Approved & therapeutic
Daptomycin
Cubicin
Daptomycin is a cyclic lipopeptide antibiotic active against Gram-positive organisms including methicillin-resistant Staphylococcus aureus, approved for complicated skin and skin structure infections and for S. aureus bloodstream infections including right-sided endocarditis.
Also known as: Cubicin RF, LY146032
- Status
- Daptomycin is approved by the U.S. FDA and has official prescribing information.
- Evidence
- Approved labeling. Official prescribing information exists, based on clinical trials in people.
- Half-life
- Approximately 8 to 9 hours in patients with normal renal function, supporting once-daily dosing.
- How it's taken
- Intravenous infusion or injection
- Mechanism
- Immune modulation
How Daptomycin works
Daptomycin inserts its lipid tail into the Gram-positive cytoplasmic membrane in a calcium-dependent manner, oligomerises, and causes rapid membrane depolarisation through potassium efflux. Cell death follows without cell lysis. Because the target is the membrane rather than a protein or the ribosome, it retains activity against organisms resistant to most other classes.
What research has looked at
- Rapidly bactericidal against Gram-positive pathogens including MRSA and vancomycin-resistant enterococci.
- Once-daily intravenous dosing.
- A distinct mechanism from beta-lactams and glycopeptides, so cross-resistance is uncommon.
Evidence level: Approved labeling. Official prescribing information exists, based on clinical trials in people. These are areas studied or reported, not promised effects.
Reported side effects and risks
- Daptomycin is inactivated by pulmonary surfactant and is therefore ineffective in pneumonia. This is a mechanistic failure, not a spectrum gap, and is one of the more consequential facts about the drug.
- Skeletal muscle toxicity: creatine kinase elevation and, less often, rhabdomyolysis. Weekly CK monitoring is recommended, and concomitant statins are often held.
- Eosinophilic pneumonia has been reported, typically after two or more weeks of therapy, and requires immediate discontinuation.
- Peripheral neuropathy has been reported.
- It can cause a falsely prolonged prothrombin time and elevated INR depending on the reagent used.
Sources
- FDA approved-drug listing for daptomycin · U.S. Food & Drug Administration
- DailyMed prescribing information for daptomycin · NIH · DailyMed
- PubMed research on daptomycin surfactant inactivation pneumonia · NIH · National Library of Medicine
- DrugBank record for daptomycin · DrugBank
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Related compounds
Daptomycin FAQ
What is Daptomycin?
Daptomycin is a cyclic lipopeptide antibiotic active against Gram-positive organisms including methicillin-resistant Staphylococcus aureus, approved for complicated skin and skin structure infections and for S. aureus bloodstream infections including right-sided endocarditis.
How does Daptomycin work?
Daptomycin inserts its lipid tail into the Gram-positive cytoplasmic membrane in a calcium-dependent manner, oligomerises, and causes rapid membrane depolarisation through potassium efflux. Cell death follows without cell lysis. Because the target is the membrane rather than a protein or the ribosome, it retains activity against organisms resistant to most other classes.
Is Daptomycin FDA approved?
Yes. Daptomycin is approved by the U.S. FDA and has official prescribing information. Evidence level: approved labeling. Official prescribing information exists, based on clinical trials in people.
What is the half-life of Daptomycin?
Reported half-life: Approximately 8 to 9 hours in patients with normal renal function, supporting once-daily dosing.
How is Daptomycin taken?
Intravenous infusion or injection.
What side effects have been reported with Daptomycin?
Reported in the sources: Daptomycin is inactivated by pulmonary surfactant and is therefore ineffective in pneumonia. This is a mechanistic failure, not a spectrum gap, and is one of the more consequential facts about the drug; Skeletal muscle toxicity: creatine kinase elevation and, less often, rhabdomyolysis. Weekly CK monitoring is recommended, and concomitant statins are often held; Eosinophilic pneumonia has been reported, typically after two or more weeks of therapy, and requires immediate discontinuation; Peripheral neuropathy has been reported; It can cause a falsely prolonged prothrombin time and elevated INR depending on the reagent used.
Educational summary compiled from the sources listed above. Not medical advice. Peptide Vault does not sell, source or recommend any compound. Talk to a qualified clinician before starting or changing anything.