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Lemborexant

Alternative Names: lemborexant, e2006, dayvigo
Latest Update: 2024-11-27
Latest Update Note: Clinical Trial Update

Product Description

Lemborexant is a medication used in the management and treatment of insomnia. It is in the dual orexin antagonist class of medications. This activity outlines the indications, actions, and contraindications for lemborexant as a valuable agent in managing insomnia. (Sourced from: https://www.ncbi.nlm.nih.gov/books/NBK559070/)

Mechanisms of Action: OX1R Antagonist,OX2R Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Approved

Approved Countries: Australia | Canada | Hong Kong | India | Indonesia | Israel | Japan | Malaysia | Mexico | Philippines | Singapore | Taiwan | United Arab Emirates | United States

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 Lemborexant

Countries in Clinic: Canada, China, Korea, Taiwan, United States, Unknown Location

Active Clinical Trial Count: 6

Highest Development Phases

Phase 3: Insomnia

Phase 2: Delirium

Phase 1: Chronic Obstructive Pulmonary Disease|Sleep Apnea, Obstructive

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

PROTEX

P2

Not yet recruiting

Delirium

2027-01-30

E2006-J082-204

P2

Completed

Insomnia

2024-04-26

E2006-J086-311

P3

Completed

Insomnia

2023-03-17

90%

E2006-A001-113

P1

Completed

Chronic Obstructive Pulmonary Disease|Sleep Apnea, Obstructive

2022-02-10

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