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

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

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

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Healthy Volunteers: f
View:

• Patients voluntarily participated in the study and signed informed consent;

• Age ≥60 years old, gender unlimited;

• ECOG PS ≤2;

• Expected survival ≥6 months;

• A definitive diagnosis of ITP, including newly diagnosed, chronic, and persistent ITP;

• PLT \< 30×109/L for at least two consecutive times with an interval of at least 1 day before medication

• Patients with laboratory test results meet the following criteria: a. alanine aminotransferase (ALT) 3.0 x or less normal limit (ULN), aspartate aminotransferase (AST) 3.0 x ULN or less; b. Serum total bilirubin ≤1.5×ULN; c. Serum creatinine ≤1.5×ULN;

• The researchers determined that patients could be treated with hexapopal.

Locations
Other Locations
China
Chinese academy of medical science and blood disease hospital
RECRUITING
Tianjin
Contact Information
Primary
Yunfei Chen
chenyunfei@ihcams.ac.cn
+8618502220788
Time Frame
Start Date: 2025-03-03
Estimated Completion Date: 2027-12
Participants
Target number of participants: 80
Treatments
Experimental: Herombopag
Herombopag 2.5mg per tablet
Sponsors
Leads: Institute of Hematology & Blood Diseases Hospital, China

This content was sourced from clinicaltrials.gov