news – page 19 – eisai china lnc.-开元体育官网下载手机版

news – page 19 – eisai china lnc.-开元体育官网下载手机版

july 3, 2019 – eisai china inc. announced that it would again donate 350,000 yuan to china population welfare foundation for the project “public welfare stars invite you to help the elderly with cognitive impairment go home”, which was jointly organized by china population welfare foundation and tencent news.

it was reported that this charitable activity will be carried out with “stars appealing and netizens forwarding the appeals”. each forwarding by a participant will bring one “helping hand”, which is equivalent to one yuan donated to the charitable fund, and one yellow bracelet will be donated for every 326 yuan, or 326 times of forwarding. the charitable money will be donated by benevolent enterprises (scan the two-dimensional code below for details of the activity). this activity aims to call public attention to patients with cognitive impairment.

the related funds donated by eisai china inc., one of the benevolent enterprises, will be used to purchase 1,000 positioning yellow bracelets. patients with cognitive impairment and their families can get the yellow bracelets for free in memory clinics of relevant hospitals. the positioning yellow bracelet has the functions of real-time positioning, movement track checking, safety fence, emergency call and so on. families of the elderly can track and positioning the location of the elderly through mobile app, which help change passive search into active care.

cognitive impairment is a progressive declining brain disease, which is often mistaken for normal aging. in addition to the misunderstandings, there is still serious discrimination against the elderly with cognitive impairment in our society. what’s more, such patients have a strong sense of shame, resulting in a low rate of medical treatment. the disease is still incurable up to now, which brings heavy burdens in finance, care-giving and psychology to families of such patients. china sees large population with cognitive impairment and high incidence of the disease with tens of millions of such patients becoming a huge challenge in the aging society.

since entering china market in the 1990s, we have always been adhering to our company philosophy of hhc (human health care), giving our first thoughts to patients and their families, and to increasing the benefits health care provides. we always commit to promoting the progress and development of neuroscience, one of the key treatment fields we focus on.

in 2019, we will continue to cooperate with the china population welfare foundation to promote a total of nearly 200 online and offline activities regarding yellow bracelets, which is expected to benefit more than 10,000 people, as well as large-scale science popularizations and free clinics. meanwhile, we will collect caregiver stories jointly with china association for alzheimer’s disease and carry out online disease education and more activities in cooperation with jd.com. we are willing to work with all sectors of the society to improve the life quality of patients, promote the development of disease-related industries, enhance social understanding and prevention of the disease and actively help improve public policies to address the challenges brought by an ageing society. 

on june 24, 2019, eisai china inc. was invited to participate in the “health to countryside” activity, which was organized by the education, science, health and sports committee of cppc in qinghai province, and donated drugs worth of about rmb 530,000 yuan to the qinghai red cross society, which will be used in the “health to countryside” activity in qinghai province. eisai china has always been adhering to its hhc (human health care) corporate philosophy, actively participating in charitable activities and bearing its social responsibilities. from 2014 to 2019, we have donated medicines worth of about rmb 3 million yuan through the “health to countryside” campaign.


the honorary credential granted eisai china inc.

the “health to countryside” is hosted by the education, science, health and sports committee of cppc and undertook by the chinese pharmaceutical association to provide health assistance to huangzhong county of xining city, guide county of the hainan tibetan autonomous prefecture, gangcha county of haibei tibetan autonomous prefecture and xihai town of haibei prefecture of qinghai province etc. it is an important activity organized annually by the education, science, health and sports committee of cppc and a traditional activity to implement the cppcc constitution, providing not only basic medical services, medicines, concepts, technologies and management, but also charity clinics and lectures etc., which close the distance between the committee members, experts, doctors, enterprises and the masses.

the core of the “hhc” concept of eisai china is to give our first thoughts to patients and their families, actively communicate with patients and meet the needs of both patients and their families. eisai china advocates that every employee should spend 1% of their working time with patients every year to practice hhc. only by understanding the patients’ feelings and pains, we could provide better services, introduce products that the patients really need and win the trust of both the patients and their families on the products and services of eisai china. eisai china attaches great importance to corporate social responsibility and will continue to devote its corporate love to the “health to countryside” under the leadership of ms. feng yanhui, the president of eisai china, and contribute to the medical and health career in the poverty-stricken areas.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that a joint research group including scientists from eisai and professor yoshito kishi’s group of harvard university has achieved a total synthesis and obtained results of nonclinical studies of the novel compound, e7130, derived from total synthesis of halichondrin. these results have been published in scientific reports, a scientific journal of nature.1 currently a phase i study to investigate e7130 in solid tumor is underway in japan.

halichondrins, which was isolated from the marine sponge halichondria okadai in 1986, was known for their outstanding antitumor activity in mice, however the supply from natural sources were limited. furthermore, the very complicated chemical structure has prevented drug discovery and development based on intact halichondrins. the joint research group strictly controlled 31 asymmetric carbons and achieved a total synthesis of e7130, on a >10 g scale with >99.8% purity under gmp (good manufacturing practice) conditions.
the joint research team also demonstrated that e7130 is not only a novel microtubule dynamics inhibitor but can also increase intratumoral cd31-positive endothelial cells (vascular remodeling activity) and reduce alpha-sma (smooth muscle actin)-positive cancer-associated fibroblasts (anti-caf effect), which are important constituents of the tumor microenvironment and may be involved in the malignant transformation of cancers in nonclinical in vivo studies.

according to these unique effects, e7130 augments the effect of antitumor treatments in nonclinical studies. overall, our work demonstrates that a total synthesis can address the issue of limited material supply in drug discovery and development even for complex natural products.

