A Clinical Study on the Efficacy and Safety of Herombopag in the Treatment of Senile Primary ITP

Exclusion Criteria

• •Patients who did not respond to previous treatment with herombopag;
• •A history of allergy to thrombopoietin receptor agonist (TPO-RA) drugs;
• •Combined with other important organ dysfunction, such as liver and kidney failure, cardiac insufficiency, etc.
• •Secondary thrombocytopenia, such as rheumatic immune disease, chronic liver disease, hyperlienism, malignant hematologic disease, bone marrow hematopoietic exhaustion disease (such as AA, MDS), hereditary thrombocytopenia, CVID, drug-induced thrombocytopenia, etc.;
• •Receive TPO-RA medication within 2 weeks prior to treatment;
• •Non-steroidal anti-inflammatory drugs (aspirin, salicylate, etc.) and anticoagulants (warfarin, clopidogrel, etc.) should be taken during treatment, which have an impact on platelet function.
• •There are severe active bleeding symptoms, such as gastrointestinal bleeding, intracranial bleeding, etc.
• •Severe thrombotic disease, such as transient ischemic attack, myocardial infarction, pulmonary embolism, deep vein thrombosis, and disseminated intravascular coagulation (DIC), occurred within 6 months prior to the screening period;
• •Have a New York Heart Society (NYHA) Class 3 or 4 congestive heart failure, or have a history of NYHA Class 3/4 congestive heart failure with a left ejection fraction (LVEF) of \< 45% within 4 weeks prior to treatment;
• •Positive anti-human immunodeficiency virus antibody or anti-treponema pallidum specific antibody; Hepatitis virus positive, such as HBV, HCV, etc.
• •A history of cirrhosis;
• •Bone marrow reticulum fiber staining (MF) ≥2 grade;
• •Have an active infection that is difficult to control;
• •Have a history of or accompanied by malignant tumors;
• •Pregnant or lactating women;
• •Any other conditions that the investigator determines are not suitable for participation in the study.