PTCY Plus uhCG/EGF for Graft Versus Host Disease Prophylaxis

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-70
SponsorHenry Ford Health System

About this trial

So this a Phase I study with primary objective to determine the feasibility and safety of combining post-transplant cyclophosphamide and urinary-derived human chorionic gonadotropin and epidermal growth factor (uhCG/EGF) as graft versus host disease prophylaxis in stem cell transplant with MMUDs Secondary objectives are to determine the incidence acute and chronic GVHD, progression-free survival , and overall survival

Eligibility criteria

Qualifiers

Patients with hematologic malignancy who have the indication for Allogeneic SCT and have no MRD or MUD.

Age 18-70 years old

Performance score of at least 80% by Karnofsky

Creatinine clearance should be >60 ml/min

Disqualifiers

Positive for HIV, HBsAg, HCV or other viral hepatitis or cirrhosis from any cause

Active or prior CNS leukemia, unless in complete remission for at least 2 months.

History of serious chronic mental disorder or drug-abuse accompanied by documented problems of compliance with therapeutic programs.

Uncontrolled infection

Trial design

Treatments tested in this trial

  • uhCG/EGF

Treatment groups

18 Participants
are divided into 1 treatment group

Sponsors and collaborators