Phase 2 Myeloma Trial, Recruiting
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.
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
Where this trial is recruiting
Primary endpoints
Current GVHD-free, relapse-free survival (cGRFS)
Can't join this trial?
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.