Tramadol Hydrochloride

- Enrollment completed in Phase 1b/2a clinical trial of AJ201 for spinal and bulbar muscular atrophy; topline data expected in second quarter of 2024 - - Presented positive BAER-101 preclinical data at American Epilepsy Society (AES) and American Society for Experimental Neurotherapeutics (ASENT) Annual Meetings and in publication Drug Development Research - - Final agreement reached with FDA on study design and analysis approach for Phase 3 safety study of IV tramadol – MIAMI, March 18, 2024 (GLOBE NEWSWIRE) -- Avenue Therapeutics, Inc. (Nasdaq: ATXI) (“Avenue” or the “Company”), a specialty pharmaceutical company focused on the development and commercialization of therapies for the treatment of neurologic diseases, today reported financial results and recent corporate highlights for the year ended December 31, 2023. “We made considerable progress across our pipeline of differentiated neurologic therapies in 2023," said Alexandra MacLean, M.D., Chief Executive Officer of Avenue. “Avenue demonstrated tremendous execution capabilities with our lead clinical program AJ201, a potential first-in-class treatment for spinal and bulbar muscular atrophy (SBMA), also known as Kennedy’s Disease. Within nine months of acquiring the rights to AJ201 in March 2023, we dosed the first patient in the Phase 1b/2a clinical trial, and we completed trial enrollment of 25 SBMA patients across six sites in the U.S. We remain on track to report topline data for AJ201 in the second quarter of 2024, an incredibly exciting milestone for both the Company and patients suffering from SBMA, a debilitating rare neuromuscular disorder with no approved treatments in the U.S. Additionally, we have progressed BAER-101 for the treatment of epilepsy by presenting preclinical data from a translational animal model in multiple peer-reviewed forums. We have also advanced IV tramadol, reaching final agreement with the U.S. Food and Drug Administration (FDA) on the safety study and statistical analysis approach for the final Phase 3 study. Pending additional financing, we look forward to progressing BAER-101 and IV tramadol for patients facing great unmet need. We look forward to another productive year in 2024 as we continue to make significant strides across our clinical pipeline and advance our mission of providing impactful therapies to patients suffering from neurologic diseases.” Recent Corporate Highlights: AJ201 (Nrf1 and Nrf2 activator, androgen receptor degradation enhancer for SBMA) In January 2024, Avenue completed enrollment in the Phase 1b/2a clinical trial of AJ201 for the treatment of SBMA. The 12-week, multicenter, randomized, double-blind Phase 1b/2a clinical trial of AJ201 enrolled 25 patients randomly assigned to AJ201 (600 mg/day) or placebo. The primary endpoint of the study is to assess safety and tolerability of AJ201 in