“in 1992, it was unthinkable to synthesize a gram-quantity of a halichondrin,” said yoshito kishi, morris loeb professor of chemistry, emeritus, in the department of chemistry and chemical biology at harvard university, said “but three years ago we proposed it to eisai. organic synthesis has advanced to that level, even with molecular complexity that was untouchable several years ago. we are very delighted to see our basic chemistry discoveries have now made it possible to synthesize this compound at large scale.”

eisai positions oncology as a key therapeutic area, and is aiming to discover revolutionary new medicines with the potential to cure cancer. we will maximize the potential of halichondrins by adding e7130 project to two investigational projects of eisai’s eribulin platform; morab-202 (antibody-drug conjugate with eribulin as the payload) and liposomal formulation of eribulin, as it seeks to contribute further to addressing the diverse needs of, and increasing the benefits provided to, patients with cancer, their families, and healthcare providers.

* harvard has exclusively licensed the intellectual property associated with this research project to eisai for the commercial development of therapeutics.


media inquiries:
public relations department,
eisai co., ltd.
81-(0)3-3817-5120

 

[notes to editors]
about e7130
e7130 is a next-generation agent improving tumor microenvironment, which has been developed by a joint research with eisai and harvard university. e7130 is derived from total synthesis of halichondrin, a natural product isolated from the marine sponge halichondria okadai. e7130 is believed to improve tumor microenvironment by unique action for potential effect on immune activation by releasing hypoxia and suppressing interaction between cancer cells and stroma. a phase i study to investigate e7130 in solid tumor is currently underway in japan.

 

1. kawano s et al., “a landmark in drug discovery based on complex natural product synthesis” scientific reports 2019.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that the latest data on its antiepileptic drug (aed) perampanel (product name: fycompa®) will be presented at the 33rd international epilepsy congress (iec) to be held from june 22 to 26, 2019 in bangkok, thailand.

as major presentations, 2 oral presentations will be given including on the final analysis of a phase iii clinical study (study 311) on adjunctive perampanel in pediatric patients aged 4 to less than 12 years old with epilepsy. also, a total of 12 poster presentations will be given, including on the primary analysis from a phase iii clinical study (freedom / study 342), which was conducted in japan and south korea, on the efficacy and safety of perampanel monotherapy in untreated epilepsy patients with partial-onset seizures (with or without secondary generalized seizures).

perampanel is a first-in-class aed and a once-daily tablet discovered at eisai’s tsukuba research laboratories. in the united states and europe, an oral suspension formulation has been approved and is being marketed. the agent is a highly selective, noncompetitive ampa receptor antagonist that reduces neuronal hyperexcitation by targeting glutamate activity at ampa receptors on postsynaptic membranes. perampanel is currently approved in countries around the world as an adjunctive therapy for the treatment of partial-onset seizures (with or without secondary generalized seizures) and primary generalized tonic-clonic seizures in patients with epilepsy 12 years of age and older. furthermore, in the united states, perampanel is approved for monotherapy and adjunctive use in the treatment of partial-onset seizures (with or without secondary generalized seizures) in patients with epilepsy 4 years of age and older.

eisai considers neurology including epilepsy, a therapeutic area of focus, and strives to deliver perampanel throughout the world in pursuit of our mission to provide “seizure freedom” to a greater number of patients living with epilepsy. eisai seeks to address the diverse needs of, as well as increasing the benefits provided to, patients with epilepsy and their families.

 

oral presentations

presentation number and scheduled presentation date (local time) abstract title
platform session: treatment

oral presentation:

monday, june 24th 15:30-15:45

safety and efficacy of adjunctive perampanel in paediatric patients (aged 4 to <12 years) with partial-onset seizures (pos) or primary generalised tonic-clonic seizures (pgtcs): final results from the 311 core study
platform session: treatment

oral presentation:

monday, june 24th 15:45-16:00

effect of concomitant enzyme-inducing anti-seizure drugs (eiasds) on the safety and efficacy of adjunctive perampanel in patients aged 4 to <12 years with partial-onset seizures (pos): final results from the 311 core study


poster presentations

presentation number and scheduled presentation date (local time) abstract title
poster # p125

poster session: drug therapy 1

poster presentation:

sunday, june 23rd 10:00-17:00

first-line perampanel added to monotherapy in patients with partial-onset seizures, with or without secondary generalised seizures: a multicentre, open-label, prospective cohort study
poster # p215

poster session: paediatric epileptology 1

poster presentation:

sunday, june 23rd 10:00-17:00

adjunctive perampanel in pediatric patients with epilepsy:

population pharmacokinetic (pk) and exposure-response analyses

poster # p317

poster session: drug therapy 2

poster presentation:

monday, june 24th 10:00-17:00

perampanel does not worsen myoclonic and absence seizures
poster # p328

poster session: drug therapy 2

poster presentation:

monday, june 24th 10:00-17:00

perampanel in real-world clinical care of patients with epilepsy: retrospective phase iv study 506 (prove study)
poster # p329

