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NCT05675319CompletedPhase 3

Allogeneic stem cell transplantation vs. conventional therapy as salvage therapy for relapsed / progressed patients with multiple myeloma after first-line therapy (AlloRelapseMMStudy)

Allogeneic stem cell transplantation vs. conventional therapy as salvage therapy for relapsed / progressive patients with multiple myeloma after a first-line therapy

Source: EU CTIS (euclinicaltrials.eu) · Last updated 5 Feb 2025

Brief summary (registry, in English)

The present clinical study aims to demonstrate the superiority of allogeneic stem (alloSCT) cell transplantation compared to conventional therapy for the difference in overall survival (OS) at 5 years in patients with multiple myeloma who have relapsed or progressed after first-line autologous hematopoietic stem cell therapy.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
400 (actual)
First submitted
16 Aug 2024
Start date
3 Mar 2023
Lead sponsor
University Medical Center Hamburg-Eppendorf
NCT number
NCT05675319
EU CT number
2024-510590-14-00
EudraCT number
2021-001005-67

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 400
  • 30 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior treatment with allogeneic stem cells
  • Participation in a clinical trial or taking an IMP within 30 days or five times the half-life of the IMP, whichever is longer, prior to study inclusion/enrollment

Other illness

  • Active hepatitis B or C infection or uncontrolled HIV infection
  • Other, active malignant disease
  • Progressive disease (PD) on salvage therapy

Lab values

  • Non-sufficient organ function defined as:  Bilirubin (in the absence of Meulengracht's disease), SGPT or SGOT ≥ 3 times higher than normal values  Cardiac ejection fraction ≤ 50 %  GFR < 30 ml/min  DLCO < 35 % or continuous oxygen dependency
  • Positive serum pregnancy test at screening and before first treatment or breastfeeding

Other

  • Patients are not included in the study if any one of criteria 1-6 are met and if criterion 7 is met before randomization:

Who the study is looking for

  • Patients eligible for study inclusion/enrollment must meet criteria 1-7 and all of the criteria (1-9) before randomization
  • CR/ PR or SD according to IMWG criteria after 3 cycles salvage therapy within the study
  • Multiple Myeloma
  • Age 18 - 65 years
  • A signed informed consent form must be obtained before participation in the study
  • Age 66 - 70 years, if comorbidity index according to Sorror score = 0 and ECOG ≤ 1
  • 1st relapse/ progression according to IMWG criteria after first-line therapy (consisting of induction therapy followed by autologous transplantation once or twice and maintenance therapy) Additionally: meeting the need for treatment based on the SLiM-CRAB-criteria
  • Negative pregnancy test in female patients
  • Maximum of 1 cycle salvage therapy prior to study inclusion/enrollment
  • Availability of a fully compatible stem cell donor (HLA-ident. sibling or 10/10 MUD or 9/10 MMUD if mismatch affects DQB) after 3 cycles salvage therapy

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (30)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitaetsklinikum Aachen AöR
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AachenGermanyCompleted
Universitaetsklinikum Augsburg
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AugsburgGermanyCompleted
HELIOS Klinikum Berlin Buch GmbH
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BerlinGermanyCompleted
Charite Universitaetsmedizin Berlin KöR
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BerlinGermanyCompleted
Universitaetsklinikum Bonn AöR
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BonnGermanyCompleted
Klinikum Chemnitz gGmbH
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ChemnitzGermanyCompleted
Universitaetsklinikum Carl Gustav Carus Dresden an der Technischen Universitaet Dresden AöR
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DresdenGermanyCompleted
Universitätsklinikum Düsseldorf
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DüsseldorfGermanyCompleted
Universitaetsklinikum Essen (AoR)
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EssenGermanyCompleted
Universitaetsklinikum Frankfurt AöR
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Frankfurt Am MainGermanyCompleted
Medical Center- University of Freiburg
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Freiburg im BreisgauGermanyCompleted
Universitaetsmedizin Goettingen
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GoettingenGermanyCompleted
Universitaetsklinikum Halle (Saale) AöR
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Halle SaaleGermanyCompleted
Asklepios Klinik St George
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HamburgGermanyCompleted
University Medical Center Hamburg-Eppendorf
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HamburgGermanyCompleted
Universitaetsklinikum Heidelberg AöR
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HeidelbergGermanyCompleted
Universitaetsklinikum Jena KöR
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JenaGermanyCompleted
Universitaetsklinikum Schleswig-Holstein AöR
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KielGermanyCompleted
Universitaetsmedizin der Johannes Gutenberg-Universitaet Mainz KöR
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MainzGermanyCompleted
Universitaetsklinikum Giessen und Marburg GmbH
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MarburgGermanyCompleted
Universitaetsklinikum Muenster AöR
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MuensterGermanyCompleted
Klinikum der Universitaet Muenchen AöR
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MunichGermanyCompleted
Klinikum rechts der Isar der TU Muenchen AöR
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MunichGermanyCompleted
Klinikum Nuernberg
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NurembergGermanyCompleted
Klinikum Oldenburg Aor
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OldenburgGermanyCompleted
Universitaetsklinikum Regensburg AöR
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RegensburgGermanyCompleted
Robert Bosch Krankenhaus GmbH
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StuttgartGermanyCompleted
Universitaetsklinikum Tuebingen AöR
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TuebingenGermanyCompleted
Universitaetsklinikum Ulm AoR
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UlmGermanyCompleted
Universitaetsklinikum Wuerzburg AöR
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WuerzburgGermanyCompleted

This page is information, not medical advice. Discuss any trial with your doctor.