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Voyager Therapeutics develops genetic medicines for neurological diseases. Its focus is on delivering therapeutic genes to the brain by using a proprietary AAV (adeno-associated virus) capsid discovery platform that enables intravenous delivery across the blood-brain barrier. This allows targeted treatment for conditions like ALS and other central nervous system disorders. The company works mainly through research and development, forming partnerships and licensing deals with larger pharmaceutical companies to fund and accelerate bringing therapies to patients. Unlike many biotech firms that rely on a single approach, Voyager emphasizes a platform-based strategy to improve brain delivery and collaborates with partners to advance candidates through development and potentially to market. The overarching goal is to create meaningful, disease-modifying genetic medicines that can reach the brain and improve outcomes for people with neurological