Suvratoxumab - Aridis Pharmaceuticals/Biosynexus/GlaxoSmithKline/Regeneron Pharmaceuticals
Alternative Names: AR-320; human IgG1 mAb; MEDI-4893; Suvratoxumab - AstraZenecaLatest Information Update: 30 Dec 2024
At a glance
- Originator Biosynexus; GlaxoSmithKline; Regeneron Pharmaceuticals
- Developer Aridis Pharmaceuticals; AstraZeneca
- Class Anti-infectives; Monoclonal antibodies
- Mechanism of Action Bacterial toxin modulators; Immunostimulants
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
- Available For Licensing Yes
Highest Development Phases
- Suspended Staphylococcal infections; Ventilator associated pneumonia
Most Recent Events
- 20 Dec 2024 Suvratoxumab is available for licensing as of 20 Dec 2024. https://www.aridispharma.com/
- 03 Nov 2023 Suspended - Phase-II for Ventilator-associated-pneumonia (Prevention) in USA, Czech Republic, Switzerland, United Kingdom, Hungary, Germany (IV)
- 03 Nov 2023 Suspended - Phase-III for Staphylococcal infections (Prevention) (IV)