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Dovitinib

Alternative Names: dovitinib, chir-258, tki258, tk1258, tk-1258, tk 1258
Latest Update: 2024-11-12
Latest Update Note: News Article

Product Description

Dovitinib is a pan-tyrosine kinase inhibitor targeting fibroblast growth factor receptor (FGFR), vascular endothelial growth factor receptor (VEGFR) and other receptor tyrosine kinases (RTKs). Allarity exclusively in-licensed it (globally) from Novartis, who had completed a Phase 3 study in renal cell carcinoma (RCC) in addition to several promising Phase 2 studies in breast, liver and endometrial cancer and GIST. (Sourced from: https://allarity.com/pipeline/dovitinib/)

Mechanisms of Action: RTK Inhibitor,FGFR Inhibitor,VEGF Inhibitor,KITl Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Novartis
Company Location: BASEL V8 CH 4056
Company CEO: Vasant Narasimhan
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Dovitinib

Countries in Clinic: United States

Active Clinical Trial Count: 1

Highest Development Phases

Phase 1: Diarrhea|Neutropenia|Thrombocytopenia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

AL-2003

P1

Recruiting

Thrombocytopenia|Diarrhea|Neutropenia

2024-10-01

21%

AL-2003

P1

Recruiting

Thrombocytopenia|Diarrhea|Neutropenia

2024-10-01

21%

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