Lighthouse Pharma leverages translational insights and extensive clinical experience to better understand and treat dementia and other disorders. The team has a decade of data informing their strategy, including patient responder analyses, rigorous dose modeling, and clinical execution.

Company update from CEO Casey Lynch 2.6.2024

Leadership Team


UPDATE

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11/16/23

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UPDATE 〰️ 11/16/23 〰️

Lighthouse announces FDA approval to proceed with Phase 2 SPRING Trial of LHP588

The “Study May Proceed” notification from the FDA was based on review of the comprehensive IND package including safety, chronic toxicology, manufacturing, Phase 1 human data, and the planned Phase 2 SPRING (Stopping PRogression of P. gINGivalis-positive Alzheimer’s disease) trial protocol.

LHP588 is a next-generation gingipain inhibitor that has been optimized for selectivity and metabolism, demonstrating an excellent safety profile in both human and toxicology studies. With FDA clearance in hand, we look forward to working with our clinical advisors and investors to move this important clinical study forward.
— Casey Lynch, CEO of Lighthouse Pharmaceuticals

The planned Phase 2 SPRING clinical trial is a randomized, double-blind, placebo-controlled study to assess the efficacy and safety of once-a-day dosing of LHP588 for the treatment of P. gingivalis-positive mild to moderate Alzheimer’s disease. 300 patients will be enrolled in the trial and randomized into three arms (placebo, 25 and 50 mg) for 48 weeks of treatment. Patients must have mild to moderate Alzheimer’s disease and evidence of P. gingivalis infection, based on a saliva test. 


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