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Vancomycin 1.1%
Vancomycin inhibits cell wall synthesis in Gram-positive bacteria by binding to the D-alanyl-D-alanine terminus of cell wall precursors.
Vancomycin inhibits cell wall synthesis in Gram-positive bacteria by binding to the D-alanyl-D-alanine terminus of cell wall precursors. Used for Treatment of serious or severe bacterial infections caused by susceptible strains of methicillin-susceptible Staphylococcus aureus (MSSA), methicillin-resistant Staphylococcus aureus (MRSA), and other susceptible Gram-positive bacteria..
At a glance
| Generic name | Vancomycin 1.1% |
|---|---|
| Sponsor | Kurobe LLC |
| Drug class | glycopeptide antibiotic |
| Target | D-alanyl-D-alanine terminus of cell wall precursors |
| Modality | Small molecule |
| Therapeutic area | Infectious Disease |
| Phase | Phase 3 |
Mechanism of action
This prevents the incorporation of these precursors into the bacterial cell wall, ultimately leading to cell lysis and death. Vancomycin has a high affinity for the bacterial cell wall and is able to inhibit cell wall synthesis even at low concentrations.
Approved indications
- Treatment of serious or severe bacterial infections caused by susceptible strains of methicillin-susceptible Staphylococcus aureus (MSSA), methicillin-resistant Staphylococcus aureus (MRSA), and other susceptible Gram-positive bacteria.
Common side effects
- Nausea
- Vomiting
- Abdominal pain
- Diarrhea
- Anemia
- Thrombocytopenia
- Renal impairment
- Hypokalemia
- Hypomagnesemia
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Vancomycin 1.1% CI brief — competitive landscape report
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- Kurobe LLC portfolio CI