rhTPO + CsA vs CsA in the Treatment of LR-MDS With Thrombocytopenia

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorPeking Union Medical College Hospital

About this trial

This study aims to compare the efficacy and safety of recombinant human thrombopoietin (rhTPO) + cyclosporine (CsA) and CsA monotherapy in the treatment of lower-risk myelodysplastic neoplasms with thrombocytopenia.

Eligibility criteria

Qualifiers

Age ≥ 18 years old;

Confirmed diagnosis of lower-risk MDS;

Platelet ≤ 30×109/L, or < 50×109/L and accompanied by bleeding events;

Baseline liver and kidney functions <2 ULN;

Disqualifiers

History of leukemia or stem cell transplantation, treatment-related MDS or malignant tumors;

With splenomegaly or myelofibrosis;

Infections or bleeding that cannot be controlled by standard treatment;

Any concurrent malignant tumors within the past 5 years, or basal cell carcinoma of the skin at the local site;

Trial design

Treatments tested in this trial

  • rhTPO
  • Cyclosporine (CsA)

Treatment groups

78 Participants
are divided into 2 treatment groups

Locations

This trial has no locations