Kura Oncology (NasdaqGS:KURA) Q3 2025 Earnings Call November 04, 2025 08:00 AM ET Speaker5Good day, everybody. My name is Danny, and I will be your conference operator today. At this time, I would like to welcome you to the Kura Oncology Third Quarter 2025 conference call. All lines have been placed on mute to prevent any background noises. After the speakers' remarks, there will be a question-and-answer session. If you would like to ask a question during this time and have joined via the webinar, please us ...

AI-driven precision-oncology analysis identifies patient subtypes with potential enhanced response to glufosfamide Accepted ASCO abstract, submitted in collaboration with Eleison Pharmaceuticals, provides further validation of BullFrog AI’s technology GAITHERSBURG, Md., Nov. 04, 2025 (GLOBE NEWSWIRE) -- BullFrog AI Holdings, Inc. (NASDAQ: BFRG; BFRGW) ("BullFrog AI" or the "Company"), a technology-enabled drug development company using artificial intelligence (“AI”) and machine learning to enable the succes ...

Prelude to prioritize development of mutant selective JAK2V617F JH2 inhibitor and KAT6A selective degrader programs Pausing further clinical development of SMARCA2 selective degrader programs JAK2V617F option agreement with Incyte, as previously announced, includes upfront payment of $35 million, a $25 million equity investment and $100 million if option is exercised Cumulative capital expected to fund planned operations into 2027 based on the Company’s preliminary estimates, and potentially into the third ...

Incyte secures an exclusive option to acquire Prelude’s mutant selective JAK2V617F JH2 inhibitor program Mutant selective JAK2V617F JH2 inhibitors have disease-modifying potential in treating patients living with myeloproliferative neoplasms (MPNs) Prelude to receive a $35 million upfront payment and $25 million strategic equity investment, $100 million if Incyte were to exercise the option to acquire the program, and up to $775 million in additional potential milestones plus royalties on net salesPrelude w ...

Following this approach, Acrivon has advanced two drug candidates into human clinical trials. Its lead program, ACR-368, is a selective CHK1/CHK2 inhibitor being evaluated in a registrational-intent Phase 2b trial for patients with recurrent, high-grade endometrial cancer who have progressed after platinum chemotherapy and immunotherapy. Early clinical readouts from the trial have been encouraging. Among patients identified as OncoSignature-positive, ACR-368 has delivered substantially higher response rates ...

Key Points Guardant's oncology and screening businesses are expanding at a rapid pace. New partnerships should drive further gains. 10 stocks we like better than Guardant Health › Shares of Guardant Health (NASDAQ: GH) rocketed 28% higher on Thursday after the precision oncology company reported outstanding growth metrics across its key product lines. Image source: Getty Images. Doing well by doing good Guardant's third-quarter revenue soared by 39% year over year to $265.2 million. The gains we ...

研究发布与临床验证 - 公司宣布其关于BE-Smart检测的研究已在线发表于美国胃肠病学会的官方期刊《临床与转化胃肠病学》[1] - 该研究提供了BE-Smart检测的完整临床验证数据，该检测是一种基于质谱的8蛋白组学检测，用于巴雷特食管患者的风险分层[2] - 研究是与梅奥诊所合作进行的，表明BE-Smart提供了一种高精度的分子驱动方法，可识别最有可能进展为高度不典型增生或食管腺癌的巴雷特食管患者[2] 检测技术优势与性能 - 与传统检测相比，BE-Smart仅需极少量组织（仅需现有检测所需材料的十分之一）即可实现全面的分子分析[3] - 该检测与钳子和刷子活检标本均兼容，不改变临床工作流程，并可使用标准福尔马林固定样本[3] - BE-Smart评估的是细胞增殖和免疫信号的新型蛋白质特征，而非长期建立的非特异性组织学标记物[3] - 检测显示出100%的灵敏度，成功识别出所有最终进展为食管癌的患者，未观察到假阴性[5] - 检测在多个分析中表现出强大的预测性能，总体曲线下面积为0.75，在独立测试队列中AUC达到0.89，对于三年内进展的患者AUC达到1.0[5] - 被BE-Smart归类为高风险的患者进展为食管癌的可能性是低风险患者的约66倍（风险比为66.1）[5] 商业化计划与市场影响 - 公司正在推进BE-Smart的广泛商业化和临床整合，重点关注实验室合作、支付方参与以及与领先胃肠病学网络的扩展真实世界研究[6] - 公司预计在2026年初开始早期访问计划和医生入职计划[6] - 每年有超过2万名美国人被诊断出食管癌，该疾病通常在晚期才被发现[7] - BE-Smart是公司STLA精准肿瘤学产品线中的首个发布成果[8]

