A Trial to Evaluate the Safety and Preliminary Efficacy of iMesenchymal Stromal Cells(iMSC) in Subjects With SR-aGVHD

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age4-70
SponsorAnhui Provincial Hospital

About this trial

A study to evaluate the safety and preliminary efficacy of iMSC in subjects with SR-aGVHD

Eligibility criteria

Qualifiers

None

Disqualifiers

Accepted systemic or local treatment of mesenchymal stem cells;

Have severe allergy to blood products or have allergy history of heterologous protein;

Expected survival period within 3 months;

Alanine transaminase(ALT)or Aspartate aminotransferase(AST)>2*upper limit of normal(ULN);Creatinine clearance rate≤30ml/min or Blood Urea Nitrogen(BUN)>2*upper limit of normal(ULN), International Normalized Ratio (INR)>1.5*upper limit of normal(ULN);

Trial design

Treatments tested in this trial

  • iMSC

Treatment groups

12 Participants
are divided into 1 treatment group

Sponsors and collaborators

Anhui Provincial Hospital

Lead sponsor

Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences (IHCAMS)

Collaborator