Clinical Study of rhTPO in Hematopoietic Stem Cell Mobilization for Autologous Transplantation in Acute Leukemia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorInstitute of Hematology & Blood Diseases Hospital, China

About this trial

Evaluation of the efficacy and safety of recombinant human thrombopoietin (rhTPO) at 300 U/kg/day for hematopoietic stem cell mobilization in autologous transplantation among acute leukemia patients

Eligibility criteria

Qualifiers

Age 18~65 years, regardless of gender.

Histopathologically confirmed acute leukemia with immunohistochemical validation

Sustained complete hematologic remission with documented minimal residual disease (MRD) negativity.

Eastern Cooperative Oncology Group (ECOG) performance status smaller than 2 and a life expectancy of more than 6 months

Disqualifiers

Liver dysfunction (alanine aminotransferase or bilirubin greater than two times the normal upper limit).

Renal dysfunction (creatinine or urea higher than 1.5 times the normal upper limit).

Any disease that could put patients at high risk, including but not limited to unstable cardiac disease, uncontrolled atrial fibrillation or hypertension, severe diabetic retinopathy

rhTPO aller- gies.

Trial design

Treatments tested in this trial

  • Recombinant Human Thrombopoietin(rhTPO)

Treatment groups

60 Participants
are divided into 1 treatment group