Relay Therapeutics, Inc. (NASDAQ: RLAY ) is working at the cutting edge of precision oncology. RLY-2608, its lead asset, is an allosteric and pan-mutant PI3Kα inhibitor targeting breast cancer. This molecule is currently in phase 3 trials after producingDubai-based investor focused on building a resilient, income-generating portfolio with a long-term growth mindset. My approach is primarily long-only, blending dividend-paying equities, REITs, and other income strategies with selective growth opportunities. ...

Relay Therapeutics (NASDAQ: RLAY ) is working at the cutting edge of precision oncology. RLY-2608, its lead asset, is an allosteric and pan-mutant PI3Kα inhibitor targeting breast cancer. This molecule is currently in phase 3 trials, after producing positive interimDubai-based investor focused on building a resilient, income-generating portfolio with a long-term growth mindset. My approach is primarily long-only, blending dividend-paying equities, REITs, and other income strategies with selective growth opp ...

临床研究发表与商业化里程碑 - BE-Smart食管癌检测的关键临床研究被美国胃肠病协会官方期刊《Clinical Gastroenterology and Hepatology》接受发表[1] - 此里程碑标志着公司从技术验证阶段转向商业化阶段的关键转折点[2] - 公司计划在2026年开始分阶段推出该检测[2] 市场规模与商业化策略 - 美国每年约有700万例针对GERD和Barrett食管监测的上消化道内镜检查 为BE-Smart检测提供了约70亿至140亿美元的总可寻址市场[2] - 公司正在推进监管准备工作 并扩大实验室能力以支持临床检测 同时与领先的胃肠病诊疗机构合作[2] - 公司正寻求与关键意见领袖和医疗系统合作伙伴建立合作 以将BE-Smart整合到患者护理工作流程中[2] BE-Smart检测技术概述 - BE-Smart是一种基于质谱技术的8蛋白组学检测方法 通过与梅奥诊所的合作研究开发而成[3] - 该检测用于对Barrett食管患者进展为高度不典型增生或食管腺癌的风险进行分层[3] - 该检测是公司STLA精准肿瘤学产品管线中首个发表成果的项目[10] 临床研究关键数据 - 在100名患者的盲法队列中 BE-Smart检测在识别后续进展为癌症的患者方面达到100%的灵敏度[4] - 在独立测试中 该模型显示出强大的判别性能 测试队列中的AUC为0.89至1.0 其表现超过了预设的性能阈值[4] - 该检测在预测短期（三年内）疾病进展方面表现出高预测准确性 并且定量蛋白组学评分与进展时间之间存在强关联[4][8] 产品优势与临床价值 - BE-Smart检测与福尔马林固定石蜡包埋活检组织兼容 并可无缝集成到标准病理工作流程中[8] - 其高通量和多重设计适合临床实验室采用并具备可扩展性[8] - 该检测在组织学最不可靠的非发育不良和“发育不良不确定”病例中表现最佳[8] - 该检测无需额外组织 对医生和患者均友好[5] 行业需求与公司定位 - 当前Barrett食管的监测策略依赖于主观的组织学分级和频繁的内镜检查 这些方法具有侵入性、昂贵且通常不必要[7] - 胃肠病市场需要增强的分子分析来指导食管癌前病变的监测[5] - 公司是一家下一代生物技术、基因组学和消费产品公司 致力于通过全基因组测序解决方案和突破性诊断开发来革新医疗保健[11]