Myeloma Trial, Recruiting NCT06245629 Sponsor: Uppsala University Condition: Myeloma
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Myeloma Trial, Recruiting

NCT06245629
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:

  • You have been diagnosed with multiple myeloma that came back for the first time after having a stem cell transplant using your own stem cells (called an autologous stem cell transplant, or ASCT).
  • You received a second autologous stem cell transplant (using your own stem cells) as part of your treatment for this relapse, carried out at UUH (Uppsala University Hospital).
  • Your preparation treatment (conditioning) before that second transplant used either a combination of bortezomib, bendamustine, and melphalan, or high-dose melphalan on its own.

Who may not be able to join:

  • You received two stem cell transplants in a row (called a tandem transplant) as part of your first or second round of treatment.
  • You received a stem cell transplant using someone else's stem cells (called an allogeneic transplant) as part of your first or second round of treatment.
  • Your medical records do not contain enough information to meet the required data requirements — this includes having records of key dates (such as transplant dates and treatment start dates), hospital records from your second transplant, at least one follow-up appointment, and records of when your myeloma came back and what treatment followed (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 26 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: Honar Cherif, MD, PhD, Uppsala University

Phone: +4623492000

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
Sponsor
Uppsala University
Registry
ClinicalTrials.gov
Start date
24 November 2024
Est. completion
31 March 2025

Where this trial is recruiting

🇸🇪 Sweden

Primary endpoints

Mean difference in time to next treatment (TNT) after ASCT1 and ASCT2 for each individual patient

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