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在中国能做BE试验样本分析的公司名录。   [更多]

控制体内血糖水平是成功治疗许多疾病的关键，如糖尿病。 因此， Novo Nordisk公司正在寻找新的小分子，它可以于D-葡萄糖的生理集合密切结合 (持续的取代，Kd，低毫摩尔范围) 悬赏须提交概念性实验数据报告和样品，Novo Nordisk公司将决定最终得奖者，并颁发起始奖金200000美金。 另外Novo Nordisk公司将提议基于里程碑式的合约，如果分子式在未来悬赏中得到成功研发，将会得到二次奖项。 悬赏截止时期2017年1月9日, 投标网址：https://www.innocentive.com/ar/projectRoom/index?challenge=9933823 原文: Novo Nordisk Challenge: Design and Synthesis of a Small Molecule Glucose Binder TAGS: Chemistry, Life Sciences, Royal Society of Chemistry, RTP AWARD: $200,000 USD | DEADLINE: 1/09/17 | ACTIVE SOLVERS: 145 | POSTED: 3/30/16 The control of glucose levels in the body is key for successful treatment of many disease states such as diabetes. Hence, Novo Nordisk is looking for novel small molecules that can bind with affinities matching the physiological concentrations of D-glucose (displacement constant, Kd, in the low millimolar range). This is a Reduction-to-Practice Challenge that requires written documentation, experimental proof-of-concept data, and sample delivery. Additionally, the Challenge has the following unique features.Please read carefully the Challenge-Specific Agreement. • Solvers are asked to prepare the compound and perform binding affinity assays to glucose in aqueous solution under conditions described in the Challenge Description. The compounds must also be supplied to Novo Nordisk in sufficient amounts to reproduce the results. Upon experimental validation of the results, Novo Nordisk will make an award (‘Initial Transfer Fee’) of $200,000 to the best solution as solely determined by the Seeker, according to the Challenge requirements. The Awarded Solver grants Novo Nordisk an exclusive license under the terms described in the Challenge-Specific Agreement. • Additionally, Novo Nordisk will offer a milestone-based agreement to the Solver, establishing the terms of payment of anadditional award (‘Secondary Award’), should the small molecule be successful in its development post-Challenge(‘Second Evaluation Period’), in exchange   [更多]

招募急性痛风性关节炎志愿者 招募概述： 如果您是急性痛风性关节炎患者，符合以下条件就可以报名参加虎贞痛风胶囊的临床研究。虎贞痛风胶囊由广东一力集团制药有限公司/广州暨南生物医药研究开发基地有限公司研制并提供的，并于2008年经国家食品药品监督管理局批准进行临床研究，临床试验批件号：2008L02043。其具有清热利湿，化瘀利浊，滋补肝肾的功效。主治急性痛风性关节炎（湿热蕴结证），症见：关节红肿热痛，伴有发热，汗出不解，口渴喜饮，心烦不安，小便黄及痛风病见上述症候者。此研究由中国中医科学院广安门医院等15家医院共同参与。 如果您愿意参加本项研究并通过筛选符合条件，我们将为您提供3天的免费治疗并免费进行相关检查（包含：体格检查、血常规、尿常规、便常规、肝肾功、心电图、血尿酸、类风湿因子、血沉、C反应蛋白和抗链球菌溶血素‘O’）。 入选条件： 1.符合急性痛风性关节炎诊断标准，且辨证为湿热蕴结证。 2.急性发作在48小时之内，本次发作未用过治疗药（包括秋水仙碱、非甾类抗炎药及激素等）者。 3.VAS评分≥4分。 4.年龄18-65岁。 5.签署知情同意书。 您一旦参加本试验将获得较全面的检查和试验药物治疗，并将得到医生的全面跟踪随访。 如您符合纳入标准，并有意参加本研究项目，请到辽宁中医药大学第二附属医院住院部A楼三楼糖尿病科咨询 。 地址：沈阳市皇姑区黄河北大街60号 联系方式：江红主任：138 4008 4568 马尧医生：139 4046 6290   [更多]

