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ALEC

Alector, Inc.

Biopharma developer (SEC filing verified)·Phase 3·South San Francisco, CA, United States·CEO: Dr. Arnon Rosenthal Ph.D.
Neurology

ALEC evidence brief

What we can confirm

BioSniper Score:
4.5 / 10
Market Cap:
$275.8M
Lead Asset:
al064 (Preclinical)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $275.8M · Lead Asset: al064 (Preclinical)
BioSniper AIPage evidence connected

Prepared research question

What matters most for ALEC—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · ALEC

Alector, Inc. is a publicly traded biotechnology company focused on developing therapies for neurodegenerative diseases, with a wholly owned blood-brain barrier platform and a pipeline of programs targeting Alzheimer's, Parkinson's, and related disorders.

Key risk: Cash runway

4.5/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$275.8M

Cash Runway

—

Lead Asset

al064 (Preclinical)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 9 clinical trials for Alector, Inc..

AI OverviewAI overview is shown in English only.

Alector, Inc. is a publicly traded biotechnology company focused on developing therapies for neurodegenerative diseases, with a wholly owned blood-brain barrier platform and a pipeline of programs targeting Alzheimer's, Parkinson's, and related disorders.

  • Cash & equivalents of $59.9M as of 2026-06-30 [sec]
  • Total revenue of $3.3M and net income of -$23.0M as of 2026-06-30 [sec]
  • Accumulated deficit of $1,018.0 million as of 2026-08-06 [sec_mda]
  • Lead anti-amyloid beta antibody AL137 advancing toward IND submission targeted for Q1 2027 [sec_mda · as of 2026-08-06]
  • Virtual R&D event scheduled for October 7, 2026 to highlight ABC-enabled pipeline including AL137, AL164, and AL062 [news · published 2026-10-07]

What works

  • Alector's wholly owned ABC blood-brain barrier platform enables peripheral dosing for siRNA and antibody programs, potentially offering more convenient and scalable administration compared with intrathecal delivery [sec_mda · as of 2026-08-06]
  • The company has multiple wholly owned programs advancing toward IND-enabling studies, including AL137 (anti-amyloid beta antibody) and AL050 (GCase enzyme replacement therapy) [news · published 2025-11-06]
  • Alector has a pipeline of siRNA programs targeting tau, alpha-synuclein, and NLRP3 for neurodegenerative disorders [news · published 2025-11-06]

What to weigh

  • Alector has an accumulated deficit of $1,018.0 million as of 2026-08-06, with net losses substantially from R&D and G&A costs [sec_mda · as of 2026-08-06]
  • Cash & equivalents have declined from $354.6 million in Q1 2025 to $59.9 million as of 2026-06-30, indicating significant cash burn [news · published 2025-05-08] [sec]
  • Shareholders' equity is negative at -$10.0M as of 2026-06-30, reflecting accumulated losses exceeding equity [sec]
  • The company expects expenses to increase substantially as it advances preclinical studies, clinical trials, and regulatory activities [sec_mda · as of 2026-08-06]

From the filings

Quoted directly from source documents.

  • Accumulated deficit

    “2026, we had an accumulated deficit of $1,018.0 million.”

    SEC MD&A · August 6, 2026

  • Lead anti-amyloid beta antibody AL137 IND target

    “we intend to advance AL137 for submission of an Investigational New Drug (IND) application, targeted for the first quarter of 2027.”

    SEC MD&A · August 6, 2026

  • Virtual R&D event

    “Alector to Host Virtual Research and Development Event Highlighting Wholly Owned Alector Brain Carrier (ABC)- Enabled Pipeline”

    News · October 7, 2026

  • Cash position decline

    “Extending runway into the second half of 2027, with $354.6 million in cash, cash equivalents, and investments”

    News · May 8, 2025

Catalyst timeline

  • 2019-09-27 · Phase 2 start for AL001 in FTD (heterozygous carriers of GRN or C9orf72 mutations) — This is a historical catalyst; no recent update on this trial's status is provided in the chunks.
  • 2021-01-22 · Phase 2 start for AL002 in early Alzheimer's disease — This is a historical catalyst; no recent update on this trial's status is provided in the chunks.
  • 2021-09-02 · Phase 2 start for AL001 in C9orf72-associated ALS — This is a historical catalyst; no recent update on this trial's status is provided in the chunks.
  • 2023-01-04 · Phase 2 start for a multicenter, long-term study — This is a historical catalyst; no recent update on this trial's status is provided in the chunks.
Risks & what to watch (4)›

Key risks

  • Cash runway — Cash & equivalents dropped from $354.6M (Q1 2025) to $59.9M (2026-06-30), raising concerns about near-term funding [news · 2025-05-08] [sec]
  • Negative equity — Shareholders' equity of -$10.0M as of 2026-06-30 indicates liabilities exceed assets [sec]
  • Rising expenses — Expenses expected to increase substantially as the company advances R&D and regulatory activities [sec_mda · 2026-08-06]
  • Clinical trial risk — Key Phase 2/3 trials (e.g., INFRONT-3, PROGRESS-AD) have not yet reported topline data; delays or negative outcomes could impair pipeline value [news · 2025-08-07]

What to watch

  • Topline data from the INFRONT-3 Phase 3 trial of latozinemab in FTD-GRN, previously on track for Q4 2025 [news · published 2025-08-07]
  • Completion of the PROGRESS-AD Phase 2 trial of AL101 in early Alzheimer's disease, expected in 2026 [news · published 2025-08-07]
  • IND submission for AL137 targeted for Q1 2027 and first-in-human dosing in Australia no later than April 2027 [sec_mda · as of 2026-08-06]
  • Virtual R&D event on October 7, 2026, which may provide updates on ABC-enabled pipeline programs [news · published 2026-10-07]

Sources: Catalysts · News · Pipeline · SEC MD&A · Generated October 11, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health2.0

Net income -$23M

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth5.9

3 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal1.5

0 buys · 5 sells (180d)

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

137

Total value held

$181.0M

Showing top 10 of 137 institutional holders of Alector, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 19, 2026
% of float
7.0%
Days to cover
8.2
Shares short
6,284,391
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

ALEC short interest

Governance

Frequently asked questions

What is the AI investment thesis for Alector, Inc.?

Alector, Inc. is a publicly traded biotechnology company focused on developing therapies for neurodegenerative diseases, with a wholly owned blood-brain barrier platform and a pipeline of programs targeting Alzheimer's, Parkinson's, and related disorders.

What is Alector, Inc.'s lead drug candidate?

Alector, Inc.'s most advanced tracked candidate is al064 (Preclinical) for Alzheimer's disease and other tauopathies.

Who is the CEO of Alector, Inc.?

Dr. Arnon Rosenthal Ph.D. is the chief executive officer of Alector, Inc. (ALEC).

Where is Alector, Inc. headquartered?

Alector, Inc. (ALEC) is headquartered in South San Francisco, CA, United States.

What therapeutic areas does Alector, Inc. focus on?

Alector, Inc. develops therapies across Neurology.

923 companies304,846 SEC filings22,682 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.