poster session: drug therapy 2

poster presentation:

monday, june 24th 10:00-17:00

study 506 (prove study) – a retrospective, phase iv study of perampanel in real-world clinical care of patients with epilepsy: adolescent subgroup (aged 12 to <18 years)
poster # p331

poster session: drug therapy 2

poster presentation:

monday, june 24th 10:00-17:00

efficacy and safety of adjunctive perampanel in chinese patients with partial-onset seizures or primary generalised tonic-clonic seizures: post hoc analysis of phase iii double-blind and open-label extension studies
poster # p410

poster session:

paediatric epileptology 2

poster presentation:

monday, june 24th 10:00-17:00

safety and efficacy of adjunctive perampanel in younger (aged 4 to < 7 years) and older (7 to < 12 years) paediatric patients with partial-onset seizures (pos) or primary generalised tonic-clonic seizures (pgtcs): final results from the 311 core study
poster # p413

poster session:

paediatric epileptology 2

poster presentation:

monday, june 24th 10:00-17:00

study 506 (prove study) – a retrospective, phase iv study of perampanel in real-world clinical care of patients with epilepsy: paediatric subgroup (aged <12 years)
poster # p424

poster session:

paediatric epileptology 2

poster presentation:

monday, june 24th 10:00-17:00

effect of adjunctive perampanel on clinical global impression (cgi) in paediatric patients (aged 4 to <12 years) with partial-onset seizures (pos) or primary generalised tonic-clonic seizures (pgtcs) in study 311
poster # p425

poster session:

paediatric epileptology 2

poster presentation:

monday, june 24th 10:00-17:00

safety and efficacy of adjunctive perampanel in japanese paediatric patients (aged 4 to < 12 years) with partial-onset seizures (pos) with or without secondarily generalised seizures (sgs):

final results from the 311 core study

poster # p315

poster session: drug therapy 3

poster presentation:

tuesday, june 25th 10:00-17:00

efficacy and safety of perampanel monotherapy in previously untreated patients with partial-onset seizures (pos):

primary analysis of study 342 (freedom study)

poster # p520

poster session: drug therapy 3

poster presentation:

tuesday, june 25th 10:00-17:00

efficacy and safety of adjunctive perampanel in indian patients with partial-onset seizures (pos) or primary generalised tonic-clonic seizures (pgtcs): post hoc analysis of phase ii and iii double-blind and open-label extension (olex) studies

 

media inquiries:
public relations department,
eisai co., ltd.
81-(0)3-3817-5120

 

[notes to editors]
1.  about perampanel (generic name, product name: fycompa) 
perampanel is a first-in-class aed discovered and developed by eisai. with epileptic seizures being mediated by the neurotransmitter glutamate, the agent is a highly selective, noncompetitive ampa receptor antagonist that reduces neuronal hyperexcitation by targeting glutamate activity at ampa receptors on postsynaptic membranes. perampanel is available in tablet form to be taken once daily orally at bedtime. in addition, an oral suspension formulation has been approved and is being marketed in the united states and europe.

perampanel is currently approved in more than 55 countries, including the united states, japan, in europe and in asia as adjunctive treatment for partial-onset seizures (with or without secondarily generalized seizures) in patients with epilepsy 12 years of age and older. an application seeking approval for use in the adjunctive treatment of partial-onset seizures is under review in china, which has been designated for priority review. in addition, perampanel has been approved in more than 50 countries, including the united states, japan, in europe and in asia for treatment as an adjunctive therapy for tonic-clonic seizures in patients with generalized epilepsy 12 years of age and older. in the united states, perampanel is approved for monotherapy and adjunctive use in the treatment of partial-onset seizures (with or without secondarily generalized seizures) in patients with epilepsy 4 years of age and older. in japan, a supplementary new drug application has been filed seeking approval of perampanel for use as monotherapy for partial-onset seizures, treatment for partial-onset seizures in pediatric patients aged 4 years and older, as well as a fine granule formulation. in europe, an application has been submitted seeking the additional approval of perampanel for adjunctive use in the treatment of partial-onset seizures (with or without secondarily generalized seizures) or primarily generalized tonic-clonic seizures in pediatric patients with epilepsy.

furthermore, eisai is conducting a global phase iii clinical study (study 338) for the agent in patients with epileptic seizures associated with lennox-gastaut syndrome.

eisai co.,ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) today announced that latest information on lemborexant, an investigational sleep-wake regulation agent being studied for the treatment of multiple sleep-wake disorders, including insomnia and irregular sleep-wake rhythm disorder (iswrd) will be presented at the 33rd annual meeting of the associated professional sleep societies (sleep 2019), from june 8 to 12 in san antonio, texas, the united states.

eight posters including the integrated analysis of lemborexant’s effects on daily function and disease severity as well as sleep onset and sleep maintenance for the combined 1,955 patient population of two pivotal clinical phase iii studies, sunrise 1 (study 304) and sunrise 2 (study 303) in insomnia disorders, and an evaluation of results on respiratory function after administration of lemborexant in elderly and mild obstructive sleep apnea, and the latest pre-clinical data on iswrd will be presented.

lemborexant acts on the orexin neurotransmitter system and is believed to regulate sleep and wake by controlling arousal without affecting awakening by external stimuli, and is being developed for the treatment of multiple sleep-wake disorders including insomnia disorder. in december 2018 and march 2019, new drug applications seeking approval of lemborexant for use in the treatment of insomnia disorder were submitted in the united states and japan, respectively. for the ongoing clinical studies, please visit clinicaltrials.gov.

through the development of lemborexant, eisai is aiming to bring to patients suffering from sleep-wake disorders a new treatment option to improve their ability to fall and stay asleep and wake without impairing the next morning, and is striving to further contribute to satisfying unmet medical needs and improve the benefits to patients and their families.

