 Months

    The EQ-5D-5L is a standardized, non-disease specific instrument used to measure health-related quality of life. The EQ-5D-5L assesses general health on 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). The scores for the 5 dimensions are used to compute a single utility index score ranging from 0 to 1 representing the general health status of the individual, with higher scores indicating better health state.

  17. Change from Baseline in Patient Global Impression of Severity (PGIS)

    Time frame: Up to Approximately 6 Months

    The self-report measure PGIS reflects a participant's belief about their lymphoma symptoms over the past 7 days. The PGIS is a 5-point scale depicting a participant's rating of overall severity.

  18. Change from Baseline in Patient Global Impression of Change (PGIC)

    Time frame: Up to Approximately 6 Months

    The self-report measure PGIC reflects a participant's belief about the efficacy of treatment. The PGIC is a 7-point scale depicting a participant's rating of overall improvement since start of treatment. Participants rate their change as very much improved, much improved, minimally improved, no change, minimally worse, much worse, or very much worse.

  19. Number of Participants with Skeletal-Related Event (SRE)

    Time frame: Up to Approximately 5 Years

    SREs are defined as the presence of any of the following spinal cord compression, pathologic fracture, surgery to bone, or radiation to bone.

Study contacts

Contact information is provided by the study sponsor or research team.

ABBVIE CALL CENTER

CONTACT

[email protected]

844-663-3742

Sponsors and collaborators

Lead sponsor

AbbVie

Industry

Registry information

Official study title

A Phase 3, Multicenter, Randomized, Open Label Study of Etentamig Compared With Standard Available Therapies in Subjects With Relapsed or Refractory Multiple Myeloma (3L+ RRMM Monotherapy Study)

Acronym: CERVINO

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Dec 6, 2023
Registry last updated
Jul 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.