Trials / Not Yet Recruiting
Not Yet RecruitingNCT07315373
Optimal Dose of Zanubrutinib to Treat Adult Immune Thrombocytopenia
The FIND Study: A Dose-finding Study to Identify the Optimal Dose of Zanubrutinib in Adults With Immune Thrombocytopenia
- Status
- Not Yet Recruiting
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Peking University People's Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this clinical trial is to find the best dose of zanubrutinib when used together with high-dose dexamethasone for adults who are newly diagnosed with primary immune thrombocytopenia (ITP), and to learn how safe and effective this combination treatment is.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Zanubrutinib 80mg/d | Zanubrutinib: 80 mg taken orally once daily for 26 weeks |
| DRUG | High dose dexamethasone | Dexamethasone: 40 mg taken orally once daily for 4 consecutive days at the beginning of treatment. A second identical 4-day course may be repeated after 2 weeks if an adequate initial platelet response is not achieved. |
| DRUG | Zanubrutinib 160mg/d | Zanubrutinib: 160 mg taken orally once daily for 26 weeks |
| DRUG | Zanubrutinib 240mg/d | Zanubrutinib: 240 mg taken orally once daily for 26 weeks |
Timeline
- Start date
- 2025-12-25
- Primary completion
- 2028-12-30
- Completion
- 2029-06-30
- First posted
- 2026-01-02
- Last updated
- 2026-01-02
Source: ClinicalTrials.gov record NCT07315373. Inclusion in this directory is not an endorsement.