subjects with clinically and genetically defined SBMA. Topline data for the Phase 1b/2a study are anticipated in the second quarter of 2024. More information about this study can be found at ClinicalTrials.gov (Identifier: NCT05517603). BAER-101 (GABAA α2/3 positive allosteric modulator) Avenue presented preclinical results for BAER-101, a potentially best-in-class selective GABAA α2,3 positive allosteric modulator, in three scientific peer-reviewed settings, including the American Epilepsy Society (AES) Annual Meeting in December 2023, the publication Drug Development Research in February 2024 and the American Society for Experimental Neurotherapeutics (ASENT) Annual Meeting in March 2024. The in vivo data showcase BAER-101’s ability to significantly suppress seizures using the SynapCell’s Genetic Absence Epilepsy Rat from Strasbourg (“GAERS”) model of epilepsy. BAER-101 fully suppressed seizure activity in the GAERS model with a minimal effective dose of 0.3 mg/kg, PO, and the effect was fast in onset and stable throughout the duration of testing. The data also demonstrated BAER-101’s ability to selectively target GABAA α2 and α3 subtypes more than α1 and α5, potentially improving anti-convulsant and anxiolytic activity while minimizing the risk of tolerance and abuse associated with existing treatments in this drug class. Subject to obtaining the necessary financing, which could be provided through a strategic partnership, Avenue plans to initiate a Phase 2a clinical trial of BAER-101 to further study its anti-seizure properties in patients with common or rare epilepsies. IV Tramadol In January 2024, Avenue reached final agreement with the FDA on the safety study protocol and statistical analysis approach for the Phase 3 study for intravenous (“IV”) tramadol, which is in development for the treatment of acute post-operative pain in a medically supervised setting. The final non-inferiority study is designed to assess the theoretical risk of opioid-induced respiratory depression related to opioid stacking on IV tramadol compared to IV morphine. The study will randomize approximately 300 post bunionectomy patients to IV tramadol or IV morphine for pain relief administered during a 48-hour post-operative period. Patients will have access to IV hydromorphone, a Schedule II opioid, for rescue of breakthrough pain. Pending additional financing, Avenue aims to initiate the Phase 3 safety study as soon as feasible. The Company believes that the study can be completed and submitted to the FDA within 12 months of the study’s initiation. General Corporate In March 2024, Avenue announced that the Nasdaq Hearings Panel granted the Company’s request for an extension to evidence compliance with all applicable criteria for continued listing on The Nasdaq Capital Market, including the $1.00 bid price and $2.5 million stockholders’ equity requirements, through May 20, 2024. 