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北京时间·🕒 发布 05:20:31时区推断·⟳ 抓取 05:22:43·⚡ 决策 07-09 05:24:24 +1m41s·110.6 天前

GSK将终止与Alector的两款神经科学抗体药物合作

对Alector(ALEC.US)方向是明确利空:GSK终止2021年合作,意味着latozinemab和nivisnebart相关的最高15亿美元里程碑、美国利润分成和海外royalty期权基本消失。

📄 原文Reuters↗ 原文
Alector (ALEC.O) said on Wednesday that GSK (GSK.L) had terminated their neuroscience collaboration agreement covering…
观望 Alector(ALEC.US)
事件方向明确利空,但两项临床失败已提前披露,本次终止是后续确认;默认不开空且未确认可借券,不能给ENTER SHORT。
不做 葛兰素史克(GSK.GB)
终止失败合作对GSK属于小型研发管线止损,相对市值和收入基数太小,没有短周期可量化交易edge。
展开详情(成交明细 / 研究档案 / 原文全文 / 决策记录链)

研究档案

🔎 新鲜度:最早出现 2026-07-08 · 扩散 medium · price-in 风险 medium ↗ ↗

消息传播链

  1. 2026-07-08首发Reuters非一手原文 ↗
    Reuters报道Alector称GSK已发出终止通知,涉及latozinemab和nivisnebart两款抗体药物合作。
    市场反应:ALEC.US当日收于1.83美元,较前收跌5.18%。
  2. 2025-09-30其它SEC一手源原文 ↗
    Alector此前披露GSK协议包含7亿美元首付款、最高15亿美元里程碑、美国利润分成和海外双位数royalty,说明该合作曾是重要资产。

关键理由

  • 对Alector(ALEC.US)方向是明确利空:GSK终止2021年合作,意味着latozinemab和nivisnebart相关的最高15亿美元里程碑、美国利润分成和海外royalty期权基本消失。
  • 量级上,Alector此前未产生产品销售收入,GSK协议截至2025年三季度仍有约1.79亿美元递延收入,是公司近年收入叙事核心之一;但两项临床失败和裁员已先行披露,本次终止更多是失败后的合同兑现。
  • 对GSK(GSK.L)体量太小且偏止损研发管线,难以构成市值级短线催化。

主要风险

  • Alector股价已在事件前后处于低价高波动状态,7月8日已跌5.18%,且latozinemab失败、nivisnebart中期分析失败均是旧信息,终止通知的新鲜增量有限。
  • 默认不开空仓,行情工具未返回可借券字段,不能满足做空红线。

反向证据

  • 做空前查反向 · 来源 stock_quote · 日期 2026-07-08 · 影响 weakens
    行情工具未返回可借券数量或可融券确认,不能满足做空红线。
    检索:Alector GSK termination borrow short sell availability ALEC
工具调用 · 历史记录,结果未知(1 种)
  • stock_quote · 结果未知

原文全文

展开原文 · 1,217 字
Alector (ALEC.O) said on Wednesday that GSK (GSK.L) had terminated their neuroscience collaboration agreement covering ​two experimental antibody drugs after both ‌the drug candidates suffered clinical setbacks.

The decision follows the failure of a late-stage study of latozinemab ​in a rare inherited form of ​frontotemporal dementia last year and the discontinuation of ⁠a mid-stage Alzheimer's disease trial of ​nivisnebart in April.

Here are further details:

GSK's termination notice ​relates to the companies' 2021 collaboration and license agreement for the development of monoclonal antibodies latozinemab and ​nivisnebart.

As per the terms of the deal ​announced in 2021, Alector received $700 million upfront from GSK ‌and ⁠could have received up to $1.5 billion in further payments tied to drug development-related milestones and royalties.

The failure of latozinemab prompted Alector ​to cut nearly ​half ⁠its workforce, while the nivisnebart trial was discontinued after an interim ​analysis showed the study was unlikely ​to ⁠meet its primary goal.

The termination will take effect on January 2 next year, following ⁠a 180-day ​notice period that began ​when GSK provided written notice on July 6.

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