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Inventiva, MoonLake Immunotherapeutics And Other Big Stocks Moving Lower In Monday's Pre-Market Session - Inventiva (NASDAQ:IVA), Cellectis (NASDAQ:CLLS)
Benzinga· 2025-09-29 12:06
U.S. stock futures were higher this morning, with the Dow futures gaining more than 100 points on Monday.Shares of Inventiva ADR (NASDAQ: IVA) fell sharply in today's pre-market trading following H1 results.Inventiva reported losses of $(1.84) per share compared to the analyst consensus estimate of loss of 41 cents per share. The company reported quarterly sales of $5.050 million which missed the analyst consensus estimate of $5.310 million.Inventiva shares dipped 5.5% to $5.72 in pre-market trading.Here ar ...
Inventiva, MoonLake Immunotherapeutics And Other Big Stocks Moving Lower In Monday's Pre-Market Session
Benzinga· 2025-09-29 12:06
U.S. stock futures were higher this morning, with the Dow futures gaining more than 100 points on Monday.Shares of Inventiva ADR (NASDAQ: IVA) fell sharply in today's pre-market trading following H1 results.Inventiva reported losses of $(1.84) per share compared to the analyst consensus estimate of loss of 41 cents per share. The company reported quarterly sales of $5.050 million which missed the analyst consensus estimate of $5.310 million.Inventiva shares dipped 5.5% to $5.72 in pre-market trading.Here ar ...
Lexicon reports FDA's decision to extend review period for Zynquista
Seeking Alpha· 2025-09-22 20:30
Lexicon Pharmaceuticals (NASDAQ:LXRX) said that the FDA has asked for additional time to review additional data for the potential resubmission of the marketing application for Zynquista (sotagliflozin) in adults with type 1 diabetes. This submission of additional clinical data follows ...
Lexicon Pharmaceuticals Announces Update on Submission of Additional Data to U.S. FDA Supporting the Benefit-Risk Profile of Zynquista® in Type 1 Diabetes
Globenewswire· 2025-09-22 20:00
Data obtained from ongoing third-party funded, investigator-sponsored trials have been submitted in effort to address the December 2024 complete response letter Company seeks alignment on reasonable path forward for Zynquista NDA resubmission FDA feedback from Type D meeting now expected during the fourth quarter THE WOODLANDS, Texas, Sept. 22, 2025 (GLOBE NEWSWIRE) -- Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX) today announced an update to the previous submission of additional clinical data to the U.S. Fo ...
Pilavapadin Provides Meaningful Pain Reduction in Adults with Diabetic Peripheral Neuropathic Pain (DPNP) in Data Presented at the European Association for the Study of Diabetes (EASD) and NEUROdiab Annual Meetings
Globenewswire· 2025-09-17 11:00
Pilavapadin 10 mg resulted in a two-point reduction from baseline in average daily pain scores (ADPS) by week 11 and was well tolerated in PROGRESS Phase 2b studyTHE WOODLANDS, Texas, Sept. 17, 2025 (GLOBE NEWSWIRE) -- Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX) today announced the presentation of clinical data from the company’s Phase 2b PROGRESS study for its investigational, AAK1-inhibitor, pilavapadin, for the treatment of diabetic peripheral neuropathic pain (DPNP) at two medical meetings: “New Promis ...
Lexicon Pharmaceuticals to Present Additional Clinical Data on Pilavapadin at Three Upcoming Medical Meetings
Globenewswire· 2025-09-11 12:30
Presentations collectively highlight pilavapadin’s potential to improve pain management care for patients with diabetic peripheral neuropathic pain (DPNP) Breadth of the data across Phase 2 program to be discussed at Arrowhead’s 19th Annual Pain Summit THE WOODLANDS, Texas, Sept. 11, 2025 (GLOBE NEWSWIRE) -- Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX) today announced the presentation of clinical data for its investigational, AAK1-inhibitor, pilavapadin, for the treatment of diabetic peripheral neuropathic ...
