Efficacy and Safety of Cytotect®CP, Hyperimmune Anti-CMV IVIg as CMV Prophylaxis in Patients Developing Acute Grade II-IV GVHD After Allogeneic Hematopoietic Cell Transplantation.

PHASE2TerminatedINTERVENTIONAL
Enrollment

2

Participants

Timeline

Start Date

September 13, 2022

Primary Completion Date

August 24, 2023

Study Completion Date

August 24, 2023

Conditions
Cytomegalovirus Infections
Interventions
DRUG

Cytotect®CP

"Cytotect®CP in two phases:~Induction phase: 1 ml/kg/week for 4 weeks Maintenance phase: 1 ml/kg/2 weeks for 12 weeks or corticosteroid dose \< 0.5 mg/kg, according to which condition occurs first.~Patients developing CMV infection under Cytotect®CP must be given standard anti-CMV treatment (Gancyclovir or Foscarnet) according to their center procedure. Cytotect®CP will be maintained"

Trial Locations (1)

Unknown

Hop Claude Huriez Chu Lille, Lille

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Biotest

INDUSTRY

lead

University Hospital, Lille

OTHER

NCT05370976 - Efficacy and Safety of Cytotect®CP, Hyperimmune Anti-CMV IVIg as CMV Prophylaxis in Patients Developing Acute Grade II-IV GVHD After Allogeneic Hematopoietic Cell Transplantation. | Biotech Hunter | Biotech Hunter