Myeloma Trial, Recruiting NCT06477783 Sponsor: Universitaire Ziekenhuizen KU Leuven Condition: Myeloma
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Myeloma Trial, Recruiting

NCT06477783
Recruiting Not Applicable

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 aged 18 years or older
  • People who are willing and able to provide written consent to participate
  • People who have been diagnosed with multiple myeloma that has come back (relapsed) and is no longer responding to treatment (refractory)
  • People who have already received at least three previous treatments for their multiple myeloma
  • People whose disease has stopped responding to at least one treatment from each of these three groups: a type of drug called a proteasome inhibitor, a type of drug called an immunomodulatory agent, and a drug that targets a protein called CD38 (an anti-CD38 monoclonal antibody)
  • People whose disease has been confirmed to be getting worse during or after their most recent treatment, based on established multiple myeloma response guidelines
  • People who are expected to begin treatment with a drug called teclistamab as part of their regular medical care, or who have already started teclistamab no more than 14 days before the planned screening visit

Who may not be able to join:

  • People who have previously taken part in a clinical trial involving teclistamab, whether in the treatment group or a comparison group, or who have received teclistamab through a special individual access program (Single Patient Request)
  • People who started teclistamab treatment more than 14 days before the planned screening visit

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 15 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Michel Delforge, MD, PhD, UZ Leuven Gasthuisberg

Phone: +32 16 34 68 80

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
1 December 2024
Est. completion
1 September 2027

Where this trial is recruiting

🇧🇪 Belgium

Primary endpoints

Overall response rate

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: 15 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