2023 Financial Results: Cash Position: As of December 31, 2023, cash and cash equivalents totaled $1.8 million, compared to $6.7 million at December 31, 2022, a decrease of $4.9 million. In January 2024, the Company completed a warrant inducement transaction resulting in $5.0 million in gross proceeds.R&D Expenses: Research and development expenses for the full year 2023 were $6.1 million, compared to $2.7 million in 2022. Additionally, there was $4.2 million in expense for the acquisition of the AJ201 license in 2023.G&A Expenses: General and administrative expenses for the full year 2023 were $4.2 million, compared to $5.3 million in 2022.Net Loss: Net loss for the full year 2023 was $10.5 million, or $0.98 per share, compared to a net loss of $3.6 million, or $1.63 per share, in 2022. About Avenue TherapeuticsAvenue Therapeutics, Inc. (Nasdaq: ATXI) is a specialty pharmaceutical company focused on the development and commercialization of therapies for the treatment of neurologic diseases. It is currently developing three assets including AJ201, a first-in-class asset for spinal and bulbar muscular atrophy, BAER-101, an oral small molecule selective GABAA α2, α3 receptor positive allosteric modulator for CNS diseases, and IV tramadol, which is in Phase 3 clinical development for the management of acute postoperative pain in adults in a medically supervised healthcare setting. Avenue is headquartered in Miami, FL and was founded by Fortress Biotech, Inc. (Nasdaq: FBIO). For more information, visit www.avenuetx.com. Forward-Looking StatementsThis press release contains predictive or “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. All statements other than statements of current or historical fact contained in this press release, including statements that express our intentions, plans, objectives, beliefs, expectations, strategies, predictions or any other statements relating to our future activities or other future events or conditions are forward-looking statements. The words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “predict,” “project,” “will,” “should,” “would” and similar expressions are intended to identify forward-looking statements. These statements are based on current expectations, estimates and projections made by management about our business, our industry and other conditions affecting our financial condition, results of operations or business prospects. These statements are not guarantees of future performance and involve risks, uncertainties and assumptions that are difficult to predict. Therefore, actual outcomes and results may differ materially from what is expressed or forecasted in, or implied by, the forward-looking statements due to numerous risks and uncertainties. Factors that could cause such outcomes and results to differ include, but are not limited to, risks