Phase 1 Myeloma Trial, Recruiting NCT06768489 Sponsor: Janssen Research & Development, LLC Condition: Myeloma
Back to Myeloma

Phase 1 Myeloma Trial, Recruiting

NCT06768489
Recruiting Phase 1 🇦🇺 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 have been officially diagnosed with multiple myeloma based on standard diagnostic guidelines
  • Depending on which treatment group applies to you: you have had 1 to 3 previous treatments for multiple myeloma (including specific drug types called proteasome inhibitors and immunomodulatory drugs), OR you have never been treated for multiple myeloma before, OR you have had at least 1 or 2 prior treatments including specific drugs (confirm with trial site which group applies to you)
  • You weigh at least 40 kilograms (about 88 pounds)
  • You are able to carry out basic daily activities, either fully or with some limitations (this is measured on a standard scale called ECOG — confirm with trial site)
  • Your multiple myeloma can be measured through blood tests, urine tests, or certain types of scans at the time of screening

Who may not be able to join:

  • You have a serious active infection (such as a viral, bacterial, or fungal infection) that currently requires treatment
  • You have an autoimmune disease that required treatment with immune-suppressing medicines within the last 6 months
  • You have had a serious heart condition recently, such as a heart attack, unstable chest pain, or heart bypass surgery within the last 6 months, or you have moderate-to-severe heart failure
  • You have recently received certain cancer treatments, including targeted therapies, chemotherapy, antibody treatments, or radiation, within specific time periods before joining (confirm with trial site for exact timeframes)
  • You received a type of cell therapy called CAR-T or similar gene-modified cell therapy within the last 90 days
  • You had a donor stem cell transplant within the last 6 months, or your own stem cells were transplanted within the last 12 weeks
  • You still have side effects from previous cancer treatment that have not mostly cleared up (with some exceptions such as hair loss or mild nerve problems)
  • You have previously been treated with a type of therapy that redirects immune cells called T cells (CD3-redirecting therapy)
  • You need extra oxygen to breathe properly on an ongoing basis
  • You have HIV, active hepatitis B, or active hepatitis C
  • You have had a stroke or seizure within the last 6 months

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 26 July 2026
Phase 1: approximately ~10% 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: Janssen Research & Development, LLC Clinical Trial, Janssen Research & Development, LLC

Phone: 844-434-4210

Australian sites

Monash Medical Centre, Clayton,
St Vincents Hospital Melbourne, Fitzroy,
Peter MacCallum Cancer Centre, Melbourne,
Calvary Mater Newcastle Hospital, Waratah,
Wollongong Hospital, Wollongong,

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 1
Registry
ClinicalTrials.gov
Start date
4 December 2024
Est. completion
2 January 2029

Where this trial is recruiting

🇦🇺 Australia 🇮🇱 Israel 🇳🇱 Netherlands 🇪🇸 Spain

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

Primary endpoints

Part 1: Number of Participants with Dose-limiting Toxicity (DLT); Number of Participants with Adverse Events (AEs) by Severity; Number of Participants with Clinically Significant Laboratory Abnormalities

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: 26 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