罕见癌症研究基金会(RCRF),致力于通过战略投资和创新合作进行基础治疗罕见的癌症,和美国文化募捐组织(ATCC),世界上最大的非营利性细胞株库,建立神经内分泌肿瘤细胞株收集目录。肠道良性肿瘤和胰腺神经内分泌肿瘤(PNET)需求一种新疗法的研究和发展，即在体内原发性肿瘤中建立新的细胞株。 为了刺激发展新的良性肿瘤和PNET细胞系,该基金会是高兴地宣布第二次开放竞争十个人奖项:开发人员的第一个新的细胞系在每个疾病(肠道良性肿瘤和PNET)将获得100000美元，开发者的第二,第三,第四,第五个新细胞系在每个疾病将会收到50000美元。原文如下：https://www.innocentive.com/ar/challenge/9933756 The lack of well-validated and widely accepted cell lines derived from intestinal carcinoid and pancreatic neuroendocrine tumors (PNET) is a significant barrier for research and development of new therapies. The Caring for Carcinoid Foundation therefore wishes to launch a second Challenge to stimulate a concerted effort to create a “collection” of well-characterized cell lines that faithfully replicate tumor characteristics and genetics. The Foundation has partnered with the Rare Cancer Research Foundation (RCRF), a foundation dedicated to curing rare cancers through strategic investments and innovative collaborations, and the American Type Culture Collection (ATCC), the world’s largest non-profit cell line repository, to establish a Neuroendocrine Tumor Cell Line collection in their catalog. This is a Reduction-to-Practice Challenge that requires written documentation, detailed description of each cell line, and sample delivery. Source: InnoCentive Challenge ID: 9933756 Challenge Overview This Challenge is intended to encourage innovative approaches to establishing new cell lines from primary tumors that grow slowly in vivo and to publicize new methods as well as availability of the new cell lines for broad, unrestricted use. To stimulate development of new carcinoid and PNET cell lines, the Foundation is pleased to announce its second open competition for up to ten individual prizes: Developers of the first new cell lines in each disease (intestinal carcinoid and PNET) will receive $100,000 each and developers of the second, third, fourth, and fifth new cell lines in each disease will receive $50,000 each. Individual   [更多]

肝脏疾病是一种由病毒或有毒物连续侵害造成肝脏晚期纤维化的慢性疾病。目前，我们的治疗方法很有限，寻找治疗方法的大多数临床试验都失败了，部分原因是由于缺乏预测肝脏疾病发展的生物标志物。公司需要寻找一种新的生物标志物，对提高疾病的可控性会有很大的帮助，定期监测生物标志物也可以促进临床试验治疗药物的进一步发展。 具体可以查看https://www.innocentive.com/ar/challenge/9933671 Challenge Overview Liver disease represents a worldwide unmet medical need. Although there are various causes, the danger is that the liver will become so damaged that it can no longer function adequately. Whether the insult is a viral infection, chemical injury, or immune-related, liver disease follows a slow and steady progression. Early stage liver disease is characterized by inflammation, which if left untreated, can cause scarring and fibrosis. A healthy liver is capable of repair and regeneration, but when there are architectural changes to the tissue, the damage can no longer be reversed. Biopsies are routinely conducted to diagnose liver fibrosis and cirrhosis. Undergoing this invasive procedure involves significant abdominal pain along with the risk for complications and sampling error. Therefore, many patients are reluctant to have a second biopsy even when it is medically advisable. The Seeker desires a specific and sensitive biomarker(s) that is highly associated with liver fibrosis and could be used as a surrogate for clinical efficacy and ideally, could guide treatment selection. Submissions to this Challenge must be received by 11:59 PM (US Eastern Time) on August 17, 2015. Late submissions will not be considered. This is a Theoretical Challenge that requires only a written proposal to be submitted. The Challenge award will be contingent upon theoretical evaluation of the proposal by the Seeker. To receive an award, Solvers will not be required to transfer their exclusive IP rights to the Seeker. Instead, as further described in the Challenge-Specific Agreement, Solvers will grant to the Seeker a one hundred and eighty (180)-day Exclusivity Period from the deadline [11:59 PM (US Eastern Time) on August 17, 2015] for a non-exclusive   [更多]