 

■ presentations for lemborexant:

poster session: p18, presentation date: monday june 10, 5:15pm – 7:15pm (local time)

presentation title
poster number: 102

abstract: 0367

lemborexant treatment for insomnia: six-month safety
poster number: 105

abstract: 0368

efficacy and tolerability of lemborexant in female and male subjects with insomnia
poster number: 106

abstract: 0369

effect of lemborexant on sleep architecture in older adults with insomnia disorder
poster number: 107

abstract: 0370

patient-reported sleep onset and sleep maintenance: pooled analyses of lemborexant phase 3 studies
poster number: 108

abstract: 0371

lemborexant treatment for insomnia in phase 3: impact on disease severity
poster number: 103

abstract: 0429

respiratory safety of lemborexant in adult and elderly subjects with mild obstructive sleep apnea
poster number: 104

abstract: 0430

respiratory safety of lemborexant in healthy adult and elderly subjects
poster number: 022

abstract: 0056

samp8 mice as a preclinical model for irregular sleep-wake rhythm disorder and efficacy of the dual orexin (hypocretin) receptor antagonist lemborexant

separate from the poster presentations, eisai will host a symposium, an interactive dialogue on insomnia diagnostic and therapeutic decision making, which will be held on sunday, june 9, from 6:15pm – 8:30pm (local time).

 

media inquiries:
public relations department,
eisai co., ltd.
81-(0)3-3817-5120

 

[notes to editors]

1. about lemborexant

lemborexant is a novel investigational small molecule compound, discovered and developed by eisai, that inhibits orexin signaling by binding competitively to both orexin receptor subtypes (orexin receptors 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 is 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 sleep disorders

several population studies show that sleep disorders affect many more people worldwide than previously thought.1 insomnia disorder is the most common sleep disorder, with persistent insomnia symptoms experienced by approximately 30 percent of the adult population.1,2 insomnia disorder is characterized by difficulty falling asleep, staying asleep, or both, despite an adequate opportunity to sleep, that can lead to daytime consequences such as fatigue, difficulty concentrating and irritability.3,4

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, dementia, as well as adverse effects on mood and behavior.3,5

experimental studies in animals and humans provide evidence of associations between sleep and disease risk factors, diseases, and mortality.6 studies suggest an optimal sleep duration between seven and eight hours.7

women are 1.4 times more likely than men to suffer from insomnia.8 older adults also have higher prevalence of insomnia; aging is often accompanied by changes in sleep patterns, including disrupted sleep, frequent walking, and early waking, that can lead to less sleep time.9

1 ferrie je, et al. sleep epidemiology – a rapidly growing field. int j epidemiol. 2011;40(6):1431–1437.
2 roth t. insomnia: definition, prevalence, etiology and consequences. j clin sleep med. 2007;3(5 suppl):s7–s10.
3 institute of medicine. sleep disorders and sleep deprivation: an unmet public health problem. washington, dc: national academies press. 2006.
4 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.
5 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.
6 cappuccio fp et al. sleep and cardio-metabolic disease. curr cardiol rep. 2017;19:110.
7 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.
8 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.
9 crowley, k. sleep and sleep disorders in older adults. neuropsychol rev. 2011;21(1):41-53.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that presentations on a series of abstracts highlighting updates regarding its in-house discovered lenvatinib mesylate (product name: lenvima®, “lenvatinib”, kinase inhibitor), eribulin mesylate (product name: halaven®, “eribulin”, halichondrin class microtubule dynamics inhibitor), and morab-202 (antibody drug conjugate, adc) will be given at the 55th annual meeting of the american society of clinical oncology (asco), taking place in chicago, the united states, from may 31 to june 4, 2019. the latest information on h3b-6527 (fibroblast growth factor receptor 4 inhibitor) and h3b-6545 (selective estrogen receptor α covalent antagonist), which were discovered by eisai’s u.s. oncology precision medicine-focused research and development subsidiary h3 biomedicine inc., will also be highlighted in presentations at asco.

major poster presentations at this year’s meeting include highlights of the latest data from an ongoing phase i clinical study investigating eisai’s first adc morab-202 in patients with solid tumors in japan. morab-202 is a novel adc that combines eisai’s investigational anti-folate receptor α (fra) antibody farletuzumab with eisai’s in-house discovered anticancer agent eribulin as the payload.

eisai positions oncology as a key therapeutic area, and is aiming to discover revolutionary new medicines with the potential to cure cancer. the company will continue to create innovation in the development of new drugs based on cutting-edge cancer research, as it seeks to contribute further to addressing the diverse needs of, and increasing the benefits provided to, patients with cancer, their families, and healthcare providers.

