TAVALISSE (fostamatinib disodium)
Tavalisse helps adult patients with chronic immune thrombocytopenia (ITP) who have not seen enough improvement from previous therapies. It specifically addresses low platelet counts by targeting the underlying biological processes that lead to their destruction. Doctors use this medication to manage the condition when other standard treatments have failed to provide an adequate response.
How TAVALISSE Works
This medication works by inhibiting spleen tyrosine kinase (SYK) through its primary metabolite, R406. By blocking signal transduction in B-cell and Fc-activating receptors, the drug reduces the antibody-mediated destruction of platelets.
Development Insights
Details
- Status
- Prescription
- First Approved
- 2018-04-17
- Patent Cliff
- 2032
- Routes
- ORAL
- Dosage Forms
- TABLET
TAVALISSE Approval History
What TAVALISSE Treats
2 indicationsTAVALISSE is approved for 2 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.
- Thrombocytopenia
- Immune Thrombocytopenia
TAVALISSE Competitive Set
ProThree rings of competition based on shared molecular targets and treated indications.
Indication competitors
Same indication, different mechanism — what else might this patient receive?
Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.
What's emerging in TAVALISSE's indications
See all emerging drugs →Phase 3 candidates targeting molecules with no FDA-approved drug, in indications TAVALISSE treats. First-in-class if their pivotal trials read out positive.
Drugs Similar to TAVALISSE
3 of 9FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.
Clinical Trial Registry
43 trials| Trial | Sponsor ID | Phase | Status | Title |
|---|---|---|---|---|
| NCT06948097 | 10002084 002084-H | Ph 1 | not yet recruiting | Syk Inhibition in MItigating Lung Allograft Rejection (SIMILAR): A Trial to Evaluate the Safety and Tolerability of Fostamatinib in Lung Transplant Patients With Donor-Specific Antibodies |
| NCT05904093 | 10001619 001619-H | Ph 1 | recruiting | Study to Evaluate the Safety and Tolerability of Escalating Doses of Fostamatinib in Subjects With Stable Sickle Cell Disease |
| NCT06564207 FOSTA-ARDS | INOVA-2023-169 | Ph 2 | not yet recruiting | Fostamatinib for Treating Acute Respiratory Distress Syndrome (ARDS) in Hospitalized Adults |
| NCT06233110 | Pro00113327 | Ph 1 | recruiting | Ruxolitinib Plus Fostamatinib for Steroid Refractory cGvHD |
| NCT05502783 results posted | 10000758 000758-H | Ph 2 | terminated | Using Fostamatinib to Treat Post-Hematopoietic Stem Cell Transplant Immune-mediated Cytopenias |
| NCT04581954 MATIS | 20HH5926 2020-001750-22 | Ph 1, Ph 2 | completed | Inflammatory Signal Inhibitors for COVID-19 (MATIS) |
| NCT05509582 | 10000760 000760-H | Ph 2 | withdrawn | Extension Study (Extended Access) of Syk-inhibition Using Fostamatinib to Treat Posttransplant Immune-mediated Cytopenias |
| NCT05593770 NECTAR results posted | ACTIV-4 | Ph 2, Ph 3 | terminated | International Sites: Novel Experimental COVID-19 Therapies Affecting Host Response |
| NCT05030675 | 2020-1117 NCI-2021-08494, 2020-1117 | Ph 1 | completed | Fostamatinib for the Treatment of Lower-risk Myelodysplastic Syndromes or Chronic Myelomonocytic Leukemia Who Have Failed Therapy With Hypomethylating Agents |
| NCT04924660 NECTAR results posted | 210982 | Ph 2, Ph 3 | completed | Novel Experimental COVID-19 Therapies Affecting Host Response |
| NCT03991780 FOSTAMR | 18HH4488 2018-000027-14 | Ph 1, Ph 2 | active not recruiting | Fostamatinib in the Treatment of Chronic Active Antibody Mediated Rejection |
