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Alector (ALEC)

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Earnings summaries and quarterly performance for Alector.

Recent press releases and 8-K filings for ALEC.

Alector's Phase 3 INFRONT-3 Trial Misses Co-Primary Endpoint, Leading to Investigation
ALEC
Legal Proceedings
Demand Weakening
  • Alector, Inc. (ALEC) is under investigation by Levi & Korsinsky, LLP following the announcement of topline results from its Phase 3 INFRONT-3 trial.
  • The Phase 3 INFRONT-3 trial for latozinemab, evaluating its efficacy in slowing progression of frontotemporal dementia (FTD-GRN), failed to achieve its clinical co-primary endpoint.
  • While the biomarker response co-primary endpoint was met, the clinical response endpoint was not met, leading analysts to express disappointment and downgrade ALEC's stock after the results were reported on October 21, 2025.
Jan 29, 2026, 11:06 PM
Alector Therapeutics discusses pipeline and financial runway at BofA 2025 CNS conference
ALEC
New Projects/Investments
Guidance Update
  • Alector Therapeutics is focused on developing therapeutics for neurodegenerative disorders, leveraging its proprietary Blood-Brain Barrier (BBB) technology to enhance drug delivery to the brain.
  • The company's pipeline includes a progranulin-elevating drug (AL101) in Phase 2 for Alzheimer's disease, with an interim analysis expected in the first half of 2026.
  • Alector is also advancing an anti-amyloid beta antibody (AL137) targeting the clinic in 2026, and a GCase enzyme replacement therapy (AL50) for Parkinson's disease, with first-in-human studies targeted for 2027.
  • The company reported approximately $300 million in cash, providing a financial runway through 2027 to support its clinical programs and achieve multiple value-creating milestones.
Dec 8, 2025, 7:25 PM
Alector Therapeutics Provides Pipeline Update and Financial Outlook
ALEC
Product Launch
New Projects/Investments
Guidance Update
  • Alector Therapeutics, a neurodegeneration-focused company, expects an interim analysis of its Phase 2 study for AL101, a progranulin-elevating drug for Alzheimer's disease partnered with GSK, in the first half of 2026.
  • The company's ABC platform utilizes blood-brain barrier technology to deliver large molecules to the brain at 10- to 50-fold higher concentrations, aiming for enhanced efficacy, lower dosing, and improved safety for neurodegenerative disorders.
  • Alector plans to advance its anti-amyloid beta antibody (AL137) into the clinic in 2026 and its GCase enzyme replacement therapy (AL50) for Parkinson's disease into first-in-human studies in 2027, both leveraging the ABC platform.
  • With approximately $300 million in cash, Alector has a financial runway through 2027 and anticipates achieving multiple value-creating milestones, including patient data for AL137, within this period.
Dec 8, 2025, 7:25 PM
Alector Therapeutics Provides Pipeline and Financial Updates
ALEC
New Projects/Investments
Guidance Update
  • Alector Therapeutics, a neurodegeneration-focused company, anticipates an interim analysis for its Phase II AL101 study in Alzheimer's disease during H1 2026.
  • The company's Blood-Brain Barrier (ABC) platform is advancing new programs, including an anti-amyloid-β antibody (AL137) expected to enter the clinic in 2026 and a GCase enzyme replacement therapy (AL50) for Parkinson's disease targeting first-in-human studies in 2027.
  • Alector reports a cash runway through 2027 with approximately $300 million in cash, which is expected to support multiple value-creating milestones across its clinical and preclinical programs.
Dec 8, 2025, 7:25 PM
Alector Reports Q3 2025 Financial Results and Strategic Business Updates
ALEC
Earnings
Layoffs
Guidance Update
  • Alector reported a net loss of $34.7 million, or $0.34 per share, for the third quarter of 2025. As of September 30, 2025, the company had $291.1 million in cash, cash equivalents, and investments, which is anticipated to fund operations through 2027.
  • In October 2025, Alector implemented a reduction in force of approximately 47% to focus resources and extend its cash runway.
  • The company is advancing lead candidates AL137 and AL050 toward IND-enabling studies, targeting IND submissions in 2026 and 2027, respectively.
  • Topline results from the Phase 3 clinical trial for latozinemab in frontotemporal dementia due to a GRN gene mutation did not demonstrate clinical benefit, leading to the discontinuation of the trial. An independent interim analysis for the PROGRESS-AD Phase 2 clinical trial of nivisnebart is planned for the first half of 2026.
