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Our vision

A world where people maintain healthy, resilient brains throughout their lifetime because neurodegenerative disease can be prevented and cured.

Kestrel Neuroscience funds focused, collaborative research into the causes of frontotemporal dementia (FTD) and related neurodegenerative diseases.

Our mission

To discover the causes of FTD and related neurodegenerative diseases and accelerate treatments, prevention, and cures through collaborative science.

Find the causes

Identify the genetic and molecular causes of FTD and closely related disorders such as amyotrophic lateral sclerosis (ALS).

Explain the biology

Work out the cellular mechanisms that drive neurodegeneration, so treatments can target the disease process itself.

Choose the targets

Discover, validate and prioritize new therapeutic targets, and move the strongest toward preclinical development.

Understanding FTD

The most common dementia in people under 60

Frontotemporal dementia damages the front and side regions of the brain. It changes personality, behavior, language and movement, often years before memory is affected, and it usually strikes in the middle of working and family life.

45–64

Typical age at onset. Many people are diagnosed while raising children and building careers.

~60,000

People living with FTD in the U.S. Diagnosis often takes years, so the true number is likely higher.

0

Approved treatments that slow or stop the disease. Today's care manages symptoms only.

Figures as published by the Association for Frontotemporal Degeneration (AFTD).

Learn about FTD from AFTD

Where we focus

We fund the gap between discovery and investment

In dementia and other neurodegenerative diseases, promising ideas often stall after they leave the academic lab. Explaining a disease mechanism is one thing. Turning it into a validated target and an early therapeutic candidate takes funding that research grants rarely cover and venture investors aren't yet ready to provide. Kestrel works in that gap, so the strongest discoveries reach the point where companies and investors can carry them forward.

The translational funding gap

  1. Stage 1

    Causes

    Genes and molecules behind FTD

  2. Stage 2

    Mechanisms

    How cells break down

  3. Stage 3

    Targets

    Validated points to intervene

  4. Stage 4

    Preclinical

    Early therapeutic candidates

  5. Stage 5

    Clinical trials

    Testing in people

  6. Stage 6

    Patients

    Approved treatments

Kestrel's focus Carried forward by companies, investors and clinical partners

Collaborative science

Leading laboratories, working on one problem together

Kestrel Investigators share data, methods and early results across institutions, guided by independent Scientific and Venture Advisory Boards.

  • Harvard Medical SchoolBoston
  • Max Planck Institute of BiophysicsFrankfurt
  • Memorial Sloan Kettering & Weill CornellNew York
  • Washington University in St. LouisSt. Louis
  • UT Southwestern Medical CenterDallas
5
Investigator laboratories
2
Countries
10
Scientific and venture advisors

Our model is deliberately small and connected. Rather than scattering single grants, Kestrel builds a standing group of investigators whose work fits together, so a finding in one lab can be tested in another within months.

Meet our investigators

Donate

Your gift goes to the science

Kestrel is a 501(c)(3) public charity. Contributions fund research into the causes of FTD and related neurodegenerative diseases, and are tax deductible to the extent allowed by law.

To give by check, make it payable to Kestrel Neuroscience Inc. and mail it to PO Box 2545, Carrollton, GA 30112.

Give $100 now Online giving opens soon. To give today, mail a check to the address below.

Keep up with the latest

News on Kestrel research, investigators and events, a few times a year.