Pipeline

Advancing transformative medicines
for neurological diseases.

 

Neurologic diseases – which are estimated to impact more than 1 billion people globally – represent a significant burden on those who suffer from them, on their families and communities, and on the healthcare system.

Thanks to significant advances in human genetics and genomics, we now understand the molecular causes of many neurological diseases and know how to target them.

Our pipeline includes medicines targeting the genetics underlying multiple neurological diseases.

INDICATION / MECHANISM

Early Research

Late Research

IND-Enabling

WHOLLY-OWNED

+ ALZHEIMER’S DISEASE / Anti-tau Antibody (VY-TAU01)

+ ALZHEIMER’S EARLY RESEARCH / Two Gene Therapy Programs

+ ALS / SOD1 Gene Therapy (Gene Silencing)

OTHER EARLY RESEARCH / Two Gene Therapy Programs

REIMBURSED

PARKINSON’S & OTHERS / GBA1 Gene Therapy (Gene Replacement)
Neurocrine Collaboration (VYGR has 50% cost/profit split option)

FRIEDREICH’S ATAXIA / FXN Gene Therapy (Gene Replacement)
Neurocrine Collaboration (VYGR has 40% cost/profit split option)

UNDISCLOSED DISEASES / Five Gene Therapy Programs
Neurocrine Collaboration

Undisclosed

LICENSED

RARE NEUROLOGICAL DISEASE / Gene Therapy

Alexion, AstraZeneca Rare Disease License

CNS DISEASES / Two Gene Therapy Programs

Novartis License

PRION DISEASE / Gene Therapy

Sangamo License

One of the most significant challenges in neurotherapeutics remains developing medicines that can cross the blood-brain barrier and hit their targets. To address this problem, Voyager has discovered novel capsids and identified associated receptors that potentially enable exceptional delivery across the blood-brain barrier following intravenous dosing.

Patient Resources

One of Voyager’s core values is “Patients First.” This means we act with urgency and drive every decision with the knowledge that patients are waiting for us.

Partners

Our allies in realizing the potential of neurogenetic medicines