The purpose of this study is to determine whether Recombinant Human Interleukin-11 (rhIL-11) Combination Low-dose Rituximab prednisone are effective and safe in the management of Steroid-Resistant/Relapsed Immune Thrombocytopenia (ITP).
Study Type
OBSERVATIONAL
Recombinant Human Interleukin-11 (rhIL-11) Combinating Low-dose Rituximab
Qilu Hospital, Shandong University
Jinan, Shandong, China
Evaluation of platelet response (Complete Response)
CR. A complete response (CR) was defined as a sustained (≥ 4 months) platelet count ≥ 100×109/L without recurrence of thrombocytopenia
Time frame: The time frame is up to 14 days per subject
Evaluation of platelet response (R)
R. A response (R) was defined as a sustained (≥ 4 months) platelet count ≥ 30×109/L without recurrence of thrombocytopenia
Time frame: The time frame is up to 14 days per subject
The time of rhIL-11 onset.
The time to platelet recovery (defined as the number of days from the start of the study to the first day with a platelet count of ≥30 × 109/L)
Time frame: The time frame is up to 28 days per subject.
DFS
The median disease-free survival periods
Time frame: The time frame is up to 90 days per subject.
The number and frequency of IL-11 associated adverse events.
Time frame: up to 14 days per subject
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