TheraRadar
Data updated: May 26, 2026

TAVALISSE (fostamatinib disodium)

Trial Activity: Declining 6 active trials
First-in-Class Orphan Drug
Immunology Approved 2018-04-17

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.

Source: FDA Label • RIGEL PHARMS

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

AstraZeneca conducting 36 trials (61%)
55 indications explored (Broad Platform)
rheumatoid arthritis (22 trials)
healthy (7 trials)
pharmacokinetics (6 trials)
1
Indication
--
Phase 3 Trials
8
Years on Market

Details

Status
Prescription
First Approved
2018-04-17
Patent Cliff
2032

Pro Metrics

Patent cliff and revenue data

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Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: FOSTAMATINIB DISODIUM

TAVALISSE Approval History

2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
4 FDA actions from 2018 to 2025
Feb 2025 SUPPL
Label · Labeling
Apr 2018 ORIGINAL
New Drug · Type 1 - New Molecular Entity

What TAVALISSE Treats

2 indications

TAVALISSE 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
Source: FDA Label

TAVALISSE Competitive Set

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Three rings of competition based on shared molecular targets and treated indications.

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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

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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 9

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

ALVAIZ
ELTROMBOPAG CHOLINE
2 shared
Teva
Shared indications:
ThrombocytopeniaImmune Thrombocytopenia
DOPTELET
AVATROMBOPAG MALEATE
2 shared
AKARX INC
Shared indications:
ThrombocytopeniaImmune Thrombocytopenia
DOPTELET SPRINKLE
AVATROMBOPAG MALEATE
2 shared
AKARX INC
Shared indications:
ThrombocytopeniaImmune Thrombocytopenia
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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
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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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.

View full patent landscape →
14 OB patents · 4 families · 197 international docs across 48 countries

TAVALISSE Patents & Exclusivity

Latest Patent: Jul 2032

Patents (14 active)

US8951504 Expires Jul 27, 2032
US8771648 Expires Jul 27, 2032
US7449458 Expires Sep 4, 2031
US8263122 Expires Nov 24, 2030
US8652492 Expires Nov 6, 2028
US9283238 Expires Jun 17, 2026
US8912170 Expires Jun 17, 2026
US8163902 Expires Jun 17, 2026
US8445485 Expires Jun 17, 2026
US7989448 Expires Jun 12, 2026
US7538108 Expires Mar 28, 2026
US9266912 Expires Jan 19, 2026
US8211889 Expires Jan 19, 2026
USRE48898 Expires Jan 19, 2026
Source: FDA Orange Book

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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
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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