Ozmosi | ACT-462206 Drug Profile
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ACT-462206

Alternative Names: act-462206
Clinical Status: Inactive
Latest Update: 2021-10-26
Latest Update Note: PubMed Publication

Product Description

ACT-462206 is a new, potent, and selective dual orexin receptor antagonist (DORA) that inhibits the stimulating effects of the orexin peptides at both the orexin 1 and 2 receptors. It decreases wakefulness and increases non-rapid eye movement (non-REM) and REM sleep while maintaining natural sleep architectures in rat and dog electroencephalography/electromyography (EEG/EMG) experiments. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/25147058/)

Mechanisms of Action: OX1R Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Idorsia
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Healthy Volunteers

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT01954589

AC-074-101

P1

Completed

Healthy Volunteers

2012-01-01

2019-03-20