Skip to content

Eltrombopag treatment for dose-reduction of corticosteroid in corticosteroid dependent adult chronic immune thrombocytopenia (ITP) patients.

Eltrombopag treatment for dose-reduction of corticosteroid in corticosteroid dependent adult chronic immune thrombocytopenia (ITP) patients. - Eltrombopag treatment for dose-reduction of corticosteroid in corticosteroid dependent adult chronic immune thrombocytopenia (ITP) patients.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011396
Enrollment
40
Registered
2013-08-10
Start date
2013-07-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corticosteroid Dependent Adult Chronic Immune Thrombocytopenia

Interventions

Eltrombopag 12.5mg to 50mg

Sponsors

Hematology/ Oncology, Iwate Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult (over than 20 years old) chronic ITP patients (<10x104/µl) under the treatment of corticosteroid 2. One of the followings A. Corticosteroid dependent (refractory) B. Strong request of patient for discontinuation of corticosteroid treatment C. Any medical reason for difficulty of continuation of corticosteroid treatment 3. Negative anti-phospholipid antibody 4. Obtainable written informed consent

Exclusion criteria

Exclusion criteria: 1. Any history of thrombo-embolic events. 2. Any hereditary disorder that may cause thrombo- embolic events such as ATIII deficiency or Protein C/S deficiency. 3. Any history of allergy/ intolerance to the study drug. 4. Pregnant, possibly pregnant and lactating women as well as women who intend to become pregnant within the proposed study period. 5. Any concomitant drugs or therapy that may influence the result of the study. 6. Renal or hepatic dysfunction/insufficiency. 7. HIV infection, HBV infection 7. Subjects judged as unsuitable for participation in the study for any reason by the physicians in charge of the study. 8. Unable to participate all sessions of the study.

Design outcomes

Primary

MeasureTime frame
Number of patients who can replace prednisolone with eltrombopag

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026