 

major poster presentations:

product abstract title and scheduled presentation date and time (local time)
lenvatinib

 

abstract no: 6081

influence of tumor size and eastern cooperative oncology group performance status (ecog ps) at baseline on patient (pt) outcomes in lenvatinib-treated radioiodine-refractory differentiated thyroid cancer (rr-dtc)

poster presentation | june 1 (sat), 1:15-4:15 pm

lenvatinib

abstract no: tps5607

a phase 3 trial evaluating efficacy and safety of lenvatinib in combination with pembrolizumab in patients with advanced endometrial cancer

poster presentation | june 1 (sat), 1:15-4:15 pm

lenvatinib

abstract no: tps9118

randomized, double-blind, phase 3 trial of first-line pembrolizumab platinum doublet chemotherapy (chemo) ± lenvatinib in patients (pts) with metastatic nonsquamous non-small-cell lung cancer (nsclc): leap-006

poster presentation | june 2 (sun), 8:00-11:00 am

lenvatinib

abstract no: tps4152

lenvatinib (len) plus pembrolizumab (pembro) for the first-line treatment of patients (pts) with advanced hepatocellular carcinoma (hcc): phase 3 leap-002 study

poster presentation | june 3 (mon), 8:00-11:00 am

lenvatinib

abstract no: tps9594

lenvatinib (len) plus pembrolizumab (pembro) in patients (pts) with advanced melanoma previously exposed to anti–pd-1/pd-l1 agents: phase 2 leap-004 study

poster presentation | june 3 (mon), 8:00-11:00 am

eribulin

abstract no: 2606

balixafortide (a cxcr4 antagonist) eribulin in her2 negative metastatic breast cancer (mbc): survival outcomes of the phase 1 trial

poster presentation | june 1 (sat), 8:00-11:00 am

morab-202

abstract no: 5544


first-in-human (fih) phase 1 (ph1) study of morab-202 in patients (pts) with advanced folate receptor alpha (fra)-positive solid tumors

poster presentation | june 1 (sat), 1:15-4:45 pm

h3b-6545

abstract no: 1052

molecular characterization and monitoring of patient ctdna in phase 1 study of h3b-6545 in er mbc

poster presentation | june 2 (sun), 8:00-11:00 am

h3b-6545

abstract no: 1059

phase 1 dose escalation of h3b-6545, a first-in-class highly selective erα covalent antagonist (serca), in women with er-positive, her2-negative breast cancer (hr bc)

poster presentation | june 2 (sun), 8:00-11:00 am

h3b-6527

abstract no: 4095

a phase 1 study of h3b-6527 in hepatocellular carcinoma (hcc) or intrahepatic cholangiocarcinoma (icc) patients (pts)

poster presentation | june 3 (mon), 8:00-11:00 am

h3b-6527

abstract no: 4121

h3b-6527 clinical biomarker assay development and characterization of hcc patient samples

poster presentation | june 3 (mon), 8:00-11:00 am

media inquiries:
public relations department,
eisai co., ltd.

 

[notes to editors]
1. about the eisai and merck & co., inc., kenilworth, n.j., u.s.a. strategic collaboration
in march 2018, eisai and merck & co., inc., kenilworth, n.j., u.s.a., known as msd outside the united states and canada, through an affiliate, entered into a strategic collaboration for the worldwide co-development and co-commercialization of lenvima® (lenvatinib). under the agreement, the companies will jointly develop, manufacture and commercialize lenvima, both as monotherapy and in combination with merck & co., inc., kenilworth, n.j., u.s.a.’s anti-pd-1 therapy keytruda®(pembrolizumab).

in addition to ongoing clinical studies evaluating the lenvima and keytruda combination across several different tumor types, including renal cell carcinoma, the companies will jointly initiate new clinical studies through the leap (lenvatinib and pembrolizumab) clinical program, which will evaluate the combination to support 11 potential indications in six types of cancer (endometrial cancer, hepatocellular carcinoma, melanoma, non-small cell lung cancer, squamous cell carcinoma of the head and neck, and urothelial cancer). the leap clinical program also includes a new basket trial targeting six additional cancer types (biliary tract cancer, breast cancer, colorectal cancer, gastric cancer, glioblastoma and ovarian cancer). the lenvima and keytruda combination is not approved in any cancer types today.

keytruda® is a registered trademark of merck sharp & dohme corp., a subsidiary of merck & co., inc., kenilworth, n.j., usa.

eisai to continue to develop and commercialize lemborexant globally

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announces today that its u.s. subsidiary eisai inc. has bought out purdue pharma l.p.’s rights in the worldwide collaboration for the development and commercialization of lemborexant, an investigational sleep-wake regulation agent being studied for the treatment of multiple sleep-wake disorders, including insomnia and irregular sleep-wake rhythm disorder (iswrd) in patients with alzheimer’s disease. eisai group will solely conduct the development and the commercialization of lemborexant globally.

discovered by eisai, lemborexant is an investigational dual orexin receptor antagonist. the u.s. food and drug administration (fda) accepted the new drug application (nda) for lemborexant for use in the treatment of insomnia disorders for review in march 2019 and set a prescription drug user fee act (pdufa) date for december 27, 2019. for japan, a marketing authorization application for lemborexant for use in the treatment of insomnia disorder has been submitted to the pharmaceuticals and medical devices agency (pmda) in march 2019 and is currently under review. furthermore, a phase ii clinical study of lemborexant for iswrd in patients with alzheimer’s disease is ongoing.

