Építés alatt – nem éles oldal
Belépés
LeállítvaNo phase

Micro-transplantation in Elderly Patients With Acute Myeloid Leukemia

Megadott ok: Inclusion is proceeding too slowly

Key facts

Where
Clermont-Ferrand, Grenoble, Lille, Lyon, Nancy, Paris és Saint-Etienne, FranciaországSee the 7 sites

Where in Franciaország

  • CHU EstaingClermont-Ferrand, FranciaországNo longer taking part
  • Centre Hospitalier Universitaire de GrenobleGrenoble, FranciaországNo longer taking part
  • CHRU de LilleLille, FranciaországNo longer taking part
  • Centre Hospitalier Lyon SudLyon, FranciaországNo longer taking part
  • Centre Hospitalier Universitaire De NancyNancy, FranciaországNo longer taking part
  • Hôpital de la Pitié-SalpêtrièreParis, FranciaországNo longer taking part
  • Chu de Saint EtienneSaint-Etienne, FranciaországNo longer taking part

Trial details

Who runs it
Centre Hospitalier Universitaire de Saint Etienne
Trial code
NCT03439371
Record updated
2026. október 13.
Original description
This study aims at evaluating the safety and the tolerance of the micro-transplantation in elderly patients with acute myeloid leukemia who are ineligible to conventional allogeneic transplantation.Read full original descriptionShow less

A Phase II, Multicenter, Open Label Study Evaluating the Efficacy and the Tolerance of Micro-transplantation in Elderly Patients With Acute Myeloid Leukemia (MTSA)

This study aims at evaluating the safety and the tolerance of the micro-transplantation in elderly patients with acute myeloid leukemia who are ineligible to conventional allogeneic transplantation.

Inclusion: Patient affiliated to a social security regimen or beneficiary of the same; Signed written informed consent form; Patient, ≥ 60 years-old - < 75 years-old, with established diagnosis of de novo or secondary AML with intermediate-risk or adverse-risk cytogenetic profile, or with established myelodysplasic syndromes (RAEB), in pathologically confirmed complete remission following anti-leukemic induction therapy (<5% blasts); Contra-indication to conditioning regimen in conventional allogeneic transplantation.

Exclusion: Patient under guardianship or deprived of his liberty or any condition that may affect the patient's ability to understand and sign the informed consent; Patient with established diagnosis of acute myeloid leukemia with standard-risk cytogenetic profile; Promyelocytic leukemia t(15;17); CBF-AML t(8;21) or inv(16); Normal karyotype with a favorable molecular profile: NPM1+ and FLT3-; NPM1+, FLT3- and double mutation CEBPα or chronic myeloid leukemia in blastic phase; Refusing participation.

ClinicalTrials.gov NCT03439371