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Evidence: HighPeptideFDA ApprovedLipoglycopeptideFDA-approved 2014 · DalvanceHalf-life ~8.5 days

Dalbavancin

A skin-infection antibiotic that can be a single infusion

Dalbavancin is a lipoglycopeptide antibiotic: a natural glycopeptide modified with a fatty tail that anchors it in membranes and plasma proteins. Its effective half-life of about 8.5 days means a course of treatment can be one infusion, or two a week apart.

Overview

What is it?

Glycopeptide antibiotics such as vancomycin kill Gram-positive bacteria by binding the building blocks of their cell wall. Dalbavancin adds a lipid side chain, which anchors it in the bacterial membrane and binds it to plasma proteins, giving an effective half-life of about 8.5 days. The practical consequence is a course that takes one or two visits rather than a week or more of daily infusions.

The DISCOVER 1 and DISCOVER 2 trials pooled 1,312 patients with skin infections: early clinical response was 79.7% on dalbavancin and 79.8% on vancomycin followed by linezolid. Among patients with Staphylococcus aureus, including MRSA, clinical success was 90.6% and 93.8%.

Its label warns of hypersensitivity, infusion-related reactions, liver effects and Clostridioides difficile diarrhoea. A pooled safety analysis found lower rates of kidney toxicity than with at least 10 days of intravenous vancomycin (3.7% against 9.3%).

Children are covered by the approval. In the paediatric study, dosing was by age and weight, with clinical response assessed from 48 hours to 54 days after treatment, and audiology and bowel flora checked in a subset.

Structured data

At a Glance

Every value in this table is printed from the Grey Peptides dataset, the same record the compound explorer and comparison tool read, so the three can never disagree.

ClassA semi-synthetic lipoglycopeptide antibiotic, a modified natural glycopeptide with a fatty side chain, that binds the building blocks of the bacterial cell wall; approved in the US in 2014 as Dalvance for acute bacterial skin and skin structure infections, given as one or two intravenous doses.
Half-lifeeffective half-life about 8.5 days (204 hours); terminal half-life about 346 hours
Label dose1,500 or 1,000 then 500 mg (a single 1,500 mg dose, or 1,000 mg followed one week later by 500 mg; lower doses if creatinine clearance is under 30 mL/min and not on dialysis, intravenous infusion over 30 minutes)
US statusFDA Approved
Evidence levelHigh
Last reviewed2026-10-03

Educational information, not medical advice. The doses on this page come from approved labels, published studies and, where no study exists, amounts reported by users. None is a recommendation for you. An unapproved compound has no established safe or effective human dose, and products sold for “research use only” are not made or tested for people. Talk to a doctor before acting on anything on this site, including before you start, stop or change any medicine or dose. Full medical disclaimer.

Interactive

Half-Life: How Much Remains

The dataset records a half-life of effective half-life about 8.5 days (204 hours); terminal half-life about 346 hours for Dalbavancin. After each half-life, half of what was in the circulation is gone, so about 3% remains after five. Real clearance varies with the person, the dose, the route and kidney or liver function; this is arithmetic on a published figure, not a dosing tool.

Time since a single dose
Evidence

Published Research

The studies behind dalbavancin, from their PubMed abstracts.

Human2014

DISCOVER 1 and 2: once-weekly against daily therapy

In the pooled analysis of 1,312 patients with skin infections, early clinical response was 79.7% on dalbavancin and 79.8% on vancomycin-linezolid, meeting noninferiority; with S. aureus, including MRSA, success was 90.6% against 93.8%.

PMID: 24897082
Human2025

DOTS: Staphylococcus aureus in the bloodstream

In 200 participants, the probability of a more desirable day-70 outcome with dalbavancin against standard therapy was 47.7%; clinical efficacy was documented in 73 of 100 and 72 of 100, meeting noninferiority, with serious adverse events in 40 and 34.

PMID: 40802264
Human2021

Kidney safety against vancomycin

Among 1,325 patients on any dalbavancin regimen, kidney toxicity occurred in 3.7%, against 9.3% of 54 patients given intravenous vancomycin for at least 10 days.

PMID: 33515414
Human2023

Children with skin infections

In a phase 3 open-label study, children from birth to under 18 received single-dose or two-dose dalbavancin or a comparator antibiotic; treatment-emergent adverse events occurred in 7.2% and 9.0% of the dalbavancin groups and 3.3% of comparator patients.

PMID: 36476623
Safety

Side Effects & Contraindications

Reported Side Effects

From the studies above.

● Lower rates of kidney toxicity than prolonged intravenous vancomycin
● Serious adverse events in 40% against 34% on standard therapy in the bloodstream-infection trial

Contraindications & Cautions

Warnings from the Dalvance label (DailyMed, effective January 13, 2025).

● Hypersensitivity reactions
● Infusion-related reactions
● Liver effects
● Clostridioides difficile-associated diarrhoea
● Development of drug-resistant bacteria
Questions

Frequently Asked Questions

?Is dalbavancin a peptide?

Yes, in the broad sense: it is a glycopeptide, a peptide core carrying sugars, modified with a fatty side chain, which is why the class is called lipoglycopeptides.

?How long does one dose of dalbavancin last?

Its effective half-life is about 8.5 days, which is why a skin infection can be treated with a single 1,500 mg infusion or two doses a week apart.

?What is dalbavancin used for?

Acute bacterial skin and skin structure infections caused by susceptible Gram-positive bacteria, in adults and children. It has also been studied for bloodstream infection.

Bibliography

References

  1. [fda] US FDA, Drugs@FDA (openFDA): DALVANCE, NDA 021883 (May 23, 2014). Read October 3, 2026.
  2. [fda-pi] FDA. Dalvance (dalbavancin) US prescribing information (DailyMed set 4b4674d8-4d1e-4728-8465-d42ada33fa5c, effective January 13, 2025). Read October 3, 2026.
  3. [clinical-trial] Boucher HW, et al. "Once-weekly dalbavancin versus daily conventional therapy for skin infection." N Engl J Med, 2014;370(23):2169-79. PMID: 24897082.
  4. [clinical-trial] Turner NA, et al. "Dalbavancin for Treatment of Staphylococcus aureus Bacteremia: The DOTS Randomized Clinical Trial." JAMA, 2025;334(10):866-77. PMID: 40802264.
  5. [pubmed] Gonzalez PL, et al. "Safety of Dalbavancin in the Treatment of Acute Bacterial Skin and Skin Structure Infections (ABSSSI): Nephrotoxicity Rates Compared with Vancomycin: A Post Hoc Analysis of Three Clinical Trials." Infect Dis Ther, 2021;10(1):471-481. PMID: 33515414.
  6. [pubmed] Giorgobiani M, et al. "The Safety and Efficacy of Dalbavancin and Active Comparator in Pediatric Patients With Acute Bacterial Skin and Skin Structure Infections." Pediatr Infect Dis J, 2023;42(3):199-205. PMID: 36476623.

Sources & Citations

Studies were read from their PubMed records; regulatory sources are listed below, read October 3, 2026.

Medical Disclaimer: This content is for educational and informational purposes only. It is not medical advice, and nothing here is an instruction to obtain or use any compound. Consult a licensed healthcare provider before making health decisions.

Last reviewed: 2026-10-03