Phase 2 Myeloma Trial, Recruiting NCT04973605 Sponsor: BeOne Medicines Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT04973605
Recruiting Phase 2 🇦🇺 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 generally able to carry out basic daily activities, even if you need some help at times (this is measured on a standard scale called ECOG, scores 0–2).
  • You have been officially diagnosed with multiple myeloma, confirmed by a protein marker found in your blood and/or urine.
  • Your myeloma shows measurable levels of disease activity through specific blood or urine tests (confirm exact thresholds with trial site).
  • Your myeloma has come back or continued to grow after previous treatment, or has stopped responding to your most recent treatment.
  • Depending on which part of the trial you may join, you may need to have had at least 1, or at least 3, previous treatments — including certain types of drugs such as a proteasome inhibitor, an IMiD, and/or an anti-CD38 antibody drug (confirm which group applies to you with the trial site).
  • A specific genetic change in your myeloma cells, called a t(11;14) translocation, must be confirmed through a specialist lab test done on a fresh bone marrow sample taken at the start of the trial.
  • Your blood counts and organ function (including red blood cells, platelets, white blood cells, and liver function) must be at acceptable levels within 7 days before starting treatment.

Who may not be able to join:

  • You have a form of myeloma that does not produce detectable protein markers in the blood (called non-secretory myeloma).
  • You have a single isolated tumour made of myeloma cells (called solitary plasmacytoma).
  • You have an active condition where myeloma cells are circulating in large numbers in your blood (called plasma cell leukemia).
  • You have a related blood condition called Waldenström macroglobulinemia.
  • You have a condition called amyloidosis, where abnormal proteins build up in organs.
  • You have a rare condition called POEMS syndrome, which affects multiple parts of the body.
  • You have a long-term breathing condition that requires you to use oxygen continuously.
  • You have had a heart attack within the last 6 months, or have certain other significant heart problems such as severe heart failure, uncontrolled irregular heartbeat, or very poor heart pumping function (confirm details with trial site).
  • You have uncontrolled high blood pressure at the time of screening.
  • You have previously been treated with a drug called sonrotoclax or other drugs that work in a similar way (such as venetoclax).
  • You are known to have HIV.
  • You have an active hepatitis B or hepatitis C infection (though people with certain inactive forms of these infections may still be eligible — confirm with trial site).

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 21 July 2026
Phase 2: approximately ~30% 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: 1.877.828.5568

Australian sites

Canberra Hospital, Garran, Australian Capital Territory
Nepean Hospital, Kingswood, New South Wales
Monash Health, Clayton, Victoria
St Vincents Hospital Melbourne, Fitzroy, Victoria
The Alfred Hospital, Melbourne, Victoria
Royal Perth Hospital, Perth, 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 2
Sponsor
BeOne Medicines
Registry
ClinicalTrials.gov
Start date
16 September 2021
Est. completion
1 November 2026

Where this trial is recruiting

🇦🇺 Australia 🇧🇷 Brazil 🇨🇦 Canada 🇨🇳 China 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece 🇮🇹 Italy 🇸🇬 Singapore 🇰🇷 South Korea 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Part 1: Number Of Participants Experiencing Dose-limiting Toxicities (DLTs); Part 1 And 2: Number of Participants Reporting One or More Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs), Adverse Events Leading to Discontinuation and Adverse Events of Special Interest (AESIs).; Part 2: Overall response rate (ORR) as Assessed by Investigator; Part 2: Very Good Partial Response (VGPR) or Better Response Rate as Assessed by Investigator; Part 2: Complete Response (CR) or Stringent Complete Response (sCR) as Assessed by Investigator

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: 21 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