Feasibility Trial of Extracorporeal Iron Purification in Patients With Myelodysplastic Syndrome or Myelofibrosis

NARecruitingINTERVENTIONAL
Enrollment

13

Participants

Timeline

Start Date

September 26, 2025

Primary Completion Date

July 31, 2026

Study Completion Date

October 30, 2026

Conditions
Myelodysplastic SyndromeMyelofibrosis
Interventions
DEVICE

Low-volume continuous veno-venous haemodialysis with MEX-CD1 use

MEX-CD1 is a hyper-chelating colloidal solution that can be added to the dialysate to be used in low-volume continuous veno-venous hemodialysis. Intervention includes 3 low-volume continuous veno-venous hemodialysis for a duration of 4 hours each. For non-hospitalized patients, the treatment is performed on an outpatient basis.

Trial Locations (2)

69495

RECRUITING

Hôpital Lyon Sud, Oullins-Pierre-Bénite

RECRUITING

Hôpital Lyon Sud, Oullins-Pierre-Bénite

All Listed Sponsors
collaborator

MEXBrain 13 avenue Albert Einstein 69100 Villeurbanne

UNKNOWN

lead

Hospices Civils de Lyon

OTHER

NCT06781099 - Feasibility Trial of Extracorporeal Iron Purification in Patients With Myelodysplastic Syndrome or Myelofibrosis | Biotech Hunter | Biotech Hunter