and uncertainties arising from: the fact that we currently have no drug products for sale and that our success is dependent on our product candidates receiving regulatory approval and being successfully commercialized; the possibility that serious adverse or unacceptable side effects are identified during the development of our current or future product candidates, such that we would need to abandon or limit development of some of our product candidates; our ability to successfully develop, partner, or commercialize any of our current or future product candidates including AJ201, IV tramadol, and BAER-101; the substantial doubt raised about our ability to continue as a going concern, which may hinder our ability to obtain future financing; the significant losses we have incurred since inception and our expectation that we will continue to incur losses for the foreseeable future; our need for substantial additional funding, which may not be available to us on acceptable terms, or at all, which unavailability of could force us to delay, reduce or eliminate our product development programs or commercialization efforts; our reliance on third parties for several aspects of our operations; our reliance on clinical data and results obtained by third parties that could ultimately prove to be inaccurate, or unreliable, or unacceptable to regulatory authorities; the possibility that we may not receive regulatory approval for any or all of our product candidates, or that such approval may be significantly delayed due to scientific or regulatory reasons; the fact that even if one or more of our product candidates receives regulatory approval, they will remain subject to substantial regulatory scrutiny; the effects of current and future laws and regulations relating to fraud and abuse, false claims, transparency, health information privacy and security, and other healthcare laws and regulations; the effects of competition for our product candidates and the potential for new products to emerge that provide different or better therapeutic alternatives for our targeted indications; the possibility that the government or third-party payors fail to provide adequate coverage and payment rates for our product candidates or any future products; our ability to establish sales and marketing capabilities or to enter into agreements with third parties to market and sell our product candidates; our exposure to potential product liability claims; related to the protection of our intellectual property and our potential inability to maintain sufficient patent protection for our technology and products; our ability to maintain compliance with the obligations under our intellectual property licenses and funding arrangements with third parties, without which licenses and arrangements we could lose rights that are important to our business; the fact that Fortress