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

ConditionHerombopag
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age60+
SponsorInstitute of Hematology & Blood Diseases Hospital, China

About this trial

The objective of this study was to evaluate the efficacy and safety of Herombopag in the treatment of elderly patients with ITP.

Eligibility criteria

Qualifiers

Patients voluntarily participated in the study and signed informed consent;

Age ≥60 years old, gender unlimited;

ECOG PS ≤2;

Expected survival ≥6 months;

Disqualifiers

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.;

Trial design

Treatments tested in this trial

  • herombopag olamine tablets

Treatment groups

80 Participants
are divided into 1 treatment group