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Dalbavancin - Durata Therapeutics

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Drug Profile

Dalbavancin - Durata Therapeutics

Alternative Names: A-A-1; BI-397; Dalbavancin hydrochloride; Dalvance; MDL-63,397; V-Glycopeptide; VER 001; VGE; Xydalba; Zevan; Zeven

Latest Information Update: 22 Jan 2024

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At a glance

  • Originator Vicuron Pharmaceuticals
  • Developer Cipher Pharmaceuticals; Durata Therapeutics; Pfizer
  • Class Antibacterials; Glycopeptides; Peptide antibiotics
  • Mechanism of Action Cell wall inhibitors; Peptidoglycan inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Osteomyelitis
  • New Molecular Entity Yes
  • Available For Licensing Yes

Highest Development Phases

  • Marketed Skin and soft tissue infections
  • Phase II Bacterial endocarditis; Osteomyelitis
  • No development reported Bacterial infections; Catheter infections; Diabetic foot ulcer; Gonorrhoea; Pneumonia

Most Recent Events

  • 31 Dec 2023 Durata Therapeutics completes a phase III trial in Skin and soft tissue infections (In infants, In adolescents, In children) in US, Bulgaria, Chile, Guatemala, Panama, Ukraine, Mexico, Colombia, Georgia, Greece, Latvia, Lithuania and Spain.(IV) (NCT02814916)
  • 19 Jan 2022 Launched for Skin and soft tissue infections in Canada (IV)
  • 23 Jul 2021 Launched for Skin and soft tissue infections (In adolescents, In children, In infants, In neonates) in USA (IV)

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