| 查看: 547 | 回复: 5 | |||
| 当前主题已经存档。 | |||
[交流]
FDA马上就要批准的新药
|
|||
|
Nuvigil Cephalon Receives Approvable Letter for Nuvigil (armodafinil) FRAZER, Pa., May 1, 2006 -- Cephalon, Inc. announced today that it has received an approvable letter from the U.S. Food and Drug Administration (FDA) for Nuvigil (armodafinil) Tablets. The company submitted a new drug application (NDA) on March 31, 2005, seeking to market Nuvigil for the treatment of excessive sleepiness associated with narcolepsy, obstructive sleep apnea/hypopnea syndrome (OSA/HS) and shift work sleep disorder (SWSD). FDA approval of Nuvigil is contingent upon finalizing the product label. "We are working closely with the FDA to move this application to an approval and expand our offering of wake-promotion choices for patients," said Dr. Paul Blake, Executive Vice President, Worldwide Medical and Regulatory Operations. "Based on the clinical trials, Nuvigil demonstrated a long duration of effect throughout the waking hours and we are excited at the potential to offer broader options to meet the needs of patients and physicians seeking treatment for excessive sleepiness." Armodafinil is a single-isomer formulation of modafinil, the active pharmaceutical ingredient contained in Provigil (modafinil) Tablets [C-IV]. Cephalon submitted data from four double-blind, randomized, placebo-controlled studies of Nuvigil in patients with excessive sleepiness associated with either narcolepsy, OSA/HS or SWSD to FDA for evaluation as part of the NDA. In these studies, Nuvigil was generally well tolerated, with a safety profile consistent with that observed in studies of Provigil. The most common adverse effects observed included headache, nausea, dizziness, insomnia and anxiety. As previously announced, the company submitted additional information to the FDA related to a possible case of Stevens Johnson Syndrome associated with its Sparlon (modafinil) application. In its Nuvigil approvable letter, the FDA indicated that the outcome of its review of this new information will be addressed directly in the label for Nuvigil. About Excessive Sleepiness (Hypersomnolence) Excessive sleepiness, medically known as hypersomnolence, is the primary symptom -- and often the most debilitating feature -- experienced by the millions of Americans who suffer from narcolepsy, OSA/HS, and SWSD. Despite this fact, it is estimated that 50 to 90 percent of the time, health care professionals fail to recognize that these patients are suffering from excessive sleepiness. The defining characteristic of excessive sleepiness is a consistent inability to stay awake and alert enough to safely and successfully accomplish tasks of daily living. Persons experiencing excessive sleepiness who seek medical attention typically complain of fatigue, tiredness, lapses of attention, lack of energy, low motivation, difficulty concentrating, disrupted sleep, snoring or difficulties at work. |
» 猜你喜欢
氨基酸的酰化反应,求大佬解答
已经有0人回复
26年申博——已发SCI6篇
已经有13人回复
药物学论文润色/翻译怎么收费?
已经有143人回复
碱缸的配制
已经有5人回复
新!澳门科技大学诚招2026年秋季药剂学/生物材料方向博士研究生(申请-考核制)
已经有18人回复
澳科大药学院诚招2026年秋季纳米医学/生物材料博士研究生
已经有16人回复
医药口服制剂辅料应用
已经有0人回复
全新推出Tguide®靶向递送方案,突破99% T细胞转染效率
已经有1人回复
Mal-LN29-LNP-mRNA 试剂盒:自带Mal基团,一盒实现抗体筛选与体内靶向验证
已经有0人回复
自由偶联 | 脾脏靶向:抗体偶联空载LNP试剂盒
已经有0人回复
0.5
2楼2006-05-14 11:44:59
3楼2006-05-14 14:04:36
4楼2006-05-16 10:25:58
0.5
| 谢谢分享,赞 |
5楼2006-05-16 10:30:55
6楼2006-05-18 16:52:43












回复此楼