|
Lipoglycopeptides are a class of antibiotic that have lipophilic side-chains linked to glycopeptides. The class includes oritavancin, telavancin and dalbavancin. In September 2009 the FDA approved Vibativ (telavancin) for complicated skin and skin structure infections (cSSSI) On May 23, 2014 FDA approved Dalvance (dalbavancin), an injectable drug, administered intravenously in two doses one week apart. On August 6, 2014 FDA approved Orbactiv (oritavancin), an injectable drug administered as a single dose to comprise a full course of therapy. Telavancin is the most potent of the 3 against ''Clostridium spp.'' ==Approvals and clinical trials== Telavancin (once daily injection) has completed 4 phase III trials.〔http://clinicaltrials.gov/ct2/results?term=telavancin&phase=2〕 and gained US FDA approval in September 2009 for complicated skin and skin structure infections (cSSSI). Oritavancin (once daily injection)〔 has completed a phase II trial. 〔http://clinicaltrials.gov/ct2/show/NCT00514527〕 it doesn't have US or European approval for marketing for clinical use. (In December 2008 the FDA declined to approve it, and an EU application was withdrawn.) Oritavancin was approved by the FDA on August 6th, 2014 for treatment of acute bacterial skin and skin structure infections (ABSSSI). 〔http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm408475.htm〕 Dalbavancin (once-weekly injection)〔 was undergoing a phase II trial, due to end in 2003.〔http://clinicaltrials.gov/ct2/show/NCT00057369〕 The FDA approved Dalbavancin for use to treat MRSA infections in adults on May 23rd, 2014. Dalbavancin (Dalvance) is intended to treat acute bacterial skin and skin structure infections (ABSSSI) caused by certain susceptible bacteria like Staphylococcus aureus (including methicillin-susceptible and methicillin-resistant strains) and Streptococcus pyogenes. Dalbavancin is the first drug designated as a Qualified Infectious Disease Product (QIDP) to receive FDA approval. Under the Generating Antibiotic Incentives Now (GAIN) title of the FDA Safety and Innovation Act, Dalvance was granted QIDP designation because it is an antibacterial or antifungal human drug intended to treat serious or life-threatening infections. As part of its QIDP designation, Dalvance was given priority review, which provides an expedited review of the drug’s application. Dalvance’s QIDP designation also qualifies it for an additional five years of marketing exclusivity to be added to certain exclusivity periods already provided by the Food, Drug and Cosmetic Act. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「lipoglycopeptide」の詳細全文を読む スポンサード リンク
|