Related Experiment Video
Updated: Apr 8, 2026

An Automated Culture System for Use in Preclinical Testing of Host-Directed Therapies for Tuberculosis
Published on: August 16, 2021
Tedizolid: The First Once-Daily Oxazolidinone Class Antibiotic
Steven D Burdette1, Robin Trotman2
1Wright State University Boonshoft School of Medicine, Dayton, Ohio.
Abstract:
Tedizolid phosphate is the second commercially available oxazolidinone antibiotic, although the first one in class that is dosed once daily. It is a prodrug that is rapidly converted to the active compound tedizolid. Tedizolid has activity against a wide range of gram-positive pathogens, including methicillin-resistant Staphylococcus aureus. It is approved to treat acute bacterial skin and skin structure infections (ABSSSIs). In 2 randomized controlled phase 3 trials, 6 days of tedizolid (200 mg once daily) has been proven to be noninferior to 10 days of linezolid (600 mg twice daily). These 2 ABSSSI studies have positioned tedizolid among the growing armamentarium of newer, novel, anti-gram-positive agents. Tedizolid appears to differ from linezolid in the incidence of gastrointestinal and hematologic side effects and appears to lack drug interactions with selective serotonin reuptake inhibitors. Conditions other than ABSSSI are currently being evaluated in clinical studies.
Insights
Tedizolid is a novel oxazolidinone antibiotic approved for skin infections. Clinical trials show it is noninferior to linezolid with a shorter duration and fewer side effects.
Area of Science:
- Pharmacology
- Infectious Diseases
- Clinical Trials
Background:
- Tedizolid phosphate is a once-daily oxazolidinone antibiotic prodrug.
- It is converted to active tedizolid, effective against Gram-positive pathogens like MRSA.
- Tedizolid is approved for acute bacterial skin and skin structure infections (ABSSSI).
Purpose of the Study:
- To evaluate the efficacy and safety of tedizolid in treating ABSSSI.
- To compare tedizolid's effectiveness and side effect profile against linezolid.
Main Methods:
- Two randomized controlled phase 3 trials were conducted.
- Participants received either 6 days of tedizolid (200 mg once daily) or 10 days of linezolid (600 mg twice daily).
Main Results:
- Tedizolid demonstrated noninferiority to linezolid in treating ABSSSI.
- Tedizolid showed a different incidence of gastrointestinal and hematologic side effects compared to linezolid.
- Tedizolid appears to lack drug interactions with SSRIs.
Conclusions:
- Tedizolid is a viable alternative to linezolid for ABSSSI treatment.
- The shorter dosing regimen and potentially improved side effect profile of tedizolid are significant advantages.
- Further studies are evaluating tedizolid for other infections.
More Related Videos
Related Concept Videos
Inhibitors of Bacterial DNA Synthesis
Pulmonary Tuberculosis V
Latent tuberculosis infection occurs when TB bacteria are present in a person's body, but are not causing illness or symptoms. It is not contagious, and preventive treatment is crucial to avoid the...
Pulmonary Tuberculosis IV
Several diagnostic approaches are used to detect TB. The conventional method is the Tuberculin Skin Test (TST), also known as the Mantoux test. However, this method has...
Treating Helicobacter pylori in Peptic Ulcers: Antimicrobial Therapy
Antimicrobial Effectiveness
Dosage Regimen: Multiple Oral Dosage

