Phase 3 Myeloma Trial, Recruiting NCT06152575 Sponsor: Pfizer Condition: Myeloma
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Phase 3 Myeloma Trial, Recruiting

NCT06152575
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:

  • People who have previously been diagnosed with multiple myeloma and have already received between 1 and 4 rounds of treatment, including a type of drug that targets a protein called CD38 and a drug called lenalidomide.
  • People whose myeloma has started growing again or did not respond to their most recent treatment.
  • People whose myeloma can be measured through specific blood or urine tests showing certain protein levels above defined thresholds (confirm with trial site for exact values).
  • People whose recent blood test results fall within the ranges required by the trial (confirm with trial site for exact values).
  • People who are reasonably well and able to carry out daily activities, based on a standard medical fitness scale — broadly, those who are fully active or have only mild limitations.
  • People who are not pregnant or breastfeeding, and who are willing to use contraception during the trial.

Who may not be able to join:

  • People who have a slow-growing, early form of myeloma that has not yet required treatment (smoldering multiple myeloma).
  • People who have a condition where myeloma cells are present in the blood (plasma cell leukemia).
  • People who have a condition called amyloidosis, where abnormal proteins build up in organs.
  • People who have a rare condition called POEMS syndrome, which affects multiple body systems including the nerves and organs.
  • People who have myeloma that has spread to the brain or spinal fluid, or who show signs of this.
  • People who have had a stem cell transplant within the 12 weeks before joining, or who are experiencing complications from a previous transplant where the donor cells are attacking the body.
  • People who currently have an active, uncontrolled infection caused by bacteria, fungi, or a virus.
  • People who have had another cancer within the past 3 years (with some exceptions, such as certain treated skin cancers or very early-stage cancers that have not spread).
  • People who have previously received a treatment that targets a protein called BCMA, or a treatment that redirects a type of immune cell called a T cell (CD3-redirecting therapy).
  • People who are unable to receive the treatment options offered by the trial doctors.
  • People who have received a live vaccine within 4 weeks before starting the trial.
  • People who have taken part in another clinical trial or received an experimental treatment within 30 days before starting this 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 7 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

Principal Investigator: Pfizer CT.gov Call Center, Pfizer

Phone: 1-800-718-1021

Australian sites

Blacktown Hospital, Blacktown, New South Wales
Concord Repatriation General Hospital, Concord, New South Wales
Sunshine Coast University Hospital, Birtinya, Queensland
Royal Brisbane and Women's Hospital, Brisbane, Queensland
St Vincent's Hospital (Melbourne), Fitzroy, Victoria
Barwon Health, Geelong, Victoria
Sir Charles Gairdner Hospital, Haematology Clinical Trials, Nedlands, Western Australia

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
8 February 2024
Est. completion
30 August 2026

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇧🇪 Belgium 🇧🇷 Brazil 🇨🇦 Canada 🇨🇱 Chile 🇭🇷 Croatia 🇨🇿 Czechia 🇩🇰 Denmark 🇫🇮 Finland 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece 🇮🇱 Israel 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇹 Portugal 🇸🇰 Slovakia 🇸🇮 Slovenia 🇰🇷 South Korea 🇪🇸 Spain 🇸🇪 Sweden 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Progression free survival per International Myeloma Working Group criteria

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: 7 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