A Phase III, Multicentre Study to Evaluate Consolidation Treatment With AZD0120 Compared With ASCT, in Participants With Newly Diagnosed Multiple Myeloma Who Are Transplant Eligible (DURGA-6).

Starting soon · Phase 3

Conditions studied: Newly Diagnosed Multiple Myeloma (NDMM)

In brief

The purpose of this study is to measure the efficacy of AZD0120 compared with ASCT in terms of progression-free survival (PFS) according to the International Myeloma Working Group (IMWG) criteria 2016, and MRD negative complete response (CR) rate at 9 months as assessed by Blinded Independent Central Review (BICR), in participants with TE NDMM. Study details include: * The study duration is estimated to be up to 13 years from the date the first participant is randomised. * For participants in Arm A (AZD0120), the total duration of participant follow-up will be 15 years (including a Long Term Follow-up study) after the last participant has received the AZD0120 infusion. * The treatment duration will be:- Arm A (AZD0120): lymphodepletion over 3 days, a single-day infusion of AZD0120, followed by a maximum of 2 years lenalidomide monotherapy maintenance treatment. * Arm B (ASCT): conditioning therapy over 24 to 48 hours, ASCT, followed by a maximum of 2 years lenalidomide monotherapy maintenance treatment. Disclosure Statement: This is an open-label, randomised study with 2 treatment arms.

Key facts

Study ID: NCT07735637
Run by: AstraZeneca
People needed: 750
Starts: 2026-08-25
Expected to finish: 2039-11-09
Last updated by the study team: 2026-07-30

Who can join

Age: 18 and older, up to 130. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

≥18 years of age.
Documented diagnosis of NDMM according to IMWG diagnostic criteria.
Documented measurable disease at diagnosis (serum M-protein ≥ 1.0 g/dL, urine M-protein 200 mg/24 hour, or serum Ig FLC 10 mg/dL (100 mg/L) and abnormal serum Ig kappa lambda FLC ratio)
Must have completed 4 to 6 cycles of induction therapy with any of the following approved regimens: anti-CD38+VRd, DVTd, DRd or VRd
Participant must have at least SD or better per IMWG response criteria (2016) after completion of induction, and prior to randomisation.
ECOG performance status score of 0 or 1.
Eligible for treatment with high-dose melphalan (200 mg/m²) followed by ASCT.
Adequate organ and bone marrow function.

You may not qualify if…

Known active, or prior history of CNS involvement or exhibits clinical signs of meningeal involvement of MM.
Primary amyloidosis, active plasma cell leukaemia (at diagnosis and/or at time of screening), Waldenstrom macroglobulinemia or POEMS syndrome.
Significant neurological or psychiatric condition
Significant medical condition that places the participant at an unacceptable risk for treatment-related complications
Participants who required the introduction of an additional agent therapy due to inadequate response.
Prior T-cell engager therapy directed at any target.
Prior CAR-T and/or CAR-NK cell therapy directed at any target for any indications
Prior any therapy that is targeted to BCMA and CD19.

Where it is running

Research Site — Aarhus, Denmark
Research Site — København Ø, Denmark
Research Site — Odense, Denmark
Research Site — Lille, France
Research Site — Nantes, France
Research Site — Paris, France
Research Site — Paris, France
Research Site — Toulouse, France
Research Site — Berlin, Germany
Research Site — Dresden, Germany
Research Site — Essen, Germany
Research Site — Freiburg im Breisgau, Germany
Research Site — Hamburg, Germany
Research Site — Leipzig, Germany
Research Site — München, Germany
Research Site — Oldenburg, Germany
Research Site — Bologna, Italy
Research Site — Milan, Italy
Research Site — Milan, Italy
Research Site — Rome, Italy
Research Site — Rozzano, Italy
Research Site — Torino, Italy
Research Site — Oslo, Norway
Research Site — Gdansk, Poland
Research Site — Calgary, Alberta, Canada

Full record on ClinicalTrials.gov

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