through lemborexant, eisai is striving to address unmet medical needs and contribute to further increasing the benefits for patients with sleep disorders and their families.

media inquiries:
public relations department,
eisai co., ltd.
81-(0)3-3817-5120

  

[notes to editors]
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. 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.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that the latest data on its dual orexin receptor antagonist lemborexant and its antiepileptic drug (aed) perampanel (product name: fycompa®) will be presented at the 2019 annual american academy of neurology (aan) meeting to be held from may 4 to 10, 2019 in philadelphia, pennsylvania in the united states.

as major presentations, an oral presentation will be given on the next-morning residual effects of lemborexant from the results of three placebo-controlled, active comparator, randomized, double-blind clinical studies evaluating on-road driving performance as well as postural stability, and memory and attention performance directly after awakening.
regarding perampanel, a total of 18 poster presentations will be given, including on the final analysis results from a phase iii clinical study (study 311) in pediatric patients aged 4 to 12 years old with epilepsy, as well as on inpatient hospitalization risk in patients with epilepsy before and after perampanel treatment.

eisai considers neurology a therapeutic area of focus, and strives to maximize the value of lemborexant and perampanel to further contribute to addressing the diverse needs of, as well as increasing the benefits provided to, patients and their families.

oral presentation: 

presentation number and scheduled presentation date (local time) abstract title
session 46:sleep science and therapy updates

thursday may 9
poster presentation: 13:00-15:00

effects of lemborexant in the morning: results from 3 randomized studies


poster presentation: 

poster number and scheduled presentation date (local time) abstract title

poster number: 5-009

poster session: p1
sun
day may 5
poster presentation: 17:30-18:30

symptoms and impacts in epilepsy: findings from qualitative patient interviews

poster number: 5-021

poster session: p1
sun
day may 5
poster presentation: 17:30-18:30

safety and efficacy of adjunctive perampanel in younger (aged 4 to <7 years) and older (7 to <12 years) pediatric patients with partial-onset seizures (pos) or primary generalized tonic-clonic seizures (pgtcs) : final results from the 311 core study

poster number: 5-024

poster session: p1
sun
day may 5
poster presentation: 17:30-18:30

a post-marketing observational study to evaluate the safety and tolerability of perampanel as add-on therapy in patients with epilepsy aged ≥12 years

poster number: 5-029

poster session: p1
sun
day may 5
poster presentation: 17:30-18:30

pharmacokinetic (pk) assessment of perampanel intravenous (iv) formulation as a bioequivalent alternative to oral tablet administration

poster number: 5-001

poster session: p3
tues
day may 7
poster presentation: 17:30-18:30

safety and efficacy of adjunctive perampanel in pediatric patients (aged 4 to <12 years) with partial-onset seizures (pos) or primary generalized tonic-clonic seizures (pgtcs): final results from the 311 core study

poster number: 5-002

poster session: p3
tuesday
 may 7
poster presentation: 17:30-18:30

risk of hospitalization in patients with uncontrolled epilepsy treated with a long versus short half-life adjunctive antiepileptic medication

poster number: 5-005

poster session: p3
tues
day may 7
poster presentation: 17:30-18:30

perampanel use in established, refractory, and super-refractory status epilepticus (se): a summary of cases from austria, finland, germany, and spain

poster number: 5-007

poster session: p3
tues
day may 7
poster presentation: 17:30-18:30

effect of concomitant enzyme-inducing antiepileptic drugs (eiaeds) on the safety and efficacy of adjunctive perampanel in patients aged 4 to <12 years with partial-onset seizures (pos): final results from the 311 core study

poster number: 5-017

poster session: p3
tues
day may 7
poster presentation: 17:30-18:30

phase ii, open-label pharmacokinetic (pk) study of perampanel oral suspension as adjunctive therapy in pediatric patients (aged ≥1 to <24 months) with epilepsy: study 238 design and preliminary safety data
poster number: 5-018

poster session: p3
tuesday
 may 7
poster presentation: 17:30-18:30

inpatient hospitalizations rates in patients diagnosed with epilepsy and treated with perampanel or lacosamide
poster number: 5-019

poster session: p3
tues
day may 7
poster presentation: 17:30-18:30

study 410 enrollment update: multicenter, open-label, phase iv study of perampanel as monotherapy or first adjunctive therapy in patients with partial-onset seizures (pos) or primary generalized tonic-clonic seizures (pgtcs)
poster number: 5-022

poster session: p3
tuesday may 7
poster presentation: 17:30-18:30

inpatient hospitalization risk in patients with epilepsy before and after perampanel treatment
poster number: 5-027

poster session: p3
tuesday
 may 7
poster presentation: 17:30-18:30

elevated healthcare burden amongst patients with active generalized tonic-clonic (gtc) convulsions
poster number: 5-004

poster session: p5
thursday
may 9
poster presentation: 17:30-18:30

adjunctive perampanel in pediatric patients with epilepsy: population pharmacokinetic (pk) and exposure-response analyses
poster number: 5-008

poster session: p5
thurs
daymay 9
poster presentation: 17:30-18:30

perampanel in real-world clinical care of patients with epilepsy: retrospective phase iv study 506 – second interim analysis
poster number: 5-009

poster session: p5
thurs
daymay 9
poster presentation: 17:30-18:30

study 506 – second interim analysis of a retrospective, phase iv study of perampanel in real-world clinical care of patients with epilepsy: pediatric subgroup (aged <12 years)
poster number: 5-014

poster session: p5
thursday
may 9
poster presentation: 17:30-18:30

inpatient hospitalization risk in medicaid patients with epilepsy before and after perampanel treatment
poster number: 5-017

poster session: p5
thursd
aymay 9
poster presentation: 17:30-18:30

study 506 – second interim analysis of a retrospective, phase iv study of perampanel in real-world clinical care of patients with epilepsy: adolescent subgroup (aged 12 to <18 years)

