Clinical Trials in Japan / NCT06757257
Recruiting
Observational
Special Drug Use-results Survey for Long-term Use (Fostamatinib)
NCT06757257 · tracked via the Priya Life Science Japan tracker
Condition(s) studied
Chronic Idiopathic Thrombocytopenic Purpura
Study summary
The purpose of this survey is evaluating the safety and efficacy of long-term administration of fostamatinib for Japanese patients with chronic idiopathic thrombocytopenic purpura under actual conditions of use.
Eligibility
Inclusion Criteria:
* Patients with chronic idiopathic thrombocytopenic purpura who are treatment with fostamatinib for the first time.
Primary outcome measure(s)
- Adverse events — 18 months
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Research site | Tokyo and Japanese Other Cities | Japan | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06757257 on ClinicalTrials.gov ↗ ← All trials in Japan