Fundraising Everywhere's Community Fundraising Conference 17 June 2026

Longitude Prize on ALS awards £2 million to 20 teams pursuing ALS treatments

The Longiture Prize on ALS - announcing the 20 Discovery Award teams
Image: Challenge Works/The Longitude Prize on ALS

The Longitude Prize on ALS is designed to incentivise and reward cutting-edge, AI-based approaches to transform drug discovery for ALS, the progressive neurodegenerative disease that is currently without a cure.

A total of £2 million has been awarded to 20 highly promising multidisciplinary teams from 12 countries, including over 70 organisations such as King’s College London, Harvard Medical School, and Google Cloud. Each successful team receives £100,000 in funding and essential access to the largest and most comprehensive ALS patient dataset of its kind. This unprecedented dataset combines genomic sequences for 9,000 ALS patients with multi-omics data for over 2,000 cases, information that has never been available in a single place before.

The immediate goal for these teams is to leverage their expertise and AI to identify and validate new drug targets, thereby deepening the understanding of the disease and accelerating future drug discovery efforts. The complexity of ALS means that while limited treatments exist to slow progression temporarily, a long-term cure remains elusive. Advances in AI now offer an opportunity to unlock vast quantities of patient data and “outpace the disease”.

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Fundraising Everywhere's Community Fundraising Conference 17 June 2026

There is a 1 in 300 chance that a person will develop MND in their lifetime and around 90% of cases will have ALS.

Further funding rounds

The Longitude Prize on ALS is principally funded by the Motor Neurone Disease Association (MND Association) and is designed and delivered by Challenge Works, with support from Nesta

Additional funders include Nesta, The Alan Davidson Foundation, My Name’5 Doddie Foundation, LifeArc, FightMND, The 10,000 Brains Project, Answer ALS and The Packard Center at Johns Hopkins.

Further funding rounds are scheduled: ten teams will advance in 2027 to receive £200,000 each, and five teams will receive £500,000 in 2028 for target validation. The ultimate winner, who identifies and validates the target with the strongest therapeutic potential, will be announced in early 2031 and receive £1 million.

Tanya Curry, Chief Executive of the MND Association, restated the importance of the investment:

“Our vision is a world free from MND and this can be achieved through funding leading researchers to chase down new treatments. . . every step forward in research brings hope”.

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