Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06413498 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study of Multiple Myeloma, sponsored by Kite, A Gilead Company.

Recruiting
Registry status
Phase 3
Development phase
450
Enrollment target
20
Study locations

NCT06413498: Recruiting Phase 3 study of Multiple Myeloma, sponsored by Kite, A Gilead Company.

NCT06413498 is a Phase 3 study of Multiple Myeloma that is actively recruiting participants, run by Kite, A Gilead Company. The registered enrollment target is 450 participants, below the 546-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (18% lower). The trial reports 20 study locations across 10 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT06413498, a Phase 3 study of Multiple Myeloma, is actively recruiting participants, sponsored by Kite, A Gilead Company.

RECRUITING
Registry status
Phase 3
Development phase
450 participants
Enrollment target
20
Study locations

Study Summary

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.

Primary Outcome

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.

Conditions Studied

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • DRUG Pomalidomide
  • DRUG Bortezomib
  • DRUG Anitocabtagene Autoleucel

Study Locations (20)

California

  • City of Hope (City of Hope National Medical Center, City of Hope Medical Center) - Duarte
  • USC/Norris Comprehensive Cancer Center - Los Angeles
  • University of California Davis Comprehensive Cancer Center - Sacramento
  • UC San Diego Moores Cancer Center - San Diego
  • University of California San Francisco Medical Center - San Francisco
  • UCLA Hematology/Oncology (Bowyer Infusion Clinic) - Santa Monica
  • Stanford Cancer Institute - Stanford

Florida

  • Sylvester Comprehensive Cancer Center - Coral Gables
  • Mayo Clinic - Jacksonville
  • Moffitt Cancer Center - Tampa

Arizona

  • Banner MD Anderson Cancer Center - Gilbert
  • Mayo Clinic Hospital - Gilbert

Georgia

  • Winship Cancer Institute, Emory University - Atlanta
  • Southeastern Regional Medical Center, Inc. dba City of Hope Atlanta - Newnan

Colorado

  • Colorado Blood Cancer Institute - Denver

Idaho

  • St. Luke's Cancer Institute - Boise

Illinois

  • University of Illinois Hospital and Health Sciences System - Chicago

Indiana

  • IU Melvin and Bren Simon Comprehensive Cancer Center - Indianapolis

Trial Details

FieldValue
Enrollment Target 450 participants
Start Date 2024-08-23
Est. Completion 2031-07
Phase Phase 3
Kite, A Gilead Company

28 total trials

What NCT06413498 shows while recruiting

NCT06413498 is an interventional study that assigns participants to a tested intervention. The registered 450 participants enrollment target is mid-sized for trials with a published cap, below the 546-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (18% lower).

The record links to 1 condition, with Multiple Myeloma appearing as the primary indexed condition, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT06413498 names 20 study sites across 10 states, led by California, Florida, Arizona.

Frequently Asked Questions

What is clinical trial NCT06413498 about?

NCT06413498 is a clinical study titled "A Study Comparing Anitocabtagene Autoleucel to Standard of Care Therapy in Participants With Relapsed/ Refractory Multiple Myeloma". 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...

What is the current status of trial NCT06413498?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 450 participants. The study started on 2024-08-23. Estimated completion is 2031-07.

What conditions does trial NCT06413498 study?

This clinical trial studies the following conditions: Multiple Myeloma.

What interventions are being tested in trial NCT06413498?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), Pomalidomide (DRUG), Bortezomib (DRUG), Anitocabtagene Autoleucel (DRUG).

Who is sponsoring clinical trial NCT06413498?

This trial is sponsored by Kite, A Gilead Company, which has 28 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06413498 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Multiple Myeloma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06413498's enrollment target sits among peer trials

450 52nd of 438 higher than 385 of 438 other Multiple Myeloma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Multiple Myeloma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00515060 · 450 participants

    Psychophysical Studies of Cancer Therapy Pain

  • NCT01257269 · 450 participants

    Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)

  • NCT03047161 · 450 participants

    Electrophysiology of Fetal Arrhythmia

  • NCT03269630 · 450 participants

    New Orleans Pulmonary Hypertension Biobank

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06413498, the US trial registry maintained by the National Library of Medicine. NCT06413498 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.