Clinical trial · Interventional
Clinical Study of rhTPO in Hematopoietic Stem Cell Mobilization for Autologous Transplantation in Acute Leukemia
Recombinant Human Thrombopoietin for Autologous Hematopoietic Stem Cell Mobilization in Acute Leukemia: A Single-Arm Prospective Study
NCT06955858CI-TRIAL-00089258not yet recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hematopoietic Stem Cell Mobilization | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Recombinant Human Thrombopoietin(rhTPO) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- The group of rhTPO
- interventionNames
- Drug: Recombinant Human Thrombopoietin(rhTPO)
Primary outcomes (1)
- measure
- total CD34+ cell count
- timeFrame
- two weeks
- description
- Median total number of CD34+ cells collected
Secondary outcomes (5)
- measure
- the proportion of patients collecting more than or equal to 2*10^6 CD34+ cells/kg
- timeFrame
- two weeks
- measure
- the proportion of patients collecting more than or equal to 5*10^6 CD34+ cells/kg
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age 18~65 years, regardless of gender. 2. Histopathologically confirmed acute leukemia with immunohistochemical validation 3. Sustained complete hematologic remission with documented minimal residual disease (MRD) negativity. 4. Eastern Cooperative Oncology Group (ECOG) performance status smaller than 2 and a life expectancy of more than 6 months 5. No active infectious disease; no severe organ failure. 6. Willingness to participate with written informed consent for study enrollment. Exclusion Criteria: 1. Liver dysfunction (alanine aminotransferase or bilirubin greater than two times the normal upper limit). 2. Renal dysfunction (creatinine or urea higher than 1.5 times the normal upper limit). 3. 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 4. rhTPO aller- gies. 5. Severe prior thrombosis-event. 6. History of other malignancy, unless cured for more than 3 years 7. Pregnant or lactating women 8. Severe infectious disease (uncured tuberculosis, pulmonary aspergillosis) 9. Epilepsia, dementia or any mental disease requiring treatment. 10. Other conditions deemed inappropriate for study participation by the investigator.
References
Publications (0)
Data not yet available
No reference posted for this study.