Phase 2 Myeloma Trial, Recruiting NCT03852407 Sponsor: University of Liege Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT03852407
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:

About the patient's diagnosis:

  • People diagnosed with one of the following blood cancers (confirmed by tissue testing): Acute Myeloid Leukaemia (AML) that is in remission or not rapidly worsening; Myelodysplastic Syndrome (MDS); Chronic Myeloid Leukaemia (CML) in a stable or early advanced phase; a group of bone marrow disorders called Myeloproliferative Diseases (MPD) that have not reached a severe stage; an overlap condition called MDS/MPD; Acute Lymphoblastic Leukaemia (ALL) in remission; Multiple Myeloma; Chronic Lymphocytic Leukaemia (CLL); Non-Hodgkin's Lymphoma (aggressive types must be responding to chemotherapy); or Hodgkin's Disease that is responding to chemotherapy or checkpoint inhibitor treatment

About the patient's situation:

  • People who would normally be considered for a standard bone marrow transplant from a donor, but for whom that approach is not possible due to being over 50 years old, having organ health concerns, or a decision made by the patient or their doctor
  • People with a lower-risk blood cancer for whom a less intensive transplant preparation approach is considered more appropriate (such as CLL or Mantle Cell Lymphoma)

Other patient criteria:

  • People aged 18 to 75 years old (children are not eligible for this trial)
  • People who are able to use reliable contraception during and for 12 months after treatment, if they are able to have children
  • People who have given their informed consent to participate (or whose legal guardian has done so where applicable)

About the stem cell donor:

  • The donor can be male or female, of any age
  • The donor must be either a brother or sister who is a full tissue-type (HLA) match, or an unrelated donor who matches on all 10 relevant tissue-type markers
  • The donor must weigh more than 15 kg
  • The donor must meet standard medical requirements for donating blood stem cells through a procedure called leukapheresis
  • The donor must have given informed consent to donate (or their legal guardian has done so where applicable)

Who may not be able to join:

Patients:

  • People who are HIV positive
  • People who have had a non-blood cancer (other than common skin cancers) that was active within the 3 years before transplant
  • People whose life expectancy is severely limited by a condition other than their blood cancer
  • People whose cancer has spread to the central nervous system and has not responded to treatment delivered directly into the spinal fluid
  • People with severe heart problems, including significant coronary artery disease, a heart pumping function below 40%, uncontrolled irregular heartbeat, or uncontrolled high blood pressure
  • People with severe lung problems, including a lung carbon monoxide transfer capacity below 40%, a need for continuous supplementary oxygen, or a key breathing measurement (FEV1) below 40%
  • People with severe liver conditions, including liver failure, cirrhosis with complications, alcoholic hepatitis, bleeding from oesophageal veins, liver-related brain problems, certain chronic viral liver infections with high bilirubin levels, or blocked bile ducts, among other serious liver conditions (confirm with trial site for full details)
  • People with an infection that is not currently under control
  • People whose general health and ability to perform daily activities falls below a set threshold on a standard medical scoring scale (Karnofsky score below 70%)
  • People who are pregnant or breastfeeding
  • People who are able to have children but are unwilling to use contraception during and for 12 months after treatment
  • People for whom the conditioning medications used in this trial (melphalan or Thymoglobulin) cannot be safely used

Donors:

  • Donors who are unable to undergo the stem cell collection procedure (leukapheresis) due to poor vein access or other reasons
  • Donors who do not meet the inclusion criteria listed above

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 21 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: Frédéric Baron, MD,Ph, Centre Hospitalier Universitaire de Liege

Phone: +32 4 366 72 01

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
Sponsor
University of Liege
Registry
ClinicalTrials.gov
Start date
4 February 2019
Est. completion
1 November 2033

Where this trial is recruiting

🇧🇪 Belgium

Primary endpoints

Current GVHD-free, relapse-free survival (cGRFS)

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: 21 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