reMYND

reMYND

Leuven, Belgium· Est.
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Private Company

Total funding raised: $60M

Overview

reMYND is a private, clinical-stage biotech developing novel oral therapeutics targeting synaptic and neuronal dysfunction in Alzheimer's and Huntington's disease. Its lead asset, REM392, is an oral small molecule designed to restore calcium homeostasis to provide both symptomatic and disease-modifying benefits in Alzheimer's. The company leverages a dual-strategy business model, combining internal drug development with a revenue-generating CRO service that validates its scientific platform and funds R&D.

Alzheimer's DiseaseHuntington's DiseaseAmyotrophic Lateral Sclerosis (ALS)

Technology Platform

Platform focused on developing oral small molecules that restore neuronal calcium (Ca²⁺) homeostasis to rescue synaptic dysfunction and reduce pathology in neurodegenerative diseases. Validated through proprietary in-vivo mouse models used in its CRO services.

Funding History

3
Total raised:$60M
Series C$30M
Series B$20M
Series A$10M

Opportunities

The Alzheimer's market is projected to grow to $15B by 2030, with a major unmet need for effective oral disease-modifying therapies.
reMYND's unique mechanism targeting calcium homeostasis and its dual business model (CRO + therapeutics) provide multiple paths to value creation and de-risking.

Risk Factors

High clinical development risk in neurodegenerative diseases, intense competition from larger players with more resources, and dependence on raising additional capital to advance its proprietary pipeline through costly clinical trials.

Competitive Landscape

In Alzheimer's, reMYND competes with large pharma (Biogen/Eisai, Lilly) with approved amyloid antibodies and a crowded pipeline of other modalities. Its oral, small molecule approach targeting synaptic function is a key differentiator. In Huntington's and ALS, it faces both large and small biotechs exploring genetic and non-genetic mechanisms.