 

media inquiries:
public relations department,
eisai co., ltd.
81-(0)3-3817-5120

 

[notes to editors]
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. 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 perampanel (generic name, product name: fycompa)
perampanel is a first-in-class aed discovered and developed by eisai. with epileptic seizures being mediated by the neurotransmitter glutamate, the agent is a highly selective, noncompetitive ampa receptor antagonist that reduces neuronal hyperexcitation associated with seizures by targeting glutamate activity at ampa receptors on postsynaptic membranes. perampanel is available in tablet form to be taken once daily orally at bedtime. in addition, an oral suspension formulation has been approved in the united states.

perampanel is currently approved in more than 55 countries and territories, including the united states, japan, in europe and in asia as adjunctive treatment for partial-onset seizures (with or without secondarily generalized seizures) in patients with epilepsy 12 years of age and older. an application seeking approval for use in the adjunctive treatment of partial-onset seizures is under review in china, which has been designated for priority review. in addition, perampanel has been approved in more than 50 countries, including the united states, japan, in europe and in asia for treatment as an adjunctive therapy for tonic-clonic seizures in patients with generalized epilepsy 12 years of age and older. in the united states, perampanel is approved for monotherapy and adjunctive use in the treatment of partial-onset seizures (with or without secondarily generalized seizures) in patients with epilepsy 4 years of age and older. in japan, a supplementary new drug application has been filed seeking approval of perampanel for use as monotherapy for partial-onset seizures, treatment for partial-onset seizures in pediatric patients aged 4 years and older, as well as a fine granule formulation. in europe, an application has been submitted seeking the additional approval of perampanel for adjunctive use in the treatment of partial-onset seizures (with or without secondarily generalized seizures) or primarily generalized tonic-clonic seizures in pediatric patients with epilepsy.

furthermore, eisai is conducting a global phase iii clinical study (study 338) for the agent in patients with epileptic seizures associated with lennox-gastaut syndrome.

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that in the 8th meeting of the data safety monitoring board (dsmb) for the global phase iii clinical studies (mission ad) on the investigational oral bace (beta amyloid cleaving enzyme) inhibitor elenbecestat (development code: e2609) in early alzheimer’s disease (ad), the dsmb reviewed safety data including the potential for decline in cognition, and recommended the continuation of the studies. elenbecestat is being jointly developed by eisai and biogen inc. (headquarters: cambridge, massachusetts, united states).

the phase iii clinical trial program for elenbecestat (mission ad) consists of two global phase iii clinical studies with identical protocols, mission ad1 (study 301) and mission ad2 (study 302). both studies are multicenter, placebo-controlled, double-blind, parallel-group phase iii clinical studies aiming to assess the efficacy and safety of elenbecestat for treatment in patients with mild cognitive impairment (mci) due to ad or mild ad dementia (collectively known as early ad) with confirmed amyloid pathology in the brain. patients are allocated randomly to receive either 50 mg of elenbecestat or placebo daily during the treatment period of 24 months, and the primary endpoint utilizes the clinical dementia rating sum of boxes (cdr-sb).
enrollment in mission ad is scheduled to be completed in march 2019.

eisai aims to create innovative medicines for alzheimer’s disease as soon as possible in order to further contribute to addressing the unmet medical needs of, as well as potentially increasing the benefits provided to, patients and their families.

 

media inquiries:
public relations department,
eisai co., ltd.
81-(0)3-3817-5120

 

[notes to editors]
1. about elenbecestat (generic name, development code: e2609)
discovered by eisai, elenbecestat is an investigational next-generation oral candidate for the treatment of alzheimer’s disease (ad) that inhibits bace (beta amyloid cleaving enzyme). by inhibiting bace, a key enzyme in the production of aβ peptides, elenbecestat reduces aβ production, and by reducing amyloid plaque formations in the brain, exerts disease modifying effects of potentially slowing the progression of ad. currently, two global phase iii clinical studies (mission ad1/2) of elenbecestat in early ad including mild cognitive impairment (mci) due to ad or the mild ad are underway. in addition, the u.s. food and drug administration (fda) has granted fast track designation for the development of elenbecestat, a process allowing priority reviews by the fda for drugs deemed as having potential to treat serious conditions and tackle key unmet medical needs.

