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Eritoran

Alternative Names: eritoran, e5564, e-5564
Latest Update: 2024-07-12
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: TLR4 Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Eisai
Company Location: BUNKYO-KU TOKOYO 112 M0
Company CEO: Haruo Naito
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Eritoran

Countries in Clinic: Australia, Belgium, Canada, Colombia, Croatia, Czech Republic, Estonia, Finland, France, Germany, Hungary, India, Ireland, Israel, Italy, Japan, Nepal, Netherlands, New Zealand, Pakistan, Portugal, Romania, Saudi Arabia, Serbia, Slovenia, Spain, Switzerland, United Kingdom, United States

Active Clinical Trial Count: 1

Highest Development Phases

Phase 3: COVID-19|Influenza, Human|Pneumonia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

REMAP-CAP

P3

Recruiting

Pneumonia|COVID-19|Influenza, Human

2026-02-01

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