Active Ingredient History
TELAVANCIN (VIBATIV®) is a lipoglycopeptide antibacterial that is a synthetic derivative of vancomycin. It exerts concentration-dependent, bactericidal activity against Gram-positive organisms in vitro. TELAVANCIN (VIBATIV®) inhibits cell wall biosynthesis by binding to late-stage peptidoglycan precursors, including lipid II. It also binds to the bacterial membrane and disrupts membrane barrier function. TELAVANCIN (VIBATIV®) is indicated for the treatment of adult patients with complicated skin and skin structure infections caused by susceptible isolates of the following Gram-positive microorganisms: Staphylococcus aureus (including methicillin-susceptible and -resistant isolates), Streptococcus pyogenes, Streptococcus agalactiae, Streptococcus anginosus group (includes S. anginosus, S. intermedius, and S. constellatus), or Enterococcus faecalis (vancomycin-susceptible isolates only). It is also indicated for the treatment of adult patients with hospital-acquired and ventilator-associated bacterial pneumonia (HABP/VABP), caused by susceptible isolates of Staphylococcus aureus (both methicillin-susceptible and -resistant isolates). It should be reserved for use when alternative treatments are not suitable. NCATS
Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Abscess (Phase 2)
Bacteremia (Phase 3)
Burns (Phase 2)
Cellulitis (Phase 2)
Cystic Fibrosis (Phase 4)
Gram-Positive Bacterial Infections (Phase 4)
Healthy Volunteers (Phase 1)
Infections (Phase 2)
Kidney Diseases (Phase 1)
Kidney Failure, Chronic (Phase 4)
Pneumonia, Bacterial (Phase 3)
Staphylococcal Infections (Phase 3)
Ulcer (Phase 2)
Wound Infection (Phase 2)
Trial | Phase | Start Date | Organizations | Indications |
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