eisai and imbrium therapeutics announce u.s. fda filing acceptance of new drug application for lemborexant for the treatment of insomnia-威尼斯人888
tokyo and stamford, conn. – march 12, 2019 – eisai co., ltd. (ceo: haruo naito, "eisai") and imbrium therapeutics l.p. (imbrium therapeutics), a clinical-stage biopharmaceutical company and operating subsidiary of purdue pharma, l.p. (president and ceo: craig landau, md) today announced that the u.s. food and drug administration (fda) has accepted for review the new drug application (nda) for lemborexant, an investigational agent being studied for the treatment of insomnia, a sleep-wake disorder. a prescription drug user fee act (pdufa) date is set for december 27, 2019.
the nda submission was based on data from the clinical development program including two pivotal phase 3 studies of lemborexant – sunrise 1 (study 304) and sunrise 2 (study 303).
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sunrise 1: a one-month phase 3 clinical study to evaluate the efficacy and safety of lemborexant versus placebo and versus an active comparator (zolpidem tartrate extended release, "zolpidem er") in 1,006 patients 55 years and older (45 percent of all patients were aged 65 years and older) with insomnia disorder. this study assessed sleep latency (using latency to persistent sleep; primary objective); sleep efficiency and wake after sleep onset (effect on maintaining sleep; key secondary objectives) objectively using polysomnography, and achieved its primary and key secondary objectives. the most common adverse events (aes) reported in the lemborexant arms were headache and somnolence.1
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sunrise 2: a 12-month placebo-controlled (first six months) phase 3 clinical study to evaluate the long-term efficacy and safety of lemborexant in 949 adult patients (18 to 88 years of age) with insomnia disorder. this study evaluated subjective (patient-reported) sleep onset latency (primary objective), sleep efficiency, and wake after sleep onset (key secondary objectives) using sleep diaries, and achieved its pre-specified primary and key secondary efficacy objectives. the most common aes reported in the lemborexant arms were somnolence, nasopharyngitis, headache, and influenza.2
"our ultimate goal for the development of a sleep-wake treatment is to bring to patients living with insomnia a new option that has the potential to improve their ability to fall asleep, stay asleep and wake the next morning without impairment," said lynn kramer, md, chief clinical officer and chief medical officer, neurology business group, eisai. "this milestone for lemborexant brings us one step closer to addressing unmet needs for millions of patients who experience insomnia."
"insomnia, a disorder of sleep quality and quantity, causes significant impairment in daily functioning and has long-term consequences for health and well-being,"3 said john renger, phd, vice president, head of research & development and regulatory affairs, imbrium therapeutics. "we are committed to working with our partner eisai to make this investigational treatment available to patients, pending regulatory approval."
lemborexant is being jointly developed by eisai and imbrium therapeutics for the treatment of multiple sleep-wake disorders, including insomnia disorder. information about ongoing clinical studies is available at clinicaltrials.gov.
eisai and imbrium therapeutics are striving to address new unmet medical needs and to improve the lives of patients and their families.
this release discusses investigational uses of an agent in development and is not intended to convey conclusions about efficacy or safety. there is no guarantee that such an investigational agent will successfully complete clinical development or gain health authority approval.
contacts:
eisai co., ltd. imbrium therapeutics l.p.
public relations department
81-(0)3-3817-5120
1. about lemborexant
lemborexant is a novel investigational small molecule compound, discovered and developed by eisai in-house scientists, that inhibits orexin signaling by binding competitively to both orexin receptor subtypes (orexin receptor 1 and 2). in individuals with normal daily sleep-wake rhythms, orexin signaling is believed to promote periods of wakefulness. in individuals with sleep-wake disorders, it is possible that orexin signaling that regulates wakefulness is not functioning normally, suggesting that inhibiting inappropriate orexin signaling may enable initiation and maintenance of sleep. eisai and imbrium therapeutics are investigating lemborexant as a potential treatment option for multiple sleep-wake disorders, such as insomnia. additionally, a phase 2 clinical study of lemborexant in patients with irregular sleep-wake rhythm disorder (iswrd) and mild to moderate alzheimer’s dementia is underway.
2. about sunrise 1 (study 304)1
sunrise 1 was a multicenter, randomized, double-blind, placebo-controlled, active comparator, parallel-group study evaluating the efficacy and safety of lemborexant in 1,006 male or female adult patients 55 years and older (45 percent of patients were 65 years and older) with insomnia disorder conducted in north america and europe. sunrise 1 included a pre-randomization phase of up to 35 days (including a two-week placebo run-in period) and a randomization phase comprised of a 30-day treatment period and a minimum two-week period without treatment prior to the end-of-study visit. in this study, patients were randomized to receive placebo or one of three treatment regimens (lemborexant 5 mg, lemborexant 10 mg, zolpidem er 6.25 mg).
the primary objective for sunrise 1 was to demonstrate using polysomnography that lemborexant at either the 5 mg or 10 mg dose is superior to placebo on objective sleep onset, as measured by latency to persistent sleep after the last two nights of one month of treatment. key secondary objectives included change from baseline in sleep efficiency and wake after sleep onset (waso) for both lemborexant doses compared to placebo, and waso in the second half of the night (waso2h) for both lemborexant doses compared to zolpidem er, each after the last two nights of one month of treatment.
