Barrett J F
Pharmaceutical Research and Development Division, Bristol-Myers Squibb Pharmaceutical Research Institute, Wallingford, CT 06492, USA.
Curr Opin Investig Drugs. 2000 Oct;1(2):181-7.
Linezolid is an oxazolidinone developed by Pharmacia (formerly Pharmacia & Upjohn) for the treatment of multi-resistant Gram-positive infections [187765,317456]. It binds to ribosomal 50S subunits, most likely within domain V within the 23S rRNA peptidyl transferase and a secondary interaction with the 30S subunit. This results in inhibition of the initiation of protein translation at an early point, which is probably N-formylmethionyl-tRNA [335843]. No direct action on DNA or RNA synthesis has been observed [220169]. Linezolid resistance due to a 23S rRNA mutation may emerge in Enterococci during therapy with this antimicrobial, and may be associated with clinical failure [368652]. Following FDA approval, linezolid was launched in May 2000 [368526,368652]. In April 2000, the FDA approved linezolid injection, tablets and oral suspension for the treatment of patients with infections caused by Gram-positive bacteria. It is indicated for adults in the treatment of nosocomial pneumonia, community-acquired pneumonia (CAP), complicated and uncomplicated skin and skin structure infections and vancomycin-resistant enterococcus (VRE) infections caused by methicillin-resistant Staphylococcus aureus (MRSA), VRE faecium and penicillin-susceptible Streptococcus pneumoniae [363503]. The FDA, however, did not grant Pharmacia indications for linezolid in the treatment of CAP due to either penicillin-resistant S aureus (PRSA) or MRSA. In May 2000, Merrill Lynch predicted sales for 2000 to be US $50 million, rising to US $760 million in 2004 [366910]. In February 2000, P&U predicted that peak sales of the drug had the potential to reach in excess of US $750 million [358429]. In February 1999, Morgan Stanley Dean Witter predicted sales of US $40 million in 2000 rising to US $275 million in 2005 [319855]. In December 1998, Deutsche Bank predicted sales of US $100 million in 2000 rising to US $300 million in 2002 [316769].
利奈唑胺是辉瑞公司(原辉瑞制药有限公司)研发的一种恶唑烷酮类药物,用于治疗多重耐药革兰氏阳性菌感染[187765,317456]。它与核糖体50S亚基结合,最有可能在23S核糖体RNA肽基转移酶的结构域V内,并且与30S亚基存在二级相互作用。这导致在早期阶段抑制蛋白质翻译的起始,可能是抑制N-甲酰甲硫氨酰-tRNA[335843]。未观察到对DNA或RNA合成有直接作用[220169]。在使用这种抗菌药物治疗期间,肠球菌可能会因23S rRNA突变而出现利奈唑胺耐药,这可能与临床治疗失败有关[368652]。经美国食品药品监督管理局(FDA)批准后,利奈唑胺于2000年5月上市[368526,368652]。2000年4月,FDA批准利奈唑胺注射剂、片剂和口服混悬液用于治疗由革兰氏阳性菌引起感染的患者。它适用于成人治疗医院获得性肺炎、社区获得性肺炎(CAP)、复杂和非复杂皮肤及皮肤结构感染,以及由耐甲氧西林金黄色葡萄球菌(MRSA)、屎肠球菌VRE和青霉素敏感肺炎链球菌引起的耐万古霉素肠球菌(VRE)感染[363503]。然而,FDA未批准辉瑞公司将利奈唑胺用于治疗由耐青霉素金黄色葡萄球菌(PRSA)或MRSA引起的CAP。2000年5月,美林证券预测2000年的销售额为5000万美元,到2004年将增至7.6亿美元[366910]。2000年2月,辉瑞公司预测该药物的销售峰值有可能超过7.5亿美元[358429]。1999年2月,摩根士丹利添惠预测2000年销售额为4000万美元,到2005年将增至2.75亿美元[319855]。1998年12月,德意志银行预测2000年销售额为1亿美元,到2002年将增至3亿美元[316769]。