Phase 2 Myeloma Trial, Recruiting NCT04935684 Sponsor: University Hospital, Clermont-Ferrand Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT04935684
Recruiting Phase 2

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 18 years old or older
  • You are a man or a woman
  • You are covered by a social security or health insurance system
  • You are having a specific type of stem cell transplant (using stem cells from the blood, not from umbilical cord blood) from a donor, for a blood cancer that is currently under control
  • You have read, understood, and signed a consent form agreeing to take part

Who may not be able to join:

  • Your blood cancer is currently getting worse or spreading at the time of the transplant
  • You have difficulty understanding the study, for example due to a language barrier or cognitive difficulties
  • You have a history of another active cancer, or had one in the last 3 years (a common type of skin cancer called basal cell carcinoma is not counted)
  • You have another serious illness that is not well controlled, such as severe heart, kidney, liver, or breathing problems, or a severe infection
  • You have problems controlling your bowel movements (fecal incontinence)
  • You are already taking part in another clinical trial that involves the transplant process, the drugs used to prevent rejection, treatment or prevention of a transplant complication called GvHD, or another trial testing a gut bacteria transplant (FMT) (confirm with trial site)
  • You are pregnant
  • You are under legal guardianship or a court-ordered protection arrangement

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 27 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

Principal Investigator: Jacques-Olivier BAY, MD, PhD, University Hospital, Clermont-Ferrand

Phone: +33473754963

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
Registry
ClinicalTrials.gov
Start date
20 December 2022
Est. completion
1 May 2030

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Graft-versus-host disease and Relapse-Free Survival (GRFS) rate after allogeneic hematopoietic stem cell transplantation

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: 27 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