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Palmidrol

Alternative Names: palmidrol, palmitoylethanolamide, guanfacine extended release
Latest Update: 2024-12-09
Latest Update Note: Clinical Trial Update

Product Description

Palmitoyl ethanolamide is an N-(long-chain-acyl)ethanolamine that is the ethanolamide of palmitic (hexadecanoic) acid. It has a role as an anti-inflammatory drug, an antihypertensive agent, a neuroprotective agent and an anticonvulsant. It is a N-(long-chain-acyl)ethanolamine, an endocannabinoid and a N-(saturated fatty acyl)ethanolamine. It derives from a hexadecanoic acid.

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: Australia | Chile | India

Approved Indications: None

Known Adverse Events: None

Company: RDC Global
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Palmidrol

Countries in Clinic: Australia

Active Clinical Trial Count: 4

Highest Development Phases

Phase 3: Dermatitis, Atopic|Migraine Disorders|Rhinitis, Allergic

Phase 2: Healthy Volunteers

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

LEVESS

P2

Not yet recruiting

Healthy Volunteers

2027-01-01

MIGLEV-21

P3

Completed

Migraine Disorders

2023-03-09

95%

PEA-XMA-20

P3

Completed

Dermatitis, Atopic

2022-06-03

86%

ACTRN12619001368123

P3

Completed

Rhinitis, Allergic

2022-01-12

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