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VOYAGER DIGITAL LT

VOYAGER DIGITAL LT logo
🇺🇸United States
Ownership
Public
Established
2014-01-01
Employees
162
Market Cap
$361.5M
Website
http://www.voyagertherapeutics.com
Introduction

Voyager Therapeutics, Inc. is a clinical-stage gene therapy company, which engages in the development of treatments for severe neurological diseases. Its pipeline of gene therapy programs includes VY-AADC, VY-SOD101, VY-HTT01, VY-FXN01, Tau Program, and VY-NAV01. The company was founded by Guang Ping Gao, Mark A. Kay, Krystof Bankiewicz, and Phillip Zamore in June 2013 and is headquartered in Lexington, MA.

Clinical Trials

2

Active:0
Completed:0

Trial Phases

1 Phases

Phase 1:2

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials

Phase 1
2 (100.0%)

VY7523-102: Randomized, Placebo-Controlled, Double-Blind, Multiple Ascending Dose Study in Participants With Early Alzheimer's Disease

Phase 1
Recruiting
Conditions
Alzheimer's Disease (AD)
Interventions
Drug: Placebo Comparator
First Posted Date
2025-03-13
Last Posted Date
2025-07-23
Lead Sponsor
Voyager Therapeutics
Target Recruit Count
52
Registration Number
NCT06874621
Locations
🇺🇸

VYGR Site 840018, Los Angeles, California, United States

🇺🇸

VYGR Site 840016, Orange, California, United States

🇺🇸

VYGR Site 840022, San Francisco, California, United States

and more 20 locations

Safety and Tolerability Study With VY-HTT01, in Adults With Early Manifesting Huntington's Disease

Phase 1
Withdrawn
Conditions
Huntington Disease
First Posted Date
2021-05-13
Last Posted Date
2021-08-16
Lead Sponsor
Voyager Therapeutics
Registration Number
NCT04885114

News

Voyager Therapeutics Advances Novel APOE4 Gene Therapy for Alzheimer's Disease Using IV-Delivered TRACER Platform

Voyager Therapeutics has launched a new gene therapy program targeting APOE4, the strongest genetic risk factor for Alzheimer's disease, using its proprietary TRACER capsid technology for intravenous delivery.

Vima Therapeutics Emerges with $60M to Develop First Oral Therapy for Dystonia

Vima Therapeutics launched with $60 million Series A funding led by Atlas Venture to advance VIM0423, a potential first-in-class oral therapy for dystonia targeting muscarinic cholinergic receptors.

Voyager Therapeutics Publishes Breakthrough Research on ALPL-Mediated Blood-Brain Barrier Transport for Gene Therapy

Voyager Therapeutics published the first peer-reviewed study demonstrating alkaline phosphatase (ALPL) receptor's ability to transport novel AAV capsids across the blood-brain barrier in Molecular Therapy.

Voyager Therapeutics Redirects SOD1 ALS Gene Therapy Development After Preclinical Findings

Voyager Therapeutics announces strategic shift in their SOD1 ALS gene therapy program after three-month non-human primate data indicated the need for alternate payload evaluation.

Bayer's Cell and Gene Therapy Programs for Parkinson's Disease Enter Clinical Trials

• Bayer's BlueRock Therapeutics initiated a Phase 1 trial of DA01, a cell-based therapy using stem cell-derived dopaminergic neurons, to replenish lost neurons in Parkinson's patients. • AskBio, another Bayer subsidiary, has begun a Phase 1b trial of its gene therapy for Parkinson's, aiming to halt or reverse motor control decline by delivering a gene for glial cell line-derived neurotrophic factor (GDNF). • The FDA granted fast-track review to BlueRock's DA01, potentially accelerating its development through increased communication with the regulator and a shorter review period. • These trials mark a significant step in Bayer's strategy to develop cell and gene therapies that could regenerate dopamine-producing neurons, addressing a major unmet need in Parkinson's disease.

Gene and Cell Therapies Show Promise in Treating CNS Disorders

The market for gene and cell therapies targeting CNS disorders was valued at approximately USD 1 billion in 2021 and is projected to grow significantly by 2034.

OrsoBio Secures $67M for Obesity Drugs, Vor Bio's AML Therapy Shows Promise, and More

OrsoBio, backed by Eli Lilly, raised $67 million to advance its portfolio of weight loss medicines targeting different mechanisms than GLP-1 therapies.

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