Biotech, Inc. controls a majority of the voting power of our outstanding capital stock and has rights to receive significant share grants annually;; and those risks discussed in our filings which we make with the SEC. Any forward-looking statements speak only as of the date on which they are made, and we undertake no obligation to publicly update or revise any forward-looking statements to reflect events or circumstances that may arise after the date of this press release, except as required by applicable law. Investors should evaluate any statements made by us in light of these important factors. Contact: Jaclyn JaffeAvenue Therapeutics, Inc. (781) 652-4500ir@avenuetx.com AVENUE THERAPEUTICS, INC.Consolidated Balance Sheets($ in thousands, except for share and per share amounts) December 31, December 31, 2023 2022 ASSETS Current assets: Cash and cash equivalents$1,783 $6,708 Prepaid expenses and other current assets 67 137 Total assets$1,850 $6,845 LIABILITIES AND STOCKHOLDERS’ EQUITY Current liabilities: Accounts payable and accrued expenses$287 $949 Accounts payable and accrued expenses - related party 323 21 Warrant liability 586 2,609 Total current liabilities 1,196 3,579 Total liabilities 1,196 3,579 Commitments and Contingencies Stockholders’ equity Preferred stock ($0.0001 par value), 2,000,000 shares authorized Class A Preferred stock, 250,000 shares issued and outstanding as of December 31, 2023 and 2022, respectively — — Common stock ($0.0001 par value) Common shares, 75,000,000 shares authorized and 25,597,622 shares issued and outstanding as of December 31, 2023; and 20,000,000 shares authorized and 4,773,841 shares issued and outstanding as of December 31, 2022 3 — Additional paid-in capital 92,507 84,456 Accumulated deficit (90,928) (80,551)Total stockholders’ equity attributed to the Company 1,582 3,905 Non-controlling interests (928) (639)Total stockholders’ equity 654 3,266 Total liabilities and stockholders’ equity$1,850 $6,845 AVENUE THERAPEUTICS, INC.Consolidated Statements of Operations($ in thousands, except for share and per share amounts) For the Years Ended December 31, December 31, 2023 2022 Operating expenses Research and development$6,131 $2,698 Research and development - licenses acquired 4,230 — General and administrative 4,179 5,345 Loss from operations (14,540) (8,043) Interest income (126) (20)Financing costs – warrant liabilities 332 1,160 Change in fair value of warrant liabilities (4,258) (5,580)Net loss$(10,488) $(3,603) Net loss attributable to non-controlling interests (111) (51)Net loss attributable to common stockholders$(10,377) $(3,552) Net loss per common share attributable to common stockholders, basic and diluted$(0.98) $(1.63) Weighted average number of common shares outstanding, basic and diluted 10,591,636 2,185,159

