Overview
Teicoplanin is a glycopeptide antibiotic consisting of a mixture of several compounds, five major (named teicoplanin A2-1 through A2-5) and four minor (named teicoplanin RS-1 through RS-4). All teicoplanins share a same glycopeptide core, teicoplanin A3-1, but differ in the length and conformation of side chains attached to their β-D-glucosamine moiety.
Indication
For the treatment of bacterial infections caused by susceptible microorganisms.
Associated Conditions
- Angina Pectoris
- Anginal Pain
- Bacteremia
- Bloodstream Infections (BSI)
- Bone and Joint Infections
- Clostridium Difficile
- Clostridium Difficile Infection (CDI)
- Community Acquired Pneumonia (CAP)
- Complicated Urinary Tract Infection
- Infective Endocarditis (IE)
- Lower Respiratory Tract and Lung Infections
- Non-complicated Skin and Soft Tissue Infections
- Nosocomial Pneumonia
- Peritonitis
- Skin and Soft Tissue Infections (SSTIs)
- Urinary Tract Infection
Clinical Trials
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Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2012/05/04 | Phase 4 | UNKNOWN | Clinica Universidad de Navarra, Universidad de Navarra | ||
2009/06/19 | Phase 1 | Withdrawn | Aarhus University Hospital | ||
2008/07/21 | Phase 4 | Completed | University of Athens | ||
2007/04/19 | N/A | Completed | PETHEMA Foundation | ||
2007/03/30 | Phase 4 | Completed | |||
2007/02/02 | Phase 3 | Terminated | |||
2007/01/30 | Phase 2 | Completed | Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) | ||
2006/08/24 | Phase 4 | UNKNOWN |
FDA Drug Approvals
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Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| No FDA approvals found for this drug. | |||||
EMA Drug Approvals
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|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
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|---|---|---|---|---|---|
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NMPA Drug Approvals
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| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
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| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
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Health Canada Drug Approvals
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CIMA AEMPS Drug Approvals
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Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| TEICOPLANINA HIKMA 200 MG POLVO PARA SOLUCION INYECTABLE Y PARA PERFUSION EFG | 85875 | POLVO PARA SOLUCIÓN INYECTABLE Y PARA PERFUSIÓN | Uso Hospitalario | Commercialized | |
| TEICOPLANINA ACCORDPHARMA 400 MG POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE Y PARA PERFUSION EFG | 78342 | POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE | Uso Hospitalario | Not Commercialized | |
| TEICOPLANINA HIKMA 400 MG POLVO PARA SOLUCION INYECTABLE Y PARA PERFUSION EFG | 85874 | POLVO PARA SOLUCIÓN INYECTABLE Y PARA PERFUSIÓN | Uso Hospitalario | Commercialized | |
| TEICOPLANINA SALA 200 MG POLVO PARA SOLUCION INYECTABLE Y PARA PERFUSION EFG | Laboratorio Reig Jofre, S.A. | 78750 | POLVO PARA SOLUCIÓN INYECTABLE Y PARA PERFUSIÓN | Uso Hospitalario | Commercialized |
Philippines FDA Drug Approvals
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Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
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| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
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UK EMC Drug Information
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Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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| No UK EMC drug information found for this drug. | |||||
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