3. about sunrise 2 (study 303)2
sunrise 2 was a 12-month multicenter, global, randomized, controlled, double-blind, parallel-group study of the efficacy and safety of lemborexant in 949 male or female adult participants 18 to 88 years of age with insomnia disorder. sunrise 2 included a pre-randomization phase of up to 35 days (including a two-week placebo run-in period) and a randomization phase comprised of a six-month placebo-controlled treatment period, a six-month period of active-only treatment and a two-week period without treatment prior to the end-of-study visit. in this study, during the placebo-controlled treatment period, patients were randomized to receive placebo or one of two treatment regimens (lemborexant 5 mg or 10 mg). during the active-only treatment period, patients who received placebo during the first period were re-randomized to receive lemborexant 5 mg or 10 mg. patients who received active treatment during the first period continued on the treatment to which they were originally randomized.
the primary objective was change from baseline in subjective sleep onset latency after six months of placebo-controlled treatment using patient reported (subjective) sleep diaries. key secondary endpoints were change from baseline in subjective sleep efficiency and subjective wake after sleep onset (swaso) by using patient reported (subjective) sleep diaries for both lemborexant doses after six months of placebo-controlled treatment.
4. about sleep disorders
population studies show that sleep disorders affect many more people worldwide than previously thought.4 insomnia disorder is the most common sleep disorder affecting approximately 30 percent of the adult population worldwide.4,5 insomnia disorder is characterized by difficulty falling asleep, staying asleep or both, despite an adequate opportunity to sleep, which can lead to daytime consequences such as fatigue, difficulty concentrating and irritability.3,6
sleeping well is essential for good health, including brain health. poor sleep is associated with a wide range of health consequences, including an increased risk of hypertension, accidental injury, diabetes, obesity, depression, heart attack, stroke and dementia, as well as adverse effects on mood and behavior.3,7
experimental studies in animals and humans provide evidence of associations between sleep and disease risk factors, diseases and mortality.8 studies suggest an optimal sleep duration between seven and eight hours.9
women are 1.4 times more likely than men to suffer from insomnia.10 older adults also have higher prevalence of insomnia; aging is often accompanied by changes in sleep patterns, including disrupted sleep, frequent waking and early waking, that can lead to less sleep time.11
5. about eisai co., ltd
eisai co., ltd. is a leading global research and development-based pharmaceutical company headquartered in japan. we define our corporate mission as "giving first thought to patients and their families and to increasing the benefits health care provides," which we call our human health care (hhc) philosophy. with over 10,000 employees working across our global network of r&d facilities, manufacturing sites and marketing subsidiaries, we strive to realize our hhc philosophy by delivering innovative products in various therapeutic areas with high unmet medical needs, including neurology and oncology. furthermore, we invest and participate in several partnership-based initiatives to improve access to medicines in developing and emerging countries. for more information about eisai co., ltd., please visit .
6. about imbrium therapeutics
imbrium is a clinical-stage biopharmaceutical company dedicated to advancing medical science through the development of important new pharmacologic and biologic therapeutics. we are pursuing treatments for disorders of the central nervous system, oncology chemotherapeutics, and non-opioid approaches to the management of pain. as an operating subsidiary of purdue pharma l.p., imbrium strives to develop and bring to market new medicines that serve the unmet needs of patients, physicians, and health systems worldwide. we have built a robust and diversified pipeline of investigational drug candidates, and we actively collaborate with industry and academic partners to identify and advance future impactful medicines. for more information, please visit .
references
1 eisai inc. a multicenter, randomized, double-blind, placebo-conrolled, active comparator, parallel-group study of the efficacy and safety of lemborexant in subjects 55 years and older with insomnia disorder. (e2006-g000-304). (clinicaltrials.gov identifier nct02783729). 2018. unpublished data on file.
2 eisai inc. a long-term multicenter, randomized, double-blind, controlled, parallel-group study of the safety and efficacy of lemborexant in subjects with insomnia disorder (e2006-g000-303). (clinicaltrials.gov identifier nct02952820). 2018. unpublished data on file.
3 institute of medicine. sleep disorders and sleep deprivation: an unmet public health problem. washington, dc: national academies press. 2006.
4 ferrie je, et al. sleep epidemiology – a rapidly growing field. int j epidemiol. 2011;40(6):1431–1437.
5 roth t. insomnia: definition, prevalence, etiology and consequences. j clin sleep med. 2007;3(5 suppl):s7–s10.
6 ohayon mm, et al. epidemiology of insomnia: what we know and what we still need to learn. sleep med rev. 2002;6(2):97-111.
7 pase mp, himali jj, grima na, et al. sleep architecture and the risk of incident dementia in the community. neurology. 2017;89(12):1244-1250.
8 cappuccio fp et al. sleep and cardio-metabolic disease. curr cardiol rep. 2017;19:110.
9 cappuccio fp et al. sleep duration and all-cause mortality: a systematic review and meta-analysis of prospective studies. sleep. 2010;33(5):585-592.
10 roth t, et al. prevalence and perceived health associated with insomnia based on dsm-iv-tr; international statistical classification of diseases and related health problems, tenth revision; and research diagnostic criteria/international classification of sleep disorders, second edition criteria: results from the america insomnia survey. biol psychiatry. 2011;69:592– 600.
11 crowley, k. sleep and sleep disorders in older adults. neuropsychol rev. 2011;21(1):41-53.
