A Phase II Multicenter Single-armed Study Using Subject-specific Minimal Residual Disease Markers to Adopt Treatment After Allogeneic Stem Cell Transplantation for Subjects With Myelodysplastic Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The goal of this interventional study is to evaluate if pre-emptive intervention using Azacitidine and / or donor lymphocytes or tapering of immune suppression in measurable residual disease (MRD) positive subjects can prevent clinical relapse. Participants will undergo MRD surveillance and be subjected to intervention in case of MRD positivity. Results will be compared with NMDSG14B, part one, in which MRD was analyzed in included patients without recieving intervention.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Signed informed consent

• Age ≥ 18 years

• Subjects eligible for SCT

• Subjects having the disease MDS, mixed myelodysplastic/myeloproliferative syndrome or AML with myelodysplasia related dysplasia and 20-29% marrow blasts

• All female subjects of childbearing potential have to have negative pregnancy test within 2 weeks prior to inclusion to the study

Locations
Other Locations
Sweden
Department of Hematology, Karolinska University Hospital
RECRUITING
Stockholm
Contact Information
Primary
Magnus Tobiasson, PhD
magnus.tobiasson@ki.se
0046858580000
Time Frame
Start Date: 2022-11-22
Estimated Completion Date: 2026-12
Participants
Target number of participants: 200
Treatments
Experimental: Intervention in MRD positive patients
Azacitidine and / or Donor lymphocytes or tapering of immune suppression
Sponsors
Collaborators: Nordic MDS Group
Leads: Karolinska University Hospital

This content was sourced from clinicaltrials.gov