Lexicon Pharmaceuticals (NasdaqGS:LXRX) FY Conference Transcript
2025-09-08 19:32
Lexicon Pharmaceuticals (NasdaqGS:LXRX) FY Conference September 08, 2025 02:30 PM ET Company ParticipantsLander Egaña-Gorroño - Senior Associate - Biotech Equity ResearchMike Exton - CEO & DirectorConference Call ParticipantsNone - AnalystLander Egaña-GorroñoEveryone, my name is Lander. I'm a Senior Research Associate at H.C. Wainwright. We're pleased to have you with us today, and it is now my pleasure to introduce our next presenter. Please join me in welcoming Mike Exton, CEO of Lexicon Pharmaceuticals, ...
Lexicon Pharmaceuticals Announces Submission of Additional Data to U.S. FDA Supporting the Benefit-Risk Profile of Zynquista® in Type 1 Diabetes
Globenewswire· 2025-09-08 12:30
Data obtained from ongoing third-party funded, investigator-sponsored trials have been submitted in effort to address the December 2024 complete response letter Company seeks alignment on reasonable path forward for Zynquista NDA resubmission FDA feedback from Type D meeting expected by end of September THE WOODLANDS, Texas, Sept. 08, 2025 (GLOBE NEWSWIRE) -- Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX) today announced that the Company has submitted additional clinical data to the U.S. Food and Drug Adminis ...
Lexicon Pharmaceuticals to Present New Preclinical Data on Pilavapadin in Chemotherapy-Induced Pain and Multiple Sclerosis Pain at NeuPSIG 2025
Globenewswire· 2025-09-04 12:30
核心观点 - Lexicon Pharmaceuticals宣布其在研药物pilavapadin在化疗诱导周围神经病变和多发性硬化临床前模型中显示减轻神经性疼痛效果 该药物通过抑制新型靶点AAK1调节疼痛信号 公司同时将公布其针对糖尿病周围神经病变疼痛的2b期研究设计[1][2][3] 药物研发进展 - Pilavapadin在化疗诱导周围神经病变和多发性硬化临床前模型中表现出减轻神经性疼痛的效果[1] - 药物获得美国FDA快速通道资格 用于开发治疗糖尿病周围神经病变疼痛[4] - 公司将于2025年9月6日在柏林神经性疼痛国际会议上展示相关研究海报[7] 药物特性 - Pilavapadin是一种强效每日一次口服选择性小分子AAK1抑制剂 通过抑制神经递质再摄取和回收来调节疼痛信号 不影响阿片通路[3] - 临床前研究显示药物具有中枢神经系统渗透性 在神经性疼痛模型中减轻疼痛行为[3] - AAK1抑制剂被证明是治疗多种神经性疼痛疾病的有效靶点[2] 公司研发能力 - Lexicon拥有独特的基因组学靶点发现平台Genome5000™ 研究了近5000个基因的作用和功能 识别出100多个具有重要治疗潜力的蛋白质靶点[5] - 公司研发管线包含多个在神经性疼痛 肥厚型心肌病 肥胖 代谢等领域的临床前和临床阶段候选药物[5] - 公司专注于通过精确靶向蛋白质来发现和开发创新药物[5]
Lexicon Pharmaceuticals, Inc. (LXRX) Presents At Citi's Biopharma Back To School Conference Transcript
Seeking Alpha· 2025-09-03 23:36
公司战略调整 - 公司年初重新定位为纯研发型企业 专注于管线开发 [1] - 战略调整后三大主要资产管线取得重大进展 [1] 研发管线进展 - LX9851为临床前阶段资产 针对肥胖及相关适应症 [1] - 第一季度与诺和诺德签署全球独家授权协议 [1] - 授权覆盖LX9851资产的全球范围 [1] 运营时间节点 - 前三分之二年度业务繁忙 [1] - 后三分之一年度预计将保持高度忙碌状态 [1] - 资产开发按时间顺序推进 LX9851为年初首个重要节点 [1]