A Study Comparing Anitocabtagene Autoleucel to Standard of Care Therapy in Participants With Relapsed/ Refractory Multiple Myeloma

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorKite, A Gilead Company

About this trial

The goal of this study (iMMagine-3) is to compare the study drug, anitocabtagene autoleucel to standard of care therapy (SOCT) in participants with relapsed/refractory multiple myeloma who have received 1 to 3 prior lines of therapy, including an anti-CD38 monoclonal antibody and an immunomodulatory drug.

The primary objective of this study is to compare the efficacy of anitocabtagene autoleucel versus SOCT in participants with RRMM.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Documented historical diagnosis of multiple myeloma (MM)

Received 1 to 3 prior lines of antimyeloma therapy, including an immunomodulatory drug (IMiD) and an anti-cluster of differentiation 38 (CD38) monoclonal antibody (mAb). A minimum of 2 consecutive cycles of an IMiD and an anti-CD38 mAb in any prior line of therapy is required. The IMiD and anti-CD38 mAb do not need to be from the same regimen in the prior line(s) of therapy.

Documented evidence of progressive disease by IMWG criteria based on the investigator's determination on or within 12 months of the last dose of the last regimen

Serum M-protein level ≥ 0.5 g/dL or urine M-protein level ≥ 200 mg/24 hours; or

Disqualifiers

Prior B-cell maturation antigen (BCMA)-targeted therapy

Prior T-cell engager therapy

Prior CAR therapy or other genetically modified T-cell therapy

Active or prior history of central nervous system (CNS) or meningeal involvement of MM

Trial design

Design model

Parallel

Treatments tested in this trial

  • Anitocabtagene Autoleucel

    Drug

    A single infusion of CAR+ transduced autologous T cells

  • Cyclophosphamide

    Drug

    Administered intravenously

  • Fludarabine

    Drug

    Administered intravenously

  • Pomalidomide

    Drug

    Tablet administered orally

  • Bortezomib

    Drug

    Administered intravenously or subcutaneously

  • Dexamethasone

    Drug

    Tablet administered orally

  • Daratumumab

    Drug

    Administered intravenously or subcutaneously

  • Carfilzomib

    Drug

    Administered intravenously

Treatment groups

450 Participants
are divided into 2 treatment groups
Group A: Anitocabtagene AutoleucelExperimental treatment 3 interventions
Group B: Standard of Care Therapy (SOCT)Active comparator 5 interventions

Trial outcomes

Primary outcomes

1

Progression-Free Survival (PFS)

PFS is defined as the time from randomization to disease progression per International Myeloma Working Group (IMWG) criteria as determined by independent review committee (IRC), or death due to any cause, whichever occurs first.

Time frame
Up to 4 years
2

Minimal Residual Disease (MRD) Complete Response (CR) Rate at 9 Months

Minimal MRD is defined as the proportion of participants achieving CR/stringent CR (sCR) and MRD-negative status at 9 months. MRD negativity at 9 months is defined as negative MRD value at 9 months (± 3 months) in bone marrow assessment (\< 1 in 105 nucleated cells per IMWG criteria using NGS) (Kumar 2016). CR/sCR per IMWG criteria is determined by IRC.

Time frame
Up to 9 months

Secondary outcomes

1

CR Rate (CR/ Stringent Complete Response (sCR))

CR rate is defined as the proportion of participants who achieved a best overall response of CR or sCR per IMWG criteria as determined by IRC.

Time frame
Up to 4 years
2

Overall MRD Negativity

Overall MRD negativity, defined as the proportion of any MRD negativity in participants with bone marrow aspirate (\< 1 in 10\^5 nucleated cells per IMWG criteria using next-generation sequencing (NGS)) at any time after randomization until disease progression, subsequent anti-multiple myeloma (MM) therapy, or death.

Time frame
Up to 7 years
3

Overall survival (OS)

OS is defined as the time from randomization to death due to any cause.

Time frame
Up to 7 years
4

Overall Response Rate (ORR)

ORR is defined as the proportion of participants who achieve a best overall response of at least partial response (PR) or better (sCR, CR, very good partial response (VGPR), or PR) per IMWG criteria.

Time frame
Up to 7 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Kite, A Gilead Company

Lead sponsor

Arcellx, Inc.

Collaborator