不能控制其发作的癫痫猝死（SUDEP）是导致年轻人死亡的主要原因。每年超过千分之一的癫痫患者死于猝死，如果是不受控制的癫痫发作，风险会增加一百五十分之一。一种普遍恐惧的意识和持续受到的歧视导致太多的人隐藏自己的癫痫病情而没有接受持续治疗或寻求更有效的治疗方法。这增加了他们癫痫猝死的风险 癫痫基金会帮助机构决心改变这种状况，开展一个创意的宣传活动，鼓励人们寻求最佳的癫痫发作和癫痫发作控制和教育他们自己和他们的家庭以及他们如何可以减轻癫痫猝死的风险。此外，这个活动应该邀请更广泛的医疗保健社区讨论SUDEP，明白不接受持续发作的重要性，并寻找一种更有效的治疗方法。具体（https://www.innocentive.com/ar/challenge/9933717）如下 TAGS: Global Health, Business/Entrepreneurship, Life Sciences, Scientific American, Ideation AWARD: $15,000 USD | DEADLINE: 7/13/15 | ACTIVE SOLVERS: 12 | POSTED: 6/09/15 Sudden unexpected death in epilepsy (SUDEP) is the leading cause of death in young adults who have epilepsy and cannot control their seizures. Each year, more than 1 out of 1,000 people with epilepsy die from SUDEP, and, if seizures are uncontrolled, the risk increases to more than 1 out of 150. A widespread lack of awareness and ongoing fear and discrimination lead too many individuals to hide their epilepsy and to accept ongoing seizures instead of seeking out more effective treatments. This increases their risk of SUDEP. The Epilepsy Foundation SUDEP Institute is determined to change this and is challenging Solvers to come up with ideas for a creative advocacy campaign that encourages people with seizures and epilepsy to seek optimal seizure control and to educate themselves and their families about SUDEP and how they can mitigate its risks. In addition, the campaign should invite the broader health care community to talk about SUDEP, understand the importance of not accepting ongoing seizures, and pursue all effective treatment options. Can you help us to demystify seizures and epilepsy, and empower people with epilepsy? This is an Ideation Challenge with a guaranteed award for at least one submitted solution.   [更多]

我们体内以分泌胰岛素来维持胰岛细胞血糖水平和体内平衡。而糖尿病患者的胰岛细胞是缺乏或无效的。没有足够活性的胰岛素，糖尿病患者就无法控制血糖。胰岛移植是一种治疗策略,糖尿病患者需要胰岛素注射来控制他们的疾病，减轻或根除症状。阿斯利康正在寻找一个简单的装置将人类胰岛移植出来，来检测药物的性能。 具体如下网站，https://www.innocentive.com/ar/challenge/9933735 Pancreatic islet beta-cells sense blood sugar levels and secrete insulin to maintain homeostasis. In patients with diabetes, islet beta-cells are either lacking or ineffective. Islet transplantation is a treatment strategy that allows diabetics to reduce or eliminate the need for insulin injections to control their disease. AstraZeneca is searching for a simple device to transplant human islets to facilitate testing of therapeutic agents. This Challenge requires only a written proposal. Source: InnoCentive Challenge ID: 9933735 Challenge Overview Diabetes is a disease of the pancreatic islet cells. Of the four cell types, insulin-producing beta-cells are the most abundant. Without adequate levels of insulin, diabetes patients have difficulty controlling their blood sugar. One alternative to self-administration of medicine is islet transplantation. The procedure involves an infusion of isolated donor islets into the patient. If the graft is accepted, these islets will function to regulate blood glucose levels through the production of insulin. AstraZeneca is searching for a simple device for the transplantation and subsequent retrieval of human islets to support in vivo testing of therapeutic agents. ABOUT THE SEEKER AstraZeneca is a global, research-based, biopharmaceutical company with a focus on five key therapeutic areas: 1) cardiovascular & metabolic diseases, 2) oncology, 3) respiratory, inflammation & autoimmunity, 4) neuroscience, and 5) infection. As an innovation-driven, research organization, AstraZeneca recognizes that great ideas come from many sources. Open innovation is an avenue by which ideas can be shared and AstraZeneca recently launched a pavilion to further its commitment to facilitate the advancement of pharmaceutical   [更多]

