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Single Intravenous Dose of Oritavancin for Treatment of Acute Skin and Skin Structure Infections Caused by Gram-Positive Bacteria: Summary of Safety Analysis from the Phase 3 SOLO Studies.
Corey, G Ralph; Loutit, Jeffery; Moeck, Greg; Wikler, Matthew; Dudley, Michael N; O'Riordan, William.
Affiliation
  • Corey GR; Duke University Medical Center, Durham, North Carolina, USA.
  • Loutit J; The Medicines Company, Parsippany, New Jersey, USA.
  • Moeck G; The Medicines Company, Parsippany, New Jersey, USA greg.moeck@themedco.com.
  • Wikler M; The Medicines Company, Parsippany, New Jersey, USA.
  • Dudley MN; The Medicines Company, Parsippany, New Jersey, USA.
  • O'Riordan W; Sharp Chula Vista Medical Center, Chula Vista, California, USA.
Article in En | MEDLINE | ID: mdl-29358292
Oritavancin is a lipoglycopeptide with bactericidal activity against Gram-positive organisms. Its rapid concentration-dependent bactericidal activity and long elimination half-life allow single-dose treatment of acute bacterial skin and skin structure infections (ABSSSI). SOLO I and SOLO II were randomized, double-blind studies evaluating the efficacy and safety of a single 1,200-mg intravenous (i.v.) dose of oritavancin versus twice-daily i.v. vancomycin for 7 to 10 days in ABSSSI patients. Safety data from both studies were pooled for safety analysis. The database comprised pooled safety data for 976 oritavancin-treated patients and 983 vancomycin-treated patients. The incidences of adverse events, serious adverse events, and discontinuations due to adverse events were similar for oritavancin (55.3, 5.8, and 3.7%, respectively) and vancomycin (56.9, 5.9, and 4.2%, respectively). The median time to onset (3.8 days versus 3.1 days, respectively) and the duration (3.0 days for both groups) of adverse events were also similar between the two groups. The most frequently reported events were nausea, headache, and vomiting. Greater than 90% of all events were mild or moderate in severity. There were slightly more infections and infestations, abscesses or cellulitis, and hepatic and cardiac adverse events in the oritavancin group; however, more than 80% of these events were mild or moderate. Subgroup analyses did not identify clinically meaningful differences in the incidence of adverse events attributed to oritavancin. A single 1,200-mg dose of oritavancin was well tolerated and had a safety profile similar to that of twice-daily vancomycin. The long elimination half-life of oritavancin compared to that of vancomycin did not result in a clinically meaningful delay to the onset or prolongation of adverse events. (This study has been registered at ClinicalTrials.gov under registration no. NCT01252719 and NCT01252732.).
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases, Bacterial / Lipoglycopeptides / Gram-Positive Bacteria Type of study: Clinical_trials Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Antimicrob Agents Chemother Year: 2018 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases, Bacterial / Lipoglycopeptides / Gram-Positive Bacteria Type of study: Clinical_trials Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Antimicrob Agents Chemother Year: 2018 Type: Article Affiliation country: United States