Open Label Study of R788 in the Treatment of Persistent/Chronic Immune Thrombocytopenic Purpura (ITP)

Part of paid clinical trials in Tucson, Arizona.

Sponsor
Rigel Pharmaceuticals
Study ID
NCT02077192
Phase
PHASE3
Status
Completed

Conditions

  • Immune Thrombocytopenic Purpura

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

Study Details

The primary objective of this study was to assess the long term safety of fostamatinib in subjects with persistent/chronic ITP

Key Dates

Start date
Oct 31, 2014
Status verified
Dec 2023
Primary completion
Jun 2, 2020
Completion
Jun 2, 2020

Study Design

Enrollment
123 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Fostamatinib Disodium
    Fostamatinib Disodium tablet 100 mg or 150 mg by mouth twice a day

Primary Outcome Measure

Percentage of Subjects Who Achieved Platelet Count of at Least 50,000/µL Within 12 Weeks of Beginning Treatment up to 12 Months (Fostamatinib in 047/048 or 049):Version 1 [ Time Frame: Up to 12 months ]

Locations (9)

FacilityCityStateZIPSite coordinators
Arizona Oncology AssociatesTucsonArizona85710-
Bleeding & Clotting Disorders InstitutePeoriaIllinois61615-
Horizon Oncology Research, IncLafayetteIndiana47905-
Center for Cancer and Blood DisordersBethesdaMaryland20817-
Weill Cornell Medical College/New York Presbyterian HospitalNew YorkNew York10065-
Weill Cornell MedicineNew YorkNew York10065-
East Carolina University, Brody School of MedicineGreenvilleNorth Carolina27834-
W.G. "Bill" Hefner VA Medical CenterSalisburyNorth Carolina28144-
Signal Point Clinical Research Center LLCMiddletownOhio45042-

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