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AZD-5213

Alternative Names: azd-5213, azd5213, azd 5213
Latest Update: 2017-02-07
Latest Update Note: Clinical Trial Update

Product Description

AZD5213 is potent, competitive, rapidly reversible, functional antagonist (inverse agonist) at the human H3 receptor. (Sourced from: https://openinnovation.astrazeneca.com/clinical-research/clinical-molecules/azd5213.html)

Mechanisms of Action: H3 Inverse Agonist

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: AstraZeneca
Company Location: CAMBRIDGE X0 CB2 0AA
Company CEO: Pascal Soriot
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for AZD-5213

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Alzheimer Disease|Cognitive Dysfunction|Tourette Syndrome|Rett Syndrome|Low Back Pain

Phase 1: Healthy Volunteers

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

D3031C00001

P2

Completed

Low Back Pain

2015-05-01

D3032C00001

P2

Completed

Rett Syndrome|Tourette Syndrome

2015-02-01

D3030C00005

P2

Completed

Alzheimer Disease|Cognitive Dysfunction

2013-01-01

D3030C00004

P1

Completed

Healthy Volunteers

2011-10-01

Recent News Events

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