☝ 点击上方 一键预约 ☝   最新最热的医药健康新闻政策20240317药品高端会员区HOT高端会员1【会员编号】y1172【所在地区】北京，河北，山西【所在公司】黑龙江久久药业有限责任公司【工作职务】河北山西招商经理【相关产品】 ①【香砂养胃颗粒】基药，独家无蔗糖，国家专利保护剩余19年，医保甲，OTC乙。②【刺五加颗粒】独家剂型无蔗糖，医保乙，OTC甲。③【小儿清热止咳口服液】妇儿急抢目录，医保乙，OTC甲。④【健儿消食口服液】基药，医保乙，OTC甲。【自身资源】基独家，基药【需要资源】河北，山西三终端，或临床代理高端会员2【会员编号】y1199【所在地区】吉林省【所在公司】长春海悦药业有限公司【工作职务】省区经理【相关产品】海悦美奥，悦思立普，伏立康唑，丙戊酸钠注射用浓溶液，他达拉非，注射用阿奇霉素（儿童），曲克芦丁，盐酸氨溴索，盐酸美金刚等【自身资源】吉林省内分泌专家以及医院资源，商业公司合作资源（大商业以及地方商业）；吉林省慢病产品市场布局及推广策略（策略层面）【需要资源】吉林省及东北三省的准入资源，消化内科准入以及一线客户资源（多方式合作）；阿奇霉素注射液市场分析报告（成人&儿童）、奥美拉唑市场分析报告高端会员3【会员编号】y1211【所在地区】陕西【所在公司】北京轩竹生物科技有限公司【工作职务】省区经理【相关产品】安奈拉唑钠【自身资源】政府事务（医保局）  核心医院ICU临床【需要资源】医院准入 药剂关系 代理商高端会员4【会员编号】y1198【所在地区】川渝藏【所在公司】江西青峰药业有限公司【工作职务】省区经理【相关产品】艾司奥美拉唑镁肠溶片、枸橼酸托法替布片、阿哌沙班片、富马酸丙酚替诺福韦片、恩替卡韦分散片/胶囊、盐酸乌拉地尔注射液、阿普米司特片、雷贝拉唑钠肠溶片、枳实总黄酮片。【自身资源】政府事务，四川省消化专家以及医院资源，商业公司合作资源【需要资源】一线客户资源和代理商资源高端会员5【会员编号】y1087【所在地区】湖南【所在公司】清华德仁西安幸福制药有限公司【工作职务】大区经理【相关产品】生血宝合剂、五灵胶囊、热炎宁合剂、童康颗粒【自身资源】厂家产品资源【需要资源】临床类型代理商：湖南省级代理商；湖南省地区代理商。高端会员6【会员编号】y0134【所在地区】北京【所在公司】北京杏林知松科技有限公司【工作职务】销售总监【相关产品】环磷腺苷葡胺、益心胶囊、盐酸曲马多分散片【自身资源】北京临床渠道多年、全国总代产品【需要资源】各省总代资源、厂家资源高端会员7【会员编号】y1150【所在地区】贵州【所在公司】贵州佳德同汇健康咨询服务有限公司【工作职务】业务负责人【相关产品】安奈拉唑钠肠溶片、头孢呋辛钠氯化钠注射液、甘草酸单铵半胱氨酸氯化钠注射液等三十几个产品【自身资源】贵州省代。贵州部分医院资源，产品资源。【需要资源】有医院资源的客户，需具备开发能力。可提供品种和资金。高端会员8【会员编号】y0855【所在地区】北京【所在公司】北京伟林恒昌医药科技有限公司【工作职务】总经理【相关产品】自己持有:阿托伐他汀钙片，奥洛他定片【自身资源】招商和对外贴牌生产【需要资源】需要各省OTC销售团队高端会员9【会员编号】y1002【所在地区】北京 【所在公司】国药控股北京有限公司【工作职务】采购中心市场部经理【相关产品】药品、器械等【自身资源】北京招采信息【需要资源】全国招采信息高端会员10【会员编号】y1142【所在地区】江苏南京 【所在公司】凡森特医药【工作职务】销售总监【相关产品】抗生素/化药/器械/中成药【自身资源】渠道、产品、学术【需要资源】客户、渠道高端会员11【会员编号】y1193【所在地区】北京【所在公司】北京康辰生物【工作职务】法务合规经理【相关产品】原研药品-骨松骨痛相关【自身资源】药械合规及法律相关【需要资源】关于医药行业的合规及法律相关的信息高端会员12【会员编号】y0317【所在地区】湖南长沙【所在公司】湖南广药恒生医药有限公司【工作职务】采购总监【相关产品】一类麻精产品【自身资源】广药集团国企、有一类麻精配送资质、全省医疗机构覆盖配送、新品开发进院能力较强、招商产品可协助推广。【需要资源】医院自营产品、零售分销业务全省配送。高端会员13【会员编号】y1128【所在地区】云南省昭通市【所在公司】云南蓝蝶医疗器械有限公司【工作职务】总经理【相关产品】医疗产品【自身资源】昭通市及昭通周边地区的客户资源【需要资源】优质的医疗产品，及其他地州的客户资源高端会员14【会员编号】y1226【所在地区】四川成都 【所在公司】四川启源药业有限公司【工作职务】总监【相关产品】医保甲类基药【自身资源】厂家临床基药医保产品【需要资源】江西省区临床团队及省第三终端资源高端会员15【会员编号】y1187【所在地区】南京【所在公司】悦康药业【工作职务】招商经理【相关产品】活心丸【自身资源】基药，甲类，安全性高【需要资源】江苏地区招商高端会员16【会员编号】y1116【所在地区】福建（主战区）江西、浙江、江苏【所在公司】康美药业股份有限公司【工作职务】区域经理【相关产品】厂家直销，包含中药饮片、燕窝虫草等贵系礼品【自身资源】1.国家膏方丸剂代煎等试点单位以及集采中标单位之一；2.可自产600多个品种上万个品规；3.可根据医院要求定制高标及小包装饮片；4.药剂科资源【需要资源】1、福建、江西、浙江、江苏区域的代理商；2、各大医院及中医馆高层资源高端会员17【会员编号】y1140【所在地区】北京【所在公司】吉林天衡药业有限公司【工作职务】市场运营部部长【相关产品】铝碳酸镁咀嚼片、瑞舒伐他汀钙片、秋水仙碱片【自身资源】可合作CRO、CMO、CDMO【需要资源】销售代理商；寻找生产场地：片剂，适应症为痛风，特点是该原料为细胞毒药物，寻求细胞毒专线或可与细胞毒药物共线的生产场地。高端会员18【会员编号】y0584【所在地区】天津【所在公司】天津市医药集团泰宁医药【工作职务】市场总监【相关产品】狗皮膏、护肝胶囊、更年安胶囊、连翘败毒片、葡萄糖酸钙片等基药品种，全国多个省和直辖市已中标【自身资源】熟悉国各省招投标政府事务，有成熟的全国销售网络【需要资源】急需各省和直辖市的临床团队高端会员19【会员编号】y0907【所在地区】北京、天津【所在公司】海诚医药集团有限公司【工作职务】省区经理【相关产品】肌苷注射液（静注）、龙血竭胶囊（肠溶）、强力枇杷露（炼蜜）、磷酸川芎嗪注射液（供静脉注射用）、注射用伏立康唑、甘油灌肠剂、注射用哌拉西林钠、注射用头孢唑肟钠、注射用头孢哌酮钠舒巴坦钠、注射用氨苄西林钠舒巴坦钠、曲克芦丁注射液、核黄素磷酸钠注射液、注射用尼麦角林等产品【自身资源】全国总代理产品资源【需要资源】寻临床代理商、省总、地总团队合作高端会员20【会员编号】y1219【所在地区】内蒙古【所在公司】源浩医疗【工作职务】总经理【相关产品】处方药【自身资源】整个乌兰察布市二级医院、卫生院、诊所资源【需要资源】独家基药、集采品种、OTC控销产品厂家资源高端会员21【会员编号】y0947【所在地区】