MCM6 is an early-stage biotechnology company developing differentiated small-molecule and antisense oligonucleotide (ASO) therapeutics. Backed by an STTR grant from the National Institute on Aging (NIA/NIH), we are advancing disease-modifying candidates in a multi-billion-dollar market with profound unmet need.
MCM6 is pioneering targeted therapeutics to address the core mechanistic driver of Alzheimer’s in APOE4 carriers—the largest genetic risk group.

In 1906, Dr. Alois Alzheimer identified the neuropathological hallmarks of the disease that now bears his name—a devastating condition marked by lipid dysregulation and one of humanity’s most profound medical and societal challenges. MCMVI, the Roman numeral for that pivotal year, embodies the founding spirit of MCM6. We confront these challenges through innovative science and restore hope for patients and families worldwide.
MCM6 is an early-stage biotechnology company driven by a bold vision: to redefine Alzheimer’s disease and related cognitive impairments by restoring lipid homeostasis. We are dedicated to delivering transformative, precision therapeutics that address the root causes of neurodegeneration.
Lipid homeostasis in the human brain—the tightly regulated balance of lipid synthesis, uptake, transport, metabolism, and clearance—is essential for membrane integrity, myelination, synaptic function, and metabolic health. Lipids comprise nearly half of the brain’s dry weight.
APOE4 represents a genetically stratified population suited for precision-medicine interventions. In APOE4 carriers, impaired lipid transport and clearance result in lipid droplet accumulation, glial dysfunction, chronic neuroinflammation, impaired amyloid clearance, and progressive neuronal loss. Current approved therapies do not address this fundamental driver, creating a significant unmet medical need.
MCM6 is developing differentiated small-molecule and ASO therapeutics designed to restore lipid balance specifically in APOE4 carriers. By enhancing APOE function, improving lipid transport, and modulating downstream pathways, our candidates target the earliest pathological events in Alzheimer’s disease and related dementias. This disease-modifying approach offers the potential for meaningful clinical benefit and establishes a new paradigm in neurodegenerative therapeutics.
Multi-cellular Integrated Brain Tissue (miBRAIN) was developed through a collaboration led by Prof. Li-Huei Tsai (MIT), with co-senior authors Prof. Robert Langer and Prof. Joel Blanchard, with key features:
Cellular Completeness: First-in-class integration of all six major brain cell types (neurons, astrocytes, microglia, oligodendrocytes, pericytes, and endothelial cells) derived from donor iPSCs.
3D Architecture: Self-organizing neurovascular units in a brain-mimetic Neuromatrix hydrogel that recapitulate functional synapses, myelination, immune signaling, and blood-brain barrier (BBB) physiology.
Genetic Modularity: Isogenic, editable lines enabling precise APOE4 modeling and patient-specific studies.
Proven Impact: Delivering novel insights into astrocyte-microglia interactions driving tau and amyloid pathology (Stanton et al., PNAS, 2025).
Translational Advantages: Superior relevance compared to rodent models or simplified 2D cultures; scalable for high-content screening, lead and candidate optimization.
Platform Capabilities: High-content screening (HCS) in human APOE4 iPSC-derived neurons, with advanced validation in the miBRAIN 3D system.
Current Progress: Identified druggable targets using our platform, and target validation and lead optimization are underway, supported by non-dilutive NIA/NIH STTR funding.
Next Milestones: Selection of preclinical candidate(s), IND-enabling studies, Strategic partnerships to accelerate clinical development. MCM6 is advancing a portfolio of candidates with the potential to become first-in-class disease-modifying therapies for APOE4-associated Alzheimer’s disease.

Kelvin Lam, Co-Founder. A leading expert in drug discovery, Dr. Lam guides target selection, lead optimization, and preclinical validation for MCM6’s therapeutic programs.
Matthew Stremlau, Co-Founder. A distinguished scientist, Dr. Stremlau leads the strategic translation of APOE4 biology into targeted therapeutics for Alzheimer’s disease and related disorders.
Miranda Yang, Co-Founder. & Assistant Professor. An advisor in platform engineering, Dr. Yang plays a pivotal role in developing and integrating all six major brain cell types into MCM6’s proprietary 3D miBRAIN system and provides strategic scientific guidance.
Joel Blanchard, Advisor & Associate Professor. MCM6 was built upon the foundational scientific contributions of the Blanchard Lab at the Icahn School of Medicine at Mount Sinai. Professor Blanchard continues to provide strategic scientific guidance to the company. MCM6 collaborates closely with world-renowned experts in neuroscience and bioengineering.
MCM6 offers accredited investors a compelling entry point into precision neuroscience, featuring proprietary technology and clear translational objectives: Validated science and a highly human-relevant platform, a focused mechanistic approach targeting the largest genetically defined Alzheimer’s risk group (APOE4 carriers), superior translational models with strong commercial scalability, and advancing toward IND submission with defined capital requirements. We invite qualified investors to partner with MCM6 in transforming the future of Alzheimer’s treatment.
For partnerships, please contact info@mcm6.com
Copyright © 2026 MCM6 - All Rights Reserved.
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.