  

2. about mission ad
initiated in october 2016, the phase iii clinical trial program for elenbecestat (mission ad) consists of two global phase iii clinical studies with identical protocols, mission ad1 (study 301) and mission ad2 (study 302), and is being conducted at over 400 sites in 30 countries worldwide. both studies are multicenter, placebo-controlled, double-blind, parallel-group phase iii clinical studies aiming to assess the efficacy and safety of elenbecestat for treatment in patients with mild cognitive impairment (mci) due to ad or mild ad dementia (collectively known as early ad) with confirmed amyloid pathology in the brain. patients are allocated randomly to receive either 50 mg of elenbecestat or placebo daily during the treatment period of 24 months, and the primary endpoint utilizes the clinical dementia rating sum of boxes (cdr-sb).

eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced that a global phase iii clinical study (clarity ad/study 301) of ban2401, an anti-amyloid beta protofibril antibody, in patients with early alzheimer’s disease has been initiated. ban2401 is being jointly developed by eisai and biogen inc. (headquarters: cambridge, massachusetts, united states, “biogen”).

clarity ad is a global placebo-controlled, double-blind, parallel-group, randomized study in 1,566 patients with mild cognitive impairment (mci) due to alzheimer’s disease (ad) or mild alzheimer’s disease dementia (collectively known as early ad) with confirmed amyloid pathology in the brain. after discussion with regulatory agencies based on the results of a phase ii clinical study (study 201), a single phase iii clinical study is being initiated to support a filing for ban2401. the treatment group will be administered a dosage of 10 mg/kg bi-weekly of ban2401, with patients allocated in a 1:1 ratio to receive either placebo or the treatment group. the primary endpoint is the change from baseline in the clinical dementia rating–sum of boxes (cdr-sb) at 18 months of treatment. respective changes from baseline to 18 months of treatment in the ad composite score (adcoms), ad assessment scale–cognitive subscale (adas-cog), and brain amyloid levels as measured by amyloid positron emission tomography (pet) have been set as key secondary endpoints.

eisai aims to create innovative medicines for alzheimer’s disease as soon as possible in order to further contribute to addressing the unmet medical needs of, as well as potentially increasing the benefits provided to, patients and their families.

 

media inquiries:
public relations department,
eisai co., ltd.
81-(0)3-3817-5120

 

[notes to editors]
1. about ban2401
ban2401 is a humanized monoclonal antibody for alzheimer’s disease that is the result of a strategic research alliance between eisai and bioarctic. ban2401 selectively binds to neutralize and eliminate soluble, toxic aβ aggregates (protofibril) that are thought to contribute to the neurodegenerative process in alzheimer’s disease. as such, ban2401 may have the potential to have an effect on disease pathology and to slow down the progression of the disease. eisai obtained the global rights to study, develop, manufacture and market ban2401 for the treatment of alzheimer’s disease pursuant to an agreement concluded with bioarctic in december 2007. in march 2014 eisai and biogen entered into a joint development and commercialization agreement for ban2401 and the parties amended that agreement in october 2017.

2. about study 201
study 201 is a placebo-controlled, double-blind, parallel-group, randomized phase ii clinical study in 856 patients with mild cognitive impairment (mci) due to alzheimer’s disease or mild alzheimer’s dementia (collectively known as early alzheimer’s disease) with confirmed amyloid pathology in the brain. this study used bayesian adaptive randomization design to automatically allocate newly enrolled patients into the study to treatment arms showing higher probability of efficacy based on the results of interim analyses. the study design included five dose regimens and placebo, and considered the efficacy of ban2401 as well as dose responsiveness through 16 interim analyses that assessed potential for early success, an analysis based on adcoms at 12 months, and a comprehensive final analysis at 18 months (secondary endpoints). patients who received treatment with ban2401 were randomized to five dose regimens, 2.5 mg/kg biweekly (52 patients), 5 mg/kg monthly (51 patients), 5 mg/kg biweekly (92 patients), 10 mg/kg monthly (253 patients), or 10 mg/kg biweekly (161 patients). biomarker endpoints included changes in aβ accumulated in the brain as measured by amyloid pet (positron emission tomography) as well as in cerebrospinal fluid (csf), while adcoms (alzheimer’s disease composite score), clinical dementia rating sum of boxes (cdr-sb) and alzheimer’s disease assessment scale-cognitive subscale (adas-cog) were measured as efficacy endpoints (clinical).

detailed results of study 201 were presented at alzheimer’s association international conference 2018 and clinical trials on alzheimer’s disease 2018 in july 2018 and october 2018, respectively.

currently, an open-label extension phase of study 201 is ongoing. eligible patients are those enrolled in study 201, and receive the highest dose of ban2401 (10 mg/kg biweekly).

3. about bioarctic ab
bioarctic ab (publ) is a swedish research-based biopharma company focusing on disease modifying treatments and reliable biomarkers and diagnostics for neurodegenerative diseases, such as alzheimer’s disease and parkinson’s disease. the company also develops a potential treatment for complete spinal cord injury. bioarctic focuses on innovative treatments in areas with high unmet medical needs. the company was founded in 2003 based on innovative research from uppsala university, sweden. collaborations with universities are of great importance to the company together with our strategically important global partners in the alzheimer (eisai) and parkinson (abbvie) projects. the project portfolio is a combination of fully funded projects run in partnership with global pharmaceutical companies and innovative in-house projects with significant market- and out-licensing potential. bioarctic’s b-share is listed on nasdaq stockholm mid cap (sto:bioa b). www.bioarctic.com.

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