Master Framework For Relapse or Refractory Acute Myeloid Leukemia

NCT06459024 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 4000

Last updated 2026-03-10

No results posted yet for this study

Summary

This is an observational (non-interventional), prospective, cohort study that will collects data from patients diagnosed with relapsed or refractory acute myeloid leukemia afferent to the participanting clinical sites

Conditions

  • Acute Myeloid Leukemia, in Relapse
  • Acute Myeloid Leukemia Refractory

Interventions

OTHER

Registration into the STREAM platform

All patients fulfilling eligibility criteria will be registered into the STREAM platform. Baseline and follow up information will be recorded for each patient enrolled. Each patient will be followed up according to normal clinical practice up to 4 years.

Sponsors & Collaborators

  • Hospital Vall d'Hebron

    collaborator OTHER
  • Cyprus Institute of Neurology and Genetics

    collaborator OTHER
  • European LeukemiaNet

    collaborator NETWORK
  • Fundacion Para La Investigacion Hospital La Fe

    collaborator OTHER
  • Ostedusche Hematology and Oncology Study Group

    collaborator UNKNOWN
  • Ospedale Pediatrico Bambin Gesù

    collaborator OTHER
  • Czech Lymphoma Study Group

    collaborator OTHER
  • Charite University, Berlin, Germany

    collaborator OTHER
  • Fundación Instituto de Estudios de Ciencias de la Salud de Castilla y León

    collaborator OTHER
  • University of Bologna

    collaborator OTHER
  • Hannover Medical School

    collaborator OTHER
  • German Society for Pediatric Oncology and Hematology GPOH gGmbH

    collaborator OTHER
  • Toscana Life Sciences Sviluppo s.r.l.

    collaborator INDUSTRY
  • Lithuanian University of Health Sciences

    collaborator OTHER
  • Gruppo Italiano Malattie EMatologiche dell'Adulto

    collaborator OTHER
  • Time.Lex

    collaborator UNKNOWN
  • Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS

    lead OTHER

Principal Investigators

  • Giovanni Martinelli, MD, Prof · University of Bologna

Eligibility

Min Age
6 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-28
Primary Completion
2032-07-31
Completion
2032-07-31

Countries

  • Germany
  • Italy
  • Lithuania
  • Poland
  • Romania
  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06459024 on ClinicalTrials.gov