FDA-approved

Skin & aging

Dalbavancin / Oritavancin / Telavancin

EvidenceFDA approved
ClassLipoglycopeptide antibiotics

Dalbavancin, oritavancin, and telavancin are FDA-approved lipoglycopeptide antibiotics for Gram-positive infections. See how they work and differ.

Reviewed by
William Maish, MD MBA MPH, Clinical Product Lead
Published
October 5, 2026
Last updated
October 5, 2026

Key takeaway

Dalbavancin, oritavancin, and telavancin (sold as Dalvance, Orbactiv, and Vibativ) are lipoglycopeptide antibiotics, semi-synthetic relatives of vancomycin that treat Gram-positive infections, including MRSA. Dalbavancin's half-life of roughly two weeks and oritavancin's single-infusion course allow very infrequent dosing for a skin infection, while telavancin is dosed daily. All three are FDA-approved in the U.S., and they are given intravenously.

At a glance

What they areLipoglycopeptide antibiotics derived from the glycopeptide class, active against Gram-positive bacteria including MRSA
Approved forAcute bacterial skin and skin-structure infections (all three); telavancin also for certain hospital-acquired pneumonia
Key factDalbavancin, given as two once-weekly doses, was non-inferior to a standard vancomycin course for skin infections
RouteIntravenous
Evidence strengthFDA approved

What are dalbavancin, oritavancin, and telavancin?

Dalbavancin (Dalvance), oritavancin (Orbactiv, also Kimyrsa), and telavancin (Vibativ) are lipoglycopeptide antibiotics, semi-synthetic molecules built on the glycopeptide backbone of vancomycin with an added lipid side chain. That modification extends how long they last in the body and, for two of them, adds a second way of attacking bacteria. All three are active against Gram-positive organisms including MRSA. They were approved in the United States between 2009 (telavancin) and 2014 (dalbavancin and oritavancin).

How do they work?

Like vancomycin, these drugs block bacterial cell-wall synthesis by binding the D-alanyl-D-alanine end of the wall's building blocks, preventing the cross-linking that gives the wall strength. The lipid tail anchors them in the bacterial membrane, which both prolongs their activity and, in the case of oritavancin and telavancin, lets them also disrupt the membrane itself, a second bactericidal mechanism. All are bactericidal against Gram-positive bacteria including MRSA.

The standout practical feature is duration. Dalbavancin's half-life of roughly two weeks allows a once-weekly or even single-dose regimen, and oritavancin treats a skin infection with a single infusion. In its pivotal program, once-weekly dalbavancin was non-inferior1 to a conventional vancomycin-to-linezolid course for skin infections. Telavancin is dosed daily and has a broader approved role that includes some pneumonia.

Is it FDA-approved?

Yes. All three are approved for acute bacterial skin and skin-structure infections. The table shows when each was approved and for what:

DrugFDA approvalApproved for
Telavancin2009Acute bacterial skin and skin-structure infections; also hospital-acquired and ventilator-associated bacterial pneumonia due to susceptible S. aureus when alternatives are unsuitable
Dalbavancin2014; extended to children from birth in 2021Acute bacterial skin and skin-structure infections
Oritavancin2014Acute bacterial skin and skin-structure infections

Telavancin carries boxed warnings for kidney toxicity and for fetal risk, requiring a pregnancy test before use.

What are they prescribed for?

These drugs are prescribed for acute bacterial skin and skin-structure infections caused by susceptible Gram-positive bacteria, including MRSA. Dalbavancin and oritavancin are often chosen when a very short or single-dose course is advantageous, such as avoiding a prolonged IV line. Telavancin is also used for certain hospital-acquired pneumonias when other options are not appropriate.

What are the side effects?

According to the prescribing information, common side effects include:

  • Nausea, headache, and diarrhea
  • Rises in liver enzymes (dalbavancin)
  • Taste disturbance and foamy urine (telavancin)

More serious considerations include:

  • Telavancin's boxed warnings for kidney toxicity (with higher mortality in pneumonia patients who already have moderate-to-severe kidney impairment) and for fetal harm
  • Oritavancin interferes with some blood-clotting tests and should not be used with intravenous unfractionated heparin for a period after dosing
  • Infusion-related reactions

More for skin & aging

Sources: FDA prescribing information for Dalvance, Orbactiv, and Vibativ; the DISCOVER dalbavancin trials (Boucher et al., The New England Journal of Medicine, 2014, DOI: 10.1056/NEJMoa13104801), indexed on PubMed. This document is educational and does not constitute medical advice.