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Danirixin

Alternative Names: danirixin, gsk1325756, gsk-1325756h, gsk 1325756h, gsk1325756h
Latest Update: 2024-04-01
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: CXCR2 Antagonist

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: GlaxoSmithKline
Company Location: BRENTFORD MIDDLESEX X0 TW8 9GS
Company CEO: Emma Walmsley
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Danirixin

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Chronic Obstructive Pulmonary Disease|Influenza, Human

Phase 1: Inflammation|Chronic Obstructive Pulmonary Disease|Respiratory Tract Infections|Bile Reflux|Respiratory Syncytial Virus Infections

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

GSK1325756, Phase 2, hospitalised Influenza Patients, RD, NAI co-administration, IV, PKPD

P2

Completed

Influenza, Human

2019-11-16

NCT03170232

P2

Terminated

Chronic Obstructive Pulmonary Disease

2018-11-15

NCT03250689

P2

Terminated

Chronic Obstructive Pulmonary Disease

2018-10-08

PH 2a,danirixin vs PBO BD 14days,randomised DB study evaluating the effect on NETs in lungs of COPD

P2

Completed

Chronic Obstructive Pulmonary Disease

2018-10-08

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