Nov 6, 2025, 9:12 PM
Alector Reports Third Quarter 2025 Financial Results and Business Updates
ALEC
Earnings
Layoffs
Guidance Update
  • Alector reported a net loss of $34.7 million, or $0.34 per share, for the third quarter ended September 30, 2025, with collaboration revenue of $3.3 million.
  • The company's cash, cash equivalents, and investments totaled $291.1 million as of September 30, 2025, providing a runway through 2027.
  • Alector is advancing lead candidates AL137 and AL050 toward IND-enabling studies, with IND filings targeted for 2026 and 2027, respectively, and an independent interim analysis for the PROGRESS-AD Phase 2 clinical trial of nivisnebart (AL101) is planned for 1H 2026.
  • In October 2025, the company implemented a workforce reduction of approximately 47% and discontinued the INFRONT-3 Phase 3 clinical trial for latozinemab due to a lack of clinical benefit.
Nov 6, 2025, 9:05 PM
Alector Announces Negative Phase 3 Clinical Trial Results for Latozinemab
ALEC
New Projects/Investments
  • Biotechnology company Alector announced that its drug, latozinemab, failed to meet safety and efficacy criteria in a Phase 3 clinical trial for cases of FTD caused by a GRN gene variant.
  • While the treatment resulted in a significant increase in plasma PGRN levels, it did not slow the progression of the disease as measured by clinical co-primary endpoints or affect biological markers of disease progression.
  • Based on these results, Alector has concluded the study, and the open-label extension portion of the trial and the continuation study will both be discontinued.
Oct 21, 2025, 10:45 PM
Alector's Latozinemab Phase 3 Trial Fails to Meet Primary Endpoint
ALEC
Layoffs
Profit Warning
  • Alector's Phase 3 INFRONT-3 trial for latozinemab, targeting frontotemporal dementia (FTD) caused by GRN gene mutations, failed to meet its primary clinical endpoint of slowing disease progression.
  • Despite the drug significantly increasing plasma progranulin levels, it did not translate into clinical benefit or affect other biomarkers.
  • In response to the trial failure, Alector announced it would terminate the open-label extension of the trial and lay off 49% of its 238 employees.
  • The 96-week double-blind study, conducted in collaboration with GSK, found the treatment to be safe with no major adverse events reported.
Oct 21, 2025, 9:53 PM
Alector Announces Latozinemab Phase 3 Trial Results and Business Update
ALEC
Layoffs
Management Change
Guidance Update
  • Alector announced that its latozinemab (AL001) Phase 3 INFRONT-3 clinical trial for frontotemporal dementia due to a GRN mutation did not meet its clinical co-primary endpoint, leading to the discontinuation of the open-label extension and continuation studies for latozinemab.
  • To align resources with strategic priorities, Alector is implementing a workforce reduction of approximately 49%, impacting about 75 employees.
  • Total incremental restructuring charges associated with the reduction in force are expected to be approximately $7.7 million, with cash payments anticipated in the first half of 2026.
  • The company estimates it had approximately $291.1 million in cash, cash equivalents, and short-term investments as of September 30, 2025, which is expected to provide a financial runway through 2027.
  • Sara Kenkare-Mitra, Ph.D., President and Head of Research and Development, will resign from her role effective December 22, 2025.
Oct 21, 2025, 8:08 PM
ALEC Holdings Debuts on DFM After $381M IPO
ALEC
Dividends
New Projects/Investments
  • ALEC Holdings debuted on the Dubai Financial Market (DFM) following the UAE's largest construction sector IPO, raising approximately $381 million through the sale of 20% of its share capital.
  • The IPO was heavily oversubscribed, with demand reaching around $8.1 billion, more than 21 times the offering size, and attracted high non-UAE investor participation.
  • The company, majority-owned by the Investment Corporation of Dubai (ICD) which retains an 80% stake, has a significant project backlog of AED 35.4 billion.
  • ALEC Holdings plans to distribute substantial dividends starting in 2026, with a minimum payout ratio of 50 percent of net profit, paid biannually in April and October.
  • On its debut day, shares opened at 1.47 dirhams and traded as high as 1.50 dirhams, closing slightly above the IPO price, reflecting strong investor interest.
Oct 15, 2025, 7:13 AM