| NCT04543279 results posted | 202011080 | Ph 2 | terminated | Fostamatinib as a Single Agent or in Combination With Ruxolitinib for Treatment of Patients With Myelofibrosis With Severe Thrombocytopenia |
| NCT02077192 results posted | C-935788-049 2013-005454-30 | Ph 3 | completed | Open Label Study of R788 in the Treatment of Persistent/Chronic Immune Thrombocytopenic Purpura (ITP) |
| NCT04629703 | C-935788-061 | Ph 3 | completed | Double-Blind, Randomized, Placebo-Controlled, Multi-Center Phase 3 Study to Evaluate the Efficacy and Safety of Fostamatinib in COVID-19 Subjects |
| NCT03764618 results posted | C-935788-057 | Ph 3 | completed | A Phase 3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Study of Fostamatinib Disodium in the Treatment of wAIHA |
| NCT02611063 | Pro00064227 | Ph 1 | completed | Evaluation of Fostamatinib in Patients With cGVHD After Allogeneic Stem Cell Transplant |
| NCT05040698 | JFR-001 | Ph 2 | completed | Study of the Effect of Fostamatinib Upon Cutaneous Inflammation in the Setting of Hidradenitis Suppurativa |
| NCT04138927 | C-935788-058 | Ph 3 | enrolling by invitation | A Phase 3 Open Label Extension Study of Fostamatinib Disodium in the Treatment of Warm Antibody Autoimmune Hemolytic Anemia |
| NCT04579393 results posted | 10000110 000110-H | Ph 2 | completed | Fostamatinib for Hospitalized Adults With COVID-19 |
| NCT02076399 FIT results posted | C-935788-047 2013-005452-15 | Ph 3 | completed | A Efficacy and Safety Study of R935788 in the Treatment of Persistent/Chronic Immune Thrombocytopenic Purpura (ITP) |
| NCT02076412 FIT results posted | C-935788-048 2013-005453-76 | Ph 3 | completed | A Efficacy and Safety Study of Fostamatinib in the Treatment of Persistent/Chronic Immune Thrombocytopenic Purpura (ITP) |
| NCT00798096 results posted | D4300C00024 C-935788-017 | Ph 2 | completed | Efficacy and Safety Study of Fostamatinib Disodium Tablets to Treat T-Cell Lymphoma |
| NCT00923481 results posted | 090138 09-C-0138 | Ph 2 | completed | A Broad Multi-histology Phase II Study of the Multi-Kinase Inhibitor R935788 (Fostamatinib Disodium) in Advanced Colorectal, Non-small Cell Lung, Head and Neck Hepatocellular and Renal Cell Carcinomas, and Pheochromocytoma and Thyroid Tumors (Multi-H... |
| NCT01499303 results posted | D4302C00001 | Ph 2 | completed | Study to Learn if 200mg Test Drug (Fostamatinib) Helps People With Large B-Cell Lymphoma,a Type of Blood Cancer |
| NCT02092961 OSKIRA 4 SS results posted | D4300C00004Sub | Ph 2 | terminated | Randomised Double-Blind, Placebo-Controlled, Parallel Group Study in Patients With Active Rheumatoid Arthritis:Magnetic Resonance Imaging Sub-Study |
| NCT01563978 Oskira ABPM results posted | D4300C00033 2011-006070-73 | Ph 2 | completed | Study of the Effect of Fostamatinib Twice Daily on Blood Pressure in Patients With Rheumatoid Arthritis |
| NCT01197534 OSKIRA - 2 results posted | D4300C00002 2010-020744-35 | Ph 3 | completed | Evaluation of Effectiveness of Two Dosing Regimens of Fostamatinib Compared to Placebo in Patients With Rheumatoid Arthritis (RA) Who Are Taking Disease Modifying Anti-rheumatic Drug (DMARD) But Not Responding. |
| NCT01197521 OSKIRA - 1 results posted | D4300C00001 2010-020743-12 | Ph 3 | completed | Evaluation of Effectiveness of Two Dosing Regimens of Fostamatinib Compared to Placebo in Patients With Rheumatoid Arthritis (RA) Who Are Taking Methotrexate But Not Responding. |
