Phase 3 Myeloma Trial, Recruiting NCT07391657 Sponsor: AstraZeneca Condition: Myeloma
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Phase 3 Myeloma Trial, Recruiting

NCT07391657
Recruiting Phase 3 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are 18 years old or older
  • You have been formally diagnosed with multiple myeloma based on recognised diagnostic standards
  • Your myeloma can be measured through specific blood or urine tests showing certain protein levels above set thresholds (confirm with trial site)
  • Your myeloma has gotten worse during or after your most recent treatment, and if you have only had one previous treatment, your disease must have progressed within a specific time window after a stem cell transplant or after starting initial therapy (confirm with trial site)
  • You have received between 1 and 3 previous lines of treatment, including specific types of myeloma drugs known as an IMiD and either a PI or a CD38 antibody, with at least 2 full cycles completed for each line unless your disease got worse right away
  • You are eligible to receive at least one of four specific standard treatment combinations as decided by the trial doctor (confirm with trial site)
  • You are generally well enough to carry out light daily activities with no or minimal limitations (a score of 0 or 1 on a standard health scale)
  • Your blood counts and organ function (including blood cells, liver, and kidneys) meet minimum health thresholds as shown by recent lab tests (confirm with trial site)

Who may not be able to join:

  • Your myeloma has spread to the brain or spinal fluid, or you have signs of this
  • You have been diagnosed with certain related blood or protein disorders, such as primary amyloidosis, plasma cell leukaemia, Waldenstrom macroglobulinemia, or POEMS syndrome
  • Your myeloma never responded to any previous treatment at all
  • You have a significant neurological or psychiatric condition
  • You have another serious medical condition that could put you at unacceptable risk from the trial treatment
  • You have previously received any treatment that targets a protein called BCMA
  • You have previously received a type of immune cell therapy called CAR-T or CAR-NK therapy
  • You have previously received a type of therapy called a T-cell engager
  • You received a donor stem cell transplant at any point, or received your own stem cell transplant within 12 weeks of joining the trial

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 20 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 1-877-240-9479

Australian sites

Research Site, Camperdown,
Research Site, Darlinghurst,
Research Site, Fitzroy,
Research Site, Liverpool,
Research Site, Melbourne,
Research Site, Melbourne,
Research Site, Murdoch,

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Registry
ClinicalTrials.gov
Start date
23 February 2026
Est. completion
14 June 2028

Where this trial is recruiting

🇦🇺 Australia 🇧🇷 Brazil 🇨🇦 Canada 🇨🇳 China 🇫🇷 France 🇩🇪 Germany 🇮🇹 Italy 🇯🇵 Japan 🇳🇴 Norway 🇵🇱 Poland 🇰🇷 South Korea 🇪🇸 Spain 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

7 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

To demonstrate the superiority of AZD0120 relative to standard therapy (DKd, DPd, PVd, or Kd) by assessment of PFS in participants with RRMM.; To demonstrate the superiority of AZD0120 relative to standard therapy (DKd, DPd, PVd, or Kd) by assessment of MRD negativity rate at 9 months in participants with RRMM.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov