Gilead Sciences (GILD) closed the latest trading day at $73.41, indicating a +0.2% change from the previous session's end. The stock's change was less than the S&P 500's daily gain of 0.57%. Meanwhile, the Dow gained 0.83%, and the Nasdaq, a tech-heavy index, added 0.39%. Heading into today, shares of the HIV and hepatitis C drugmaker had gained 2.35% over the past month, outpacing the Medical sector's gain of 0.13% and lagging the S&P 500's gain of 2.97% in that time. Market participants will be closely fo ...

LAFAYETTE, Colo.--(BUSINESS WIRE)--The Center for Disease Analysis Foundation (CDA Foundation) is thrilled to announce the first-round recipients of the CDAF-Relink grant to connect Hepatitis B and C infected individuals in the United States back to care. The program is funded by an eight-million-dollar grant from Gilead Sciences (Nasdaq: GILD) as part of Gilead’s Relink grant program. In this first round, CDA Foundation distributed a total of 2.1 million dollars to the following 14 grantees: Organization O ...

业绩总结 - Gilead预计到本年代末将实现加速增长[3] - Gilead拥有全球最大的HIV业务，未来将推出多款产品以推动额外增长[3] - Gilead拥有全球领先的细胞疗法业务，正在收购一家肝病公司，预计推出名为seladelpar的药物，以及在肝癌领域的产品Trodelvy[4] 未来展望 - Gilead的HIV领域未来增长重点在于一次性药物、预防性药物和广谱中和抗体[6] - Gilead计划在2023年底之前推出每6个月一次注射的预防性药物，预计将大幅扩大预防市场[17] - Gilead认为预防市场不仅适用于男同性恋和静脉注射药物使用者，还适用于所有有多个性伴侣或患有性传播疾病的人[21] 新产品和新技术研发 - Gilead计划在2023年底之前推出每6个月一次注射的预防性药物，预计将大幅扩大预防市场[17] - 针对Anito-Cel的数据表现令人鼓舞，具有较高的疗效和安全性[45] - Anito-Cel的构造与其他细胞疗法不同，具有更高的转导效率[46] 市场扩张和并购 - Gilead拥有全球领先的细胞疗法业务，正在收购一家肝病公司，预计推出名为seladelpar的药物，以及在肝癌领域的产品Trodelvy[4] - Gilead的细胞疗法业务在美国市场面临一些挑战，但预计在下半年将实现强劲增长，全球市场仍然表现强劲[35] - 公司计划在自身或外部合作伙伴的支持下，持续关注细胞疗法领域的发展[52]

产品信息 - Anito-Cel是一种BCMA构造，研究显示在iMMagine-1研究中，63%的患者属于高风险群体[7] - Anito-Cel的转导效率达到70%，远高于同类产品的15%[10] - D-Domain的独特性使其在温度或pH变化时保持稳定，具有简单且优越的结合结构[17] 市场扩张和并购 - Kite拥有全球生产设施和超过420个授权治疗中心，为推广Anito-Cel提供了机会[11] - 目前CAR-T在美国的市场份额停滞在15%至17%，Kite正致力于提高市场份额[19] - 公司正在在社区建立授权治疗中心，以便更好地服务社区[23] 未来展望 - 预计在今年下半年公布iMMagine-1数据，并已与监管机构商讨进入更早期的治疗线[12] - 预计Anito-Cel将具有等效或更好的疗效，并具有差异化的安全性[14] - 到2026年，预计每年能生产24000名CAR-T患者的产品[58] 其他新策略和有价值的信息 - 公司正在在社区建立授权治疗中心，以便更好地服务社区[23] - 公司计划投资于多发性骨髓瘤和自身免疫疾病领域[59] - 公司的目标是随着规模扩大，继续提高盈利能力[61]

Gilead Sciences, Inc.参加Leerink Partners Global Biopharma Conference - Anito-Cel的BCMA CAR-T疗法展示[5][6] Anito-Cel在iMMagine-1研究中表现出高效率和安全性 - 具有与竞争对手相媲美的疗效[7][8] Kite与Anito-Cel的合作 - 拥有全球生产设施和超过420个授权治疗中心，有望将Anito-Cel推广到全球更多患者[9] Kite计划在今年下半年分享iMMagine-1数据 - 已与监管机构讨论进入更早阶段的研究[10] Anito-Cel的D-Domain结构独特 - 具有高转导效率和低基础信号，使得剂量可以减半但依然保持高效的肿瘤细胞杀伤能力[8] Kite致力于提高CAR-T疗法的市场份额 - 通过在社区和学术中心推广CAR-T的使用，以及教育医生和患者，以增加CAR-T的接受率[15][16][17][18][19][20][21] Kite面临来自其他CAR-T产品和生物特异性产品的竞争 - 但认为提高CAR-T的使用率和教育意识是关键[22][23][24] Kite在社区推广CAR-T疗法的经验表明灵活性至关重要 - 但已经制定了一套可复制的操作方案，并与其他医院系统和社区实践进行合作[29][30] Kite认为CAR-T疗法与干细胞移植不同 - 社区实践不需要成为移植中心，因此CAR-T的推广路径将有所不同[31][32] Kite将重点放在大型社区实践的推广上 - 认为这些实践具有基础设施和患者资源，有望成为CAR-T的主要提供者[32][33] Kite认为随着BCMA社区的扩大 - 可能会对Yescarta和Tecartus产生短期负面影响，但他们正努力扩大CAR-T的使用范围，以弥补这种影响[35] Vanderbilt和HCA医院系统已经在提高门诊患者容量方面取得了成功 - [36] CAR-T治疗对于多发性骨髓瘤和自身免疫疾病的应用前景广阔 - [37] Kite正致力于扩大CAR-T治疗在社区医疗实践中的应用 - [39] Kite与Moffitt等医疗机构合作 - 探索在自身免疫疾病领域的合作机会[40] Kite正在与FDA讨论如何改进CAR-T治疗的安全性和监管 - [42] Kite计划在自身免疫疾病领域进行投资 - 以提高盈利能力[48] Kite的CAR-T治疗生产能力不断提升 - 预计到2026年每年可达到2.4万例[51] Kite将继续投资于多发性骨髓瘤和自身免疫疾病领域 - [52] Kite在研发领域探索新的CAR-T治疗构建 - 包括三天制造过程和双重/三重靶向[62] Kite在研发新的CAR-T治疗构建 - 如CD19与IL-18和IL-15的结合，以增强治疗效果[65] Kite正积极探索Allo疗法 - 以满足自身免疫疾病无法覆盖的需求[68] Allo今天的效力并不像自动构建那样有效 - [69] 对于高度侵袭性疾病的患者 - 仍然需要淋巴去除[70] 在骨髓瘤患者中 - 可能需要更好的过渡疗法[71]

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the required waiting period under the Hart-Scott-Rodino Antitrust Improvements Act of 1976 (HSR Act) with respect to Gilead’s cash tender offer for CymaBay Therapeutics, Inc. expired at 11:59 p.m. on March 8, 2024. On February 22, 2024, Gilead and CymaBay filed the Premerger Notification and Report Forms required under the HSR Act with the Federal Trade Commission and the Antitrust Division of the U.S. Department ...

In the latest trading session, Gilead Sciences (GILD) closed at $73.66, marking a +1.42% move from the previous day. The stock outpaced the S&P 500's daily gain of 1.03%. Meanwhile, the Dow gained 0.34%, and the Nasdaq, a tech-heavy index, added 1.51%. Prior to today's trading, shares of the HIV and hepatitis C drugmaker had lost 2.41% over the past month. This has lagged the Medical sector's gain of 2.1% and the S&P 500's gain of 3.21% in that time. Investors will be eagerly watching for the performance of ...

Gilead Sciences (GILD) and Merck (MRK) announced promising first data from a phase II study evaluating the combination of a once-weekly treatment regimen of Merck’s islatravir and Gilead’s lenacapavir. The data demonstrated the efficacy of this potential long-acting oral combination treatment option in maintaining viral suppression in individuals with HIV. At the 24-week mark, the combination of islatravir and lenacapavir showcased an impressive 94.2% rate of viral suppression (HIV-1 RNA <50 copies/mL), wit ...

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced new data from three studies evaluating the efficacy and safety profile of Biktarvy® (bictegravir 50 mg/emtricitabine 200 mg/tenofovir alafenamide 25 mg tablets, B/F/TAF) for a broad range of people with HIV, including those with HIV/hepatitis B (HBV) coinfection and HIV/tuberculosis (TB) coinfection. These data and other studies supporting the important role of Biktarvy in the HIV treatment landscape were presented at ...

FOSTER CITY, Calif., & RAHWAY, N.J.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) and Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced results from the Phase 2 clinical study evaluating the investigational combination of islatravir, an investigational nucleoside reverse transcriptase translocation inhibitor, and lenacapavir, a first-in-class capsid inhibitor. These late- breaking data were presented during an oral session at the 31st Conference on Retroviruse ...