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Eltrombopag

Alternative Names: eltrombopag, revolade, promacta, sb497115, sb-497115-gr, ALVAIZ
Latest Update: 2025-04-18
Latest Update Note: Clinical Trial Update

Product Description

Eltrombopag, an orally administered, small-molecule non-peptide thrombopoietin receptor agonist, selectively binds to the transmembrane domain of the thrombopoietin receptor on the surface of platelets, megakaryocytes and megakaryocyte precursor cells. The drug acts via the Janus Kinase/Signal Transducer and Activator of Transcription (JAK/STAT) pathway to activate megakaryocyte proliferation and differentiation in bone marrow progenitor cells, similar to those observed with endogenous thrombopoietin.  (Sourced from: https://pubmed.ncbi.nlm.nih.gov/19368418/)

Mechanisms of Action: TPO Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Approved

Approved Countries: Algeria | Argentina | Australia | Austria | Bangladesh | Belgium | Bosnia | Brazil | Canada | Chile | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Ecuador | Egypt | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hong Kong | Hungary | Iceland | India | Indonesia | Ireland | Israel | Italy | Japan | Jordan | Korea | Latvia | Lebanon | Lithuania | Luxembourg | Malaysia | Morocco | Netherlands | New Zealand | Norway | Pakistan | Peru | Philippines | Poland | Portugal | Romania | Russia | Saudi Arabia | Serbia | Singapore | Slovakia | Slovenia | South Africa | Spain | Sri Lanka | Sweden | Switzerland | Taiwan | Thailand | Tunisia | Turkey | Ukraine | United Arab Emirates | United Kingdom | United States | Uruguay | Venezuela | Vietnam

Approved Indications: None

Known Adverse Events: None

Company: GSK
Company Location: BRENTFORD MIDDLESEX X0 TW8 9GS
Company CEO: Emma Walmsley
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Eltrombopag

Countries in Clinic: Bangladesh, China, Czech Republic, France, Germany, Japan, Switzerland, Taiwan

Active Clinical Trial Count: 14

Highest Development Phases

Phase 2: Acute Myeloid Leukemia|Anemia, Aplastic|Anemia, Refractory|Graft vs Host Disease|Lymphoma|Myelodysplastic Syndrome|Preleukemia|Purpura, Thrombocytopenic, Idiopathic|Stem Cell Transplant|Thrombocytopenia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2023-505788-35-00

P2

Unknown Status

Purpura, Thrombocytopenic, Idiopathic|Thrombocytopenia

2028-01-13

2015-003166-91

P2

Unknown status

Anemia, Refractory|Anemia, Aplastic

2025-11-22

EIT

P2

Recruiting

Thrombocytopenia|Purpura, Thrombocytopenic, Idiopathic

2025-08-31

CETB115L11201

P2

Active, not recruiting

Myelodysplastic Syndrome|Preleukemia

2025-04-24

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