| NCT01197755 OSKIRA - 3 results posted | D4300C00003 2010-020745-27 | Ph 3 | completed | Evaluation of Effectiveness of Two Dosing Regimens of Fostamatinib Compared to Placebo in Patients With Rheumatoid Arthritis (RA) Who Are Taking Methotrexate and Have Had Inadequate Response to Single TNF-alpha Antagonist |
| NCT01569074 OSKIRA-Asia-1 results posted | D4300C00008 | Ph 2 | terminated | Evaluation of Safety and Effectiveness of Fostamatinib Compared to Placebo in Patients in Asia With Rheumatoid Arthritis |
| NCT01242514 OSKIRA-X results posted | D4300C00005 2010-020892-22 | Ph 3 | terminated | Evaluation of Long-term Safety and Effectiveness of Fostamatinib in the Treatment of Rheumatoid Arthritis (RA) |
| NCT01640054 OSKIRA-Asia-1X results posted | D4300C00029 | Ph 2 | terminated | A Long Term Study to Assess the Safety of Fostamatinib in Patients in Asia With Rheumatoid Arthritis |
| NCT01725230 Statin DDI | D4300C00039 | Ph 1 | completed | Assess the Pharmacokinetics of Rosuvastatin and Simvastatin When Administered Alone or in Combination With Fostamatinib |
| NCT01311622 | D4300C00013 | Ph 1 | completed | Effects of Administration of Fostamatinib on Blood Concentrations of Warfarin in Healthy Subjects |
| NCT01598571 | D4300C00027 QBR112696 | Ph 1 | completed | Study in Healthy Males to Assess Bioavailability of Single Fostamatinib With iv Micro Tracer Dose |
| NCT01276262 | D4300C00012 | Ph 1 | completed | Effects of Administration of Fostamatinib on Blood Concentrations of an Oral Contraceptive in Healthy Female Subjects |
| NCT01387308 | D4300C00018 | Ph 1 | completed | Study in Healthy Males to Assess the Bioavailability of 4 Different Fostamatinib Tablets |
| NCT01355354 | D4300C00026 | Ph 1 | completed | Effects of Administration of Fostamatinib on Blood Concentrations of Digoxin in Healthy Subjects |
| NCT01336218 | D4300C00015 | Ph 1 | completed | Effects of Administration of Fostamatinib on Blood Concentrations of Rifampicin in Healthy Subjects. |
| NCT01309854 | D4300C00014 | Ph 1 | completed | Effects of Administration of Fostamatinib on Blood Concentrations of Pioglitazone in Healthy Subjects |
| NCT01222455 | D4300C00010 | Ph 1 | completed | A Study of Fostamatinib in Subjects With Impaired Hepatic (Liver) Function |
| NCT01245790 | D4300C00009 | Ph 1 | completed | A Study of Fostamatinib in Subjects With Impaired Kidney Function |
| NCT01208155 | D4300C00016 | Ph 1 | completed | Study in Healthy Males to Assess Bioavailability of 4 Different Fostamatinib Tablets |
Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
TAVALISSE FDA Label Details
Indications & Usage
FDA Label (PDF)TAVALISSE is indicated for the treatment of Thrombocytopenia; Immune Thrombocytopenia.
TAVALISSE Patents & Exclusivity
Patents (14 active)
Pro Intelligence Preview
Deep insights for TAVALISSE
Revenue Insights
- • Quarterly revenue tracking
- • Historical trend analysis
Patent Timeline
- • Cliff: 2032
- • 56 active patents
Trial Analysis
- • 59 total trials
- • Stage: Declining
Competitive Landscape
- • 9 similar drugs
- • Same target/indication analysis
Full approval history • All patents • Revenue trends • Competitor analysis
Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.
How We Calculate These Metrics
Trial Activity Stage
Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.
Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.
- Growth: High proportion of early-phase trials (Phase 1/2), active development
- Expansion: Significant Phase 3 activity, approaching or pursuing approvals
- Mature: Substantial Phase 4 post-marketing studies
- Stable: Mixed phase distribution, steady development
- Declining: Low active trial ratio, reduced R&D investment