Phase 3 Myeloma Trial, Recruiting NCT07555938 Sponsor: Hoffmann-La Roche Condition: Myeloma
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Phase 3 Myeloma Trial, Recruiting

NCT07555938
Recruiting Phase 3

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 in good physical health and able to carry out daily activities, or your physical limitations are only due to pain or other local symptoms from your myeloma (confirm with trial site)
  • You have been diagnosed with multiple myeloma according to recognised international guidelines
  • You have already received between one and three rounds of treatment for your myeloma, which must have included at least two cycles of either a treatment targeting a protein called CD38, or a drug called lenalidomide
  • Your myeloma must be detectable through specific tests at the time of screening

Who may not be able to join:

  • You have a history of a condition called amyloidosis, which involves abnormal protein build-up in tissues (confirm with trial site)
  • You have a form of myeloma where large numbers of abnormal plasma cells are found in the blood (known as plasma cell leukemia), or your blood contains too many of these cells
  • You have a stomach or bowel condition that could affect how your body absorbs oral (swallowed) medicines
  • You have an active condition affecting the brain or nervous system, or a type of myeloma that does not produce measurable proteins in the blood or urine (known as non-secretory myeloma)

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 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: Clinical Trials, Hoffmann-La Roche

Phone: 888-662-6728

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
Registry
ClinicalTrials.gov
Start date
23 June 2026
Est. completion
31 October 2028

Where this trial is recruiting

🇯🇵 Japan Puerto Rico 🇰🇷 South Korea 🇺🇸 United States

Primary endpoints

Minimal Residual Disease (MRD)-Negative Complete Response (CR) Rate; Progression-Free Survival (PFS)

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