A Safety and Efficacy Study of R935788 in the Treatment of Warm Antibody Autoimmune Hemolytic Anemia (AIHA)
Part of paid clinical trials in Gilbert, Arizona.
- Sponsor
- Rigel Pharmaceuticals
- Study ID
- NCT02612558
- Phase
- PHASE2
- Status
- Completed
Conditions
- Warm Antibody Autoimmune Hemolytic Anemia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Fostamatinib 150 mg bid — DRUGFostamatinib 150 mg bid. The dose of Fostamatinib may be reduced at any time to as low as 100 mg PO once daily (qd) if dose limiting adverse events are observed.
Study Details
The purpose of this study is to evaluate whether fostamatinib is safe and effective in the treatment of Warm Antibody Autoimmune Hemolytic Anemia (AIHA).
Key Dates
- Start date
- Jul 31, 2016
- Status verified
- Jul 2021
- Primary completion
- Dec 31, 2019
- Completion
- Dec 31, 2019
Study Design
- Enrollment
- 26 participants (actual)
- Allocation
- NA
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Fostamatinib 150 mgFostamatinib 150 mg bid (morning and evening) over the course of 24 weeks
Primary Outcome Measure
Hemoglobin response [ Time Frame: by Week 24 ]
Locations (31)
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