江西南昌【所在公司】江西金耐康医药科技有限公司【工作职务】经理【相关产品】神外、妇产、肿瘤领域产品【自身资源】福建和江西省代和医院客户资源，江西神经外科及妇产科专家资源【需要资源】厂家岗位或产品高端会员22【会员编号】y1197【所在地区】辽宁【所在公司】辽宁好护士集团医药有限公司【工作职务】省区经理【相关产品】肾炎温阳片、肾炎解热片【自身资源】独家，挂网，空间好【需要资源】操作肾病产品的医院资源团队高端会员23【会员编号】y1096【所在地区】河南【所在公司】浙江仙琚制药【工作职务】招商大区【相关产品】屈螺酮炔雌醇片（||）【自身资源】河南、河北、江西、安徽、北京、天津等地重点医院客户资源【需要资源】河南、河北、江西、安徽、北京、天津等地妇科团队资源高端会员24【会员编号】y1264【所在地区】枣庄市【所在公司】某医药公司【工作职务】经理【相关产品】肿瘤药【自身资源】等级医院客户【需要资源】最新化药产品资源高端会员25【会员编号】y0321【所在地区】厦门、上海【所在公司】承葛医药集团【工作职务】项目经理【相关产品】微生态移植及相关产业【自身资源】微生态检测、移植、微生态口服产品、微生态研发【需要资源】各类医药资源高端会员26【会员编号】y1221【所在地区】广东【所在公司】陕西盘龙药业集团【工作职务】省区经理【相关产品】1、盘龙七片（骨科）全国独家专利产品、医保甲类无后缀。2、骨松宝片（预防更年期骨质疏松症）。3、克比热提片（独家口服，皮肤科）4、复方醋酸绵酚片（妇科)【自身资源】独家、商业公司合作资源【需要资源】医院准入、广东临床类型代理商高端会员27【会员编号】y1278【所在地区】陕西【所在公司】西安典茂轩医药科技【工作职务】总经理【相关产品】雾化全系列，抗生素、心脑血管领域产品。【自身资源】陕西省招商全渠道和连锁OTC自营团队及政务商业资源【需要资源】集采药，国谈化药，进口化药高端会员28【会员编号】y1114【所在地区】四川/西藏【所在公司】浙江孚诺/浙江惠迪森【工作职务】市场/销售主管【相关产品】复方多黏菌素B软膏/注射用拉氧头孢钠【自身资源】1.四川省皮肤科、烧伤科、肛肠科深耕细作10年建立上层专家资源，临床一线专人覆盖，自建团队，高效专业；2.四川、西藏都有自己的分销渠道，西藏有自己的商业配送公司，承接全国产品。【需要资源】1.寻找相关科室品种，签总代、有潜力的专科品种；2.寻找省内手术科室合作伙伴，推广外用抗生素品种在四川的销售。高端会员29【会员编号】y1294【所在地区】浙江【所在公司】浙江天啬生物医药有限公司 、杭州端本医院科技有限公司【工作职务】招商经理【相关产品】主营产品线：骨科，麻醉科，消化科；自有持证：氟比洛芬凝胶贴膏【自身资源】1、浙江省临床品种推广网络;2、自有批文【需要资源】1、全国省级代理合作伙伴；2、浙江省代理推广甲方产品高端会员30【会员编号】y1312【所在地区】重庆【所在公司】重庆旭达药业【工作职务】总经理【相关产品】补肾健脾口服液、食积口服液【自身资源】产品资源、团队资源【需要资源】产品品牌输出高端会员31【会员编号】y0857【所在地区】河北【所在公司】京津医学【工作职务】产品经理【相关产品】养心定悸颗粒 【自身资源】医学实验与研究，团队目前主要承接上市后医学临床再评价项目；临床推广，团队覆盖全国等级医疗及基层医疗招商，京津冀地区临床推广自营【需要资源】全国总代产品，最好是医保或者独家高端会员32【会员编号】y0990【所在地区】新疆【所在公司】新疆迈达医药有限公司【工作职务】销售总监【相关产品】OTC，临床基药产品 【自身资源】具有完善的新疆省临床基药销售渠道和OTC销售渠道【需要资源】新特药，基药产品，集采产品，皮肤科基药产品需要在新疆推广的上游企业可接洽，以及OTC优秀品种，新疆市场可跨渠道运营器械高端会员区高端会员1【会员编号】X0031【所在地区】贵州贵阳【所在公司】贵州众鑫源科技有限公司【工作职务】总经理【相关产品】口腔辅料【自身资源】省级公立医院客户资源【需要资源】耗材，试剂，医美，口腔高端会员2【会员编号】X0028【所在地区】北京【所在公司】北博(北京)医疗器械有限公司【工作职务】总经理【相关产品】电热针治疗仪+耗材内热式电热针灸针【自身资源】有源医疗器械的研发、注册、代工【需要资源】诚招各省耗材代理商,有医保资源,本产品在《全国医疗服务项目技术规范(2023年版)》,需要增加或修订各省医保目录高端会员3【会员编号】X0035【所在地区】云南省昭通市【所在公司】云南蓝蝶医疗器械有限公司【工作职务】销售总监【相关产品】医疗器械相关产品【自身资源】云南省昭通市及昭通周边地区的客情资源【需要资源】优质的产品高端会员4【会员编号】X0045【所在地区】福建【所在公司】福州市东瑞医疗科技有限公司【工作职务】总经理【相关产品】狂免、破免、纤原，人用狂犬疫苗等【自身资源】福建省代，临床医学背景，部分医院、卫健及疾控部门资源【需要资源】适合急诊外科相关药品，耗材产品资源超级高端会员区超级会员1【会员编号】w0201 【所在地区】湖南【所在公司】湖南健朗药业有限责任公司【工作职务】总经理【相关产品】自身持有奥拉西坦胶囊、奥拉西坦注射液、泮托拉唑肠溶胶囊、羟甲烟胺片等产品。【自身资源】招商和对外贴牌生产【需要资源】需要购买若干化学药品注册批文，已出批文或者即将申报的均可。超级会员2【会员编号】w0045【所在地区】山东东营【所在公司】山东凤凰制药股份有限公司【工作职务】普药事业部总监【相关产品】盐酸二甲双胍缓释片、苯磺酸氨氯地平片、辛伐他汀片、维格列汀片、护肝片、降脂宁片、复方丹参片、胃灵颗粒、半夏露颗粒、益母草颗粒、板蓝根颗粒、微达康颗粒、感冒清热颗粒、小儿咽扁颗粒、小儿咳喘灵颗粒、灵芝胶囊、活力胶囊、穿心莲胶囊、黄柏胶囊等【自身资源】厂家产品资源【需要资源】市县级临床业务团队超级会员3【会员编号】w0150【所在地区】山东【所在公司】山东天元盈康医疗科技有限公司【工作职务】销售总监【相关产品】人血白蛋白，破免，狂免，静丙，小儿复方氨基酸注射液，盐酸纳美芬，环磷腺苷 等产品。【自身资源】政府事务 在山东做省代17年 有直营团队 同时通过招商团队覆盖全省医院。【需要资源】上游厂家，国代，批文持有人，原料药超级会员4【会员编号】w0033【所在地区】四川成都 【所在公司】四川省百草生物药业有限公司【工作职务】市场总监【相关产品】苯磺酸氨氯地平片、盐酸舍曲林胶囊、泛昔洛韦片【自身资源】通过一致性评价产品。医保甲类。基药。大部分省份已挂网。渠道终端市场管理好。