The Efficacy and Safety of Hydroxychloroquine Plus TPO-RA in Antinuclear Antibody-positive Patients With Primary Immune Thrombocytopenia-- The Multicenter, Randomized, Open-labled Clinical Trial

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn if hydroxychloroquine (HCQ) plus thrombopoietin receptor agonists (TPO-RA) works to treat primary immune thrombocytopenia with positive anti-nuclear antibodies in adults. It will also learn about the safety of HCQ plus TPO-RA. The main questions it aims to answer are: Does HCQ plus TPO-RA raise the response rate in participants, compared to TPO-RA alone? Does HCQ plus TPO-RA prolong the response duration in participants, compared to Pred alone? Does HCQ plus TPO-RA decrease the dose of TPO-RA to maintain response in participants, compared to TPO-RA alone? What medical problems do participants have when taking HCQ plus TPO-RA? Researchers will compare HCQ plus TPO-RA with TPO-RA alone to see if HCQ plus TPO-RA works better to treat primary immune thrombocytopenia with positive anti-nuclear antibodies. Participants will: Take TPO-RA every day for no more than 24 weeks, adjust the dose of TPO-RA according to the platelet level, with or without HCQ twice a day for 1 year; Visit the clinic once every 1 weeks for the first 8 weeks, and once every 2-4 weeks in the following 10 months for checkups and tests; Keep a diary of their symptoms

Eligibility
Participation Requirements
Sex: All
Minimum Age: 15
Maximum Age: 99
Healthy Volunteers: f
View:

• Age is above 15 years old.

• Before randomization, the clinical diagnosis is primary immune thrombocytopenia. The platelet count is less than 30×10\^9 / L within 1 week before enrollment, or platelet count is less than 50×10\^9 / L with bleeding symptoms within 1 week before enrollment.

• The antinuclear antibody is positive.

• Other autoantibodies (mainly including dsDNA antibodies, SSA, SSB, RNP, β 2-GP, ACA, ANCA) are negative.

• Participants who had received at least two HD-DXM 40 mg/d ×4 d, failed or relapsed, or received standard dose prednisone (1-2 mg/kg/d) for 4 weeks, the platelet count remained \<30×10 9 / L, or the platelet count normalized but decreased with prednisone tappering off, or prednisone 30mg to maintain the platelet number.

• Prothrombin time does not exceed ± 3s of the normal value ranget, activated partial thrombin time is not outside normal range ± 10s; no history of coagulopathy except ITP.

⁃ (6)Understand the study procedures and sign the written informed consent form.

Locations
Other Locations
China
Qingpu Branch of Zhongshan Hospital, Fudan University
RECRUITING
Shanghai
Shanghai Jinshan Hospital
RECRUITING
Shanghai
Shanghai Zhongshan Hospital
RECRUITING
Shanghai
Wusong Hospital, Zhongshan Hospital, Fudan University
RECRUITING
Shanghai
Hong Kong Special Administrative Region
Health and Humanity Research Centre, Hongkong, China.
RECRUITING
Hong Kong
Macao Special Administrative Region
Dr. Stanley Ho Medical Foundation
RECRUITING
Macao
University Hospital, Macau University of Science and Technology.
RECRUITING
Macao
Contact Information
Primary
Lili Ji
ji.lili@zs-hospital.sh.cn
86-021-64041990
Time Frame
Start Date: 2024-07
Estimated Completion Date: 2026-12
Participants
Target number of participants: 126
Treatments
Experimental: HCQ plus TPO-RA group
This group is experiment group. Participants will take eltrombopag for at least 24 weeks, the dose of eltrombopag is adjusted according to participants' platelet count, with HCQ twice a day for 1 year
Placebo_comparator: TPO-RA group
This group is control group. Participants will take eltrombopag for at least 24 weeks, the dose of eltrombopag is adjusted according to participants' platelet count.
Sponsors
Collaborators: Dr. Stanley Ho Medical Foundation, Macau, Macau University of Science and Technology Hospital, Health and Humanity Research Centre, Hongkong, Zhongshan Wusong Hospital, Fudan University, Shanghai Zhongshan Hospital, Shanghai Jinshan Hospital, Zhongshan Qingpu Hospital, Fudan University
Leads: Yunfeng Cheng

This content was sourced from clinicaltrials.gov