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Next-Gen Dual-Target CAR-T Trial for Relapsed and Refractory Multiple Myeloma

To refer a patient for trial eligibility, please submit a referral form or contact the Moffitt clinical trial coordinator for MCC23586.

Key Highlights

  • 100% ORR in early data (evaluable patients)
  • No Grade ≥3 CRS or ICANS observed
  • Dual-targeting (BCMA + CD19)
  • Faster manufacturing timeline (about 14 days)

Designed for patients who have received at least 3 prior lines, including PI, IMiD, and anti-CD38 therapy.

Next Generation CAR-T Therapy Clinical Trial #23586

Refer eligible patients for a Phase 1b/2 study evaluating AZD0120 (BCMA/CD19 CAR-T) with early signals of deep response and favorable safety.

A Potential Next Step for Unresponsive Myeloma Patients

Patients with RRMM who have progressed after standard therapies often face limited options. AZD0120 is designed to:

  • Target two antigens (BCMA + CD19) to reduce tumor escape
  • Deliver rapid and deep responses
  • Maintain a manageable safety profile

Early Clinical Results Show Promise

Results from Phase 1b. Highlights below or read the published study

Efficacy

  • ORR: 100% (n=15 evaluable)
  • 33% sCR / 47% VGPR
  • 100% MRD negativity (evaluable pts)
  • Median time to response: about 1 month

Safety

  • No Grade ≥3 CRS
  • No ICANS observed
  • CRS mostly Grade 1–2, short duration (about 2 days)

Operational Advantage

  • Manufacturing: about 14 days
  • Vein-to-vein: about 28 days
  • Utilizes FasTCAR Technology

Note: Data is early phase with limited follow-up. ORR (Overall Response Rate), sCR (Stringent Complete Response), VGPR (Very Good Partial Response), MRD negativity (Minimal or Measurable Residual Disease negativity), CRS (Cytokine Release Syndrome), ICANS (Immune Effector Cell-Associated Neurotoxicity Syndrome), 

Which Patients May Be Eligible?

Inclusion Criteria Summary:

  • Relapsed/refractory multiple myeloma
  • ≥3 prior lines of therapy
  • Prior PI + IMiD + anti-CD38
  • ECOG 0–1
  • Adequate organ function

Exclusion Criteria Summary:

  • Active CNS involvement
  • Significant cardiac disease
  • Recent stem cell transplant

Review full clinical trial details

Not sure if your patient qualifies? Contact a Clinical Research Coordinator for rapid eligibility review: Garrett.Welch@moffitt.org 

What does trial participation look like for patients?

  1. Submit referral request and send patient records to Moffitt
  2. Patients will be pre-screened for basic eligibility by the clinical research coordinator
  3. Initial appointment with Dr. Hansen
  4. Workup and clinical screening appointments
  5. Following enrollment in the trial, patient is scheduled for apheresis and chemotherapy
  6. Apheresis (cell collection) is a half-day appointment at Magnolia Campus
  7. Collected cells are sent for manufacturing (about two weeks). Patients usually remain at home during cell manufacturing process
  8. Patient receives infusion of cells at Magnolia Campus

The patient and their caregiver will need to remain within 1 hour of Moffitt's Magnolia Campus for about 28 days after infusion of cells, for careful monitoring and multiple visits. The trial sponsor will reimburse travel expenses and our team can support with finding accomodations for patients who live further away. 

  • a road

    Expenses Reimbursed

    Travel, lodging and meals expenses are covered by the trial sponsor from the first visit/screening through the 2 year follow up period via reimbursement

  • Hospital with a person

    Follow-up Care

    There are 2 years of active follow-up care. This is followed up by care visits every 6 months until 15 years post therapy.

Partner with Moffitt

A referral for a clinical trial means we will work together to give your patient the best chance at beating their cancer. 

For patients with RRMM who have exhausted standard options, this dual-target CAR-T approach represents a promising next step. We are encouraged by the early depth of response and the manageable profile observed to date.
Doris Hansen, MD
Principal Investigator

 

Have a patient you think would be a candidate for this clinical trial?

We are here to help, you can start a referral by submitting this online form. 

If you have questions for the Research Coordinator about the trial, please contact Garrett.Welch@moffitt.org.

For questions about referring your patient or to learn more about Moffitt you can speak with a Physician Liaison:

Contact Your Physician Liaison

Clinical Trial Referral Form

Patient Information

Patient Insurance Information

Is the patient the policy holder?
Policy Holder's Gender
Does the patient have secondary insurance?

Patient Health & Appointment Information

Why is this patient being referred to Moffitt?
Does the patient have a preferred Moffitt location?

Referring Provider Information

If a doctor or nurse practitioner referred you to this trial, please enter as much of their information below as you can. You can enter "N/A" for any unknown fields

If a doctor or nurse practitioner referred you to this trial, please enter as much of their information below as you can. You can enter "N/A" for any unknown fields

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