Rituximab for Serious Aplastic Anemia With Platelet Transfusion Refractoriness

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-70
SponsorInstitute of Hematology & Blood Diseases Hospital, China

About this trial

Due to long-term dependence on platelet transfusion, some severe aplastic anemia (SAA) patients suffer platelet transfusion refractoriness (PTR). Unlike immune thrombocytopenia (ITP), glucocorticoids and human immunoglobulin (IVIg) are generally ineffective for PTR. Due to the lack of effective intervention methods, patients with PTR suffer increased platelet transfusions, bleeding events and treatment costs, prolonged hospital stays, and decreased survival rate. SAA with PTR has become a challenge for physicians. The experiment aims to explore the efficacy of rituximab in the treatment of SAA with PTR, and establish a new effective, safe treatment method with relatively low treatment cost.

Eligibility criteria

Qualifiers

Initial diagnosed SAA with PTR

Age>18 years old, regardless of gender

Initial diagnosed SAA with PTR

Age>18 years old, regardless of gender

Disqualifiers

Allergy to rituximab

Severe active infection

Hypogammaglobulinemia

Pregnant and lactating women

Trial design

Treatments tested in this trial

  • Rituximab

Treatment groups

20 Participants
are divided into 1 treatment group