Last update 04 Apr 2026

EU-103

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
Anti-VSIG4 antibody – Eutilex, Anti-VSIG4 antibody(Eutilex), EU 103
+ [1]
Target
VSIG4
Action
inhibitors, stimulants
Mechanism
VSIG4 inhibitors(V-set and immunoglobulin domain-containing protein 4 inhibitors), Immunostimulants
Therapeutic Areas
Neoplasms
Active Indication-
Inactive Indication
Metastatic Solid TumorSolid tumor
Originator Organization
Eutilex Co., Ltd.Eutilex Co., Ltd.
Active Organization-
Inactive Organization
Eutilex Co., Ltd.Eutilex Co., Ltd.
License Organization-
Drug Highest PhasePendingPhase 1
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with EU-103
NCT05798026
/ Unknown statusPhase 1
A Dose-escalation, Single-arm, Open-Label, Phase 1 Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of EU103 in an Advanced or Metastatic Solid Tumors Who Have Failed Standard Therapy
100 Clinical Results associated with EU-103
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100 Translational Medicine associated with EU-103
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100 Patents (Medical) associated with EU-103
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100 Deals associated with EU-103
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Metastatic Solid TumorPhase 1
South Korea
Eutilex Co., Ltd.Eutilex Co., Ltd.
08 Aug 2023
Solid tumorPhase 1
South Korea
Eutilex Co., Ltd.Eutilex Co., Ltd.
08 Aug 2023
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Translational Medicine

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Deal

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Core Patent

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Clinical Trial

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Approval

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Biosimilar

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Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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