弥漫性大B细胞淋巴瘤(DLBCL)是一种最常见的非霍奇金淋巴瘤，诊断病例在美国约占淋巴瘤的30%。它是一种特异质性疾病。由于临床多样性和复杂性,又有新的突变在某些难治性患者身上被发现。阿斯利康需要创建一种弥漫性巨大B细胞淋巴瘤的合适的临床模型。 具体链接在：https://www.innocentive.com/ar/challenge/9933016 AstraZeneca Challenge: Developing Clinically-Relevant Models for Diffuse Large B Cell Lymphoma (DLCBL) TAGS: AstraZeneca, Physical Sciences, Life Sciences, Nature, Requests for Partners and Suppliers, Chemistry, RTP AWARD: See details | DEADLINE: 6/02/15 | ACTIVE SOLVERS: 9 | POSTED: 3/04/15 Diffuse large B cell lymphoma (DLBCL) is the most common form of non-Hodgkin lymphoma and accounts for up to 30% of newly diagnosed cases in the United States. It is a heterogeneous disease which in part appears to be driven by chronic activation of key survival pathways. A limited number of DLBCL cell lines are available, however there are gaps, and specific patient subtypes are not represented. To add to the complexity of clinical diversity, new mutations are being identified in certain treatment-resistant patients. AstraZeneca is interested in innovative proposals to create suitable preclinical models of DLBCL. This is a Reduction-to-Practice Challenge that requires a written proposal and experimental proof-of-concept data (and/or sample delivery). The Challenge has a special award structure. Whether creating a model for DLBCL or a model of acquired resistance to ibrutinib, up to $10,000 will be designated for solutions that highlight novel technologies to generate in vitro cell lines, whereas up to $25,000 will be awarded for submissions that successfully utilize patient-derived tissues.   [更多]

【基本信息】 需要 受试者类型 ： 健康受试者 性 别 ： 女性 婚 姻 状 况 ： 不限 适 应 专 业 ： 药物适应症： 抗菌 招 募 人 数： 200人 试验起止日期 ： 2015-02-27 -- 2016-03-24 报名截止日期 ： 2015-03-23 补 偿 金 ： ￥3000 【项目描述】 一项西他沙星的临床实验 【入选标准】 18到45岁，身体健康， 【排除标准】 【研究中心列表】 南京 江苏省人民医院 【联系方式】 联系人 ： 陈凯 手 机 ： 13115295869   [更多]

需要受试者类型 ： 健康受试者 性别 ： 不限 婚 姻 状 况 ： 不限 适 应 专 业 ： 药物适应症： 抗菌 招 募 人 数： 20人 试验起止日期 ： 2015-03-07 -- 2015-04-30 报名截止日期 ： 2015-03-30 补 偿 金 ： ￥3700 【项目描述】 需要服用盐酸头孢替安酯一天三次或两次，连续服用5天，需要采血34次，每次4ml，共136ml（其中第一天和第五天采血各采血16次，第3、4天晨起采血一次）。 【入选标准】 1、健康成年男性或女性，年龄在18～40岁范围内； 2、体重指数(BMI)=体重kg/[(身高m)×(身高m)]，在19～24范围内； 【排除标准】 1、三年内有胃肠道疾病史（含现有）者，包括慢性或活动性上消化道疾病如吞咽困难、食管疾病、胃炎、十二指肠炎、溃疡，消化道溃疡或活动性胃肠道出血或消化道手术者； 2、有精神病史、药物滥用史或躯体残疾； 3、处于妊娠或哺乳期，或未采取一种或一种以上避孕措施等导致不能确保在试验前2周至试验后三个月不受孕的女性； 4、入选前3个月内参加过其它临床试验； 5、经体格检查各项体检指标有发现异常（经临床医师判断有临床意义）； 6、根据研究者的判断，具有较低入组可能性（如体弱等）； 7、过敏体质，如已知对两种或以上物质过敏史者；或已知对本药品组分或其它抗生素类药物有既往过敏史者； 8、父母、兄弟中，具有易引发支气管喘息、出疹、荨麻疹等过敏症状体质者； 9、试验前2周内服用任何中西药； 10、试验前1个月内有献血行为； 11、每周喝酒超过28单位酒精（1单位=285 ml啤酒、或25 ml 超过40度的烈酒、或1高脚玻璃杯葡萄酒）； 12、每天吸烟超过10支或等量的烟草。 【研究中心列表】 广州 广东省人民医院 【联系方式】 联系人 ： 麦医生 手 机 ： 18664116784   [更多]