Omadacycline for Acute Bacterial Skin and Skin Structure Infections.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
01 08 2019
Historique:
entrez: 2 8 2019
pubmed: 2 8 2019
medline: 4 8 2020
Statut: ppublish

Résumé

Within the last decade, methicillin-resistant Staphylococcus aureus (MRSA) has emerged as a frequent cause of purulent skin and soft tissue infections. New therapeutic options are being investigated for these infections. We report an integrated analysis of 2 randomized, controlled studies involving omadacycline, a novel aminomethylcycline, and linezolid for the treatment of acute bacterial skin and skin structure infections (ABSSSI). Omadacycline in Acute Skin and Skin Structure Infections Study 1 (OASIS-1) initiated patients on intravenous omadacycline or linezolid, with the option to transition to an oral formulation after day 3. OASIS-2 was an oral-only study of omadacycline versus linezolid. In total, 691 patients received omadacycline and 689 patients received linezolid. Infection types included wound infection in 46.8% of patients, cellulitis/erysipelas in 30.5%, and major abscess in 22.7%. Pathogens were identified in 73.2% of patients. S. aureus was detected in 74.7% and MRSA in 32.4% of patients in whom a pathogen was identified. Omadacycline was noninferior to linezolid using the Food and Drug Administration primary endpoint of early clinical response (86.2% vs 83.9%; difference 2.3, 95% confidence interval -1.5 to 6.2) and using the European Medicines Agency primary endpoint of investigator-assessed clinical response at the posttreatment evaluation. Clinical responses were similar across different infection types and infections caused by different pathogens. Treatment-emergent adverse events, mostly described as mild or moderate, were reported by 51.1% of patients receiving omadacycline and 41.2% of those receiving linezolid. Omadacycline was effective and safe in ABSSSI. NCT02378480 and NCT02877927.

Sections du résumé

BACKGROUND
Within the last decade, methicillin-resistant Staphylococcus aureus (MRSA) has emerged as a frequent cause of purulent skin and soft tissue infections. New therapeutic options are being investigated for these infections.
METHODS
We report an integrated analysis of 2 randomized, controlled studies involving omadacycline, a novel aminomethylcycline, and linezolid for the treatment of acute bacterial skin and skin structure infections (ABSSSI). Omadacycline in Acute Skin and Skin Structure Infections Study 1 (OASIS-1) initiated patients on intravenous omadacycline or linezolid, with the option to transition to an oral formulation after day 3. OASIS-2 was an oral-only study of omadacycline versus linezolid.
RESULTS
In total, 691 patients received omadacycline and 689 patients received linezolid. Infection types included wound infection in 46.8% of patients, cellulitis/erysipelas in 30.5%, and major abscess in 22.7%. Pathogens were identified in 73.2% of patients. S. aureus was detected in 74.7% and MRSA in 32.4% of patients in whom a pathogen was identified. Omadacycline was noninferior to linezolid using the Food and Drug Administration primary endpoint of early clinical response (86.2% vs 83.9%; difference 2.3, 95% confidence interval -1.5 to 6.2) and using the European Medicines Agency primary endpoint of investigator-assessed clinical response at the posttreatment evaluation. Clinical responses were similar across different infection types and infections caused by different pathogens. Treatment-emergent adverse events, mostly described as mild or moderate, were reported by 51.1% of patients receiving omadacycline and 41.2% of those receiving linezolid.
CONCLUSIONS
Omadacycline was effective and safe in ABSSSI.
CLINICAL TRIALS REGISTRATION
NCT02378480 and NCT02877927.

Identifiants

pubmed: 31367742
pii: 5541769
doi: 10.1093/cid/ciz396
pmc: PMC6669297
doi:

Substances chimiques

Anti-Bacterial Agents 0
Tetracyclines 0
omadacycline 090IP5RV8F
Linezolid ISQ9I6J12J

Banques de données

ClinicalTrials.gov
['NCT02378480', 'NCT02877927']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

S23-S32

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.

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Auteurs

Fredrick M Abrahamian (FM)

Department of Emergency Medicine, Olive View-UCLA Medical Center, Sylmar.
David Geffen School of Medicine at University of California Los Angeles.

George Sakoulas (G)

Division of Host-Microbe Systems and Therapeutics, Center for Immunity, Infection and Inflammation, University of California San Diego School of Medicine, La Jolla.

Evan Tzanis (E)

Paratek Pharmaceuticals, Inc., King of Prussia, Pennsylvania.

Amy Manley (A)

Paratek Pharmaceuticals, Inc., King of Prussia, Pennsylvania.

Judith Steenbergen (J)

Paratek Pharmaceuticals, Inc., King of Prussia, Pennsylvania.

Anita F Das (AF)

AD Stats Consulting, Guerneville, California.

Paul B Eckburg (PB)

Paratek Pharmaceuticals, Inc., King of Prussia, Pennsylvania.

Paul C McGovern (PC)

Paratek Pharmaceuticals, Inc., King of Prussia, Pennsylvania.

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Classifications MeSH