【需要资源】临床、终端渠道代理商超级会员5【会员编号】w0186【所在地区】山东【所在公司】深圳万和制药有限公司【工作职务】销售部经理【相关产品】商品名：和安，和爽，和流，爱伦多等【自身资源】消化，肝病以及普外等领域专家资源【需要资源】政府事务相关超级会员6【会员编号】w0163【所在地区】广西 【所在公司】广西炬邦乾承投资有限公司【工作职务】总经理【相关产品】集采中选:哌他，左氨氯地平，左卡尼汀，噻肟，呋塞米，他啶，曲松，丙戊酸钠，头孢地尼 呼吸:沙丁，氟替卡松，异丙，左沙，乙酰半胱氨酸，茶碱，孟鲁司特。肾内:左卡，达肝，司维拉姆，促红，百令片。围手术期:羟考酮，纳布啡。布托啡诺。抗感染:磷霉素，哌舒，唑肟，阿奇。慢病:达格列净，格列齐特，氟伐他汀，左氨氯地平，门冬氨氯地平。心脑血管:辅酶Q10，倍他司汀，曲克芦丁，吡拉西坦，己酮可可碱。【自身资源】地方政府事务，专业推广能力，经销商储备，行业口碑认可。【需要资源】甲方产品超级会员7【会员编号】w0160【所在地区】内蒙古 【所在公司】商贸公司【工作职务】总经理【相关产品】集采药品、集采器械、化妆品、特医食品等。【自身资源】35人销售团队【需要资源】集采药品、集采器械、化妆品、特医食品等。超级会员8【会员编号】w0104【所在地区】南京【所在公司】翎耀生物科技（上海）有限公司【工作职务】全国商务分销总监【相关产品】利培酮口服溶液、氨己烯酸口服溶液用散、阿托伐他汀钙片、利伐沙班片【自身资源】过评产品：医保、国谈，慢病系列【需要资源】全国临床、二三终端相关领域省级经销商、终端代理商超级会员9【会员编号】w0127【所在地区】山东【所在公司】山东誉众医药【工作职务】总经理【相关产品】骨科/肿瘤/抗生素/心血管/重症/透析/呼吸产品【自身资源】专业化的省级医药推广服务商。自营1条线+招商3条线+市场部1条线+集采产品专项。学术推广能力、政务关系、商业资源优秀。【需要资源】优质的相关产品升级代理。超级会员10【会员编号】w0009【所在地区】浙江【所在公司】浙江明晖医药有限公司【工作职务】总经理【相关产品】全国总代:阿昔洛韦颗粒、别嘌醇片；自有持证：他达拉非片【自身资源】1.浙江省临床品种推广网络；2、全国总代理产品；3、自有批文；4、零售电商公司；5、C端电商供应链【需要资源】1、需要在浙江代理推广的甲方产品；2、全国省级代理合作伙伴超级会员11【会员编号】w0172【所在地区】江苏南京【所在公司】西安良医网络科技集团有限公司【工作职务】营销中心负责人【相关产品】1.米墨 2.超医助手【自身资源】有一个医药互联网服务交易溯源平台“米墨”为行业发展提供新方案、新模式，为药械厂商提供深度学术推广及精准营销升级服务；以及医生资源平台“超医助手”目前大约有数百万的医疗行业从业者资源。拥有各类医疗互联网平台资源，企业资源，医药企业资源。【需要资源】链接医药企业超级会员12【会员编号】w0173【所在地区】上海市静安区【所在公司】上海鑫意医药科技有限公司【工作职务】董事长【相关产品】关节镇痛巴布膏、强力天麻杜仲胶囊等【自身资源】招标、医疗终端等【需要资源】需要上家优质产品，需要有管理能力的业务经理超级会员13【会员编号】w0029【所在地区】湖南【所在公司】湖南思达医药有限公司【工作职务】销售总监【相关产品】主营产品线：儿科，骨科，妇科，内科等【自身资源】湖南思达医药公司主营临床新药推广，团队覆盖湖南省14个地区，团队结构：地区经理10人，专业学术经理2人，商务经理2人；现有代理推广品种包含国采，省际联盟集采，基药，医保等类型，主营产品线：儿科，骨科，妇科，内科等；具备湖南药品招标准入能力。【需要资源】上游厂家，国代，批文持有人，原料商等，品种需要在湖南落地推广的。超级会员14【会员编号】w0174【所在地区】山西太原【所在公司】山西龙行医药【工作职务】总经理【相关产品】省代临床，OTC。呼吸科，心血管等【自身资源】地政，临床开发，OTC操作【需要资源】代理优秀品种，山西市场跨渠道运营超级会员15【会员编号】w0202【所在地区】广西【所在公司】广西花红药业集团有限公司【工作职务】业务部总经理【相关产品】花红胶囊，花红颗粒，消肿止痛酊，解毒生肌膏，葛根芩连丸【自身资源】独家医保，基药，企业品牌优势，全国有成熟的商务体系及招商资源【需要资源】寻求有资源的妇科，骨科，肛肠，慢创，儿科等合作优质客户超级会员16【会员编号】w0166【所在地区】杭州【所在公司】浙江和融达医疗技术有限公司【工作职务】董事长【相关产品】消化领域、心脑血管、骨科的药品和器械耗材【自身资源】成立了MAH上市持有人与院内制剂转化平台，成熟的全国销售网络，目前每年立项研发的药品和器械2-3个【需要资源】1、全国各省医疗器械和药品销售精英及MAH合伙人。2、一流研发机构和优秀生产企业战略合作。超级会员17【会员编号】w0048【所在地区】杭州【所在公司】浙江万晟药业有限公司【工作职务】总监【相关产品】蔓迪、芪明颗粒【自身资源】市场准入、政策法规【需要资源】市场准入（医保、招采）超级会员18【会员编号】w0216【所在地区】江苏南京【所在公司】武汉天安医药【工作职务】市场总监【相关产品】B证持有人公司，拥有泮托拉唑、奥美拉唑、倍他米松、阿托品等品种，奥美拉唑、阿托品为国采中选产品【自身资源】定位B证公司合作平台，可一起合作开发立项【需要资源】各省代理商资源，其中湖北、江苏拥有精细化招商团队，也可代理品种超级会员19【会员编号】w0221【所在地区】浙江【所在公司】浙江敬紫堂生物科技有限公司【工作职务】总经理【相关产品】酒制蜂胶【自身资源】全国临床和三终端代理商资源【需要资源】更多的终端资源    超级会员20【会员编号】w0133【所在地区】河北【所在公司】河北东鼎医药科技有限公司【工作职务】销售总监【相关产品】喷他佐辛注射液、盐酸曲马多注射液、氯化钾颗粒、香丹注射液等【自身资源】河北省内完善的等级医院客户资源，包括镇痛类、心血管、抗生素等优质的销售网络。【需要资源】镇痛类产品，集采产品，高端学术产品。超级会员21【会员编号】w0231【所在地区】河南郑州【所在公司】河南诚济医药有限公司【工作职务】销售总监【相关产品】临床基药产品销售推广业务【自身资源】具有完善的河南省临床基药销售渠道【需要资源】在河南有新特药、基药产品需要推广销售的上游企业可接洽超级会员22【会员编号】w0110【所在地区】河南【所在公司】医药园区【工作职务】顾问【相关产品】三方业务；共享仓设立GSP公司【自身资源】政策红利（共享仓、按月返税）【需要资源】客户资源超级会员23【会员编号】w0179【所在地区】福州【所在公司】福建润辉商务管理有限公司【工作职务】总经理【相关产品】环丙沙星缓释片（悉复欢）500mg*6片/12片【自身资源】全国总代产品资源【需要资源】各省份/各区域代理商超级会员24【会员编号】W0235【所在地区】河北【所在公司】海南凯瑞医药【工作职务】营销总监【相关产品】首儿药业全系儿科产品【自身资源】河北、山东药械资源【需要资源】各省医药口服产品代理商，医院、诊所、零售、院外等渠道合作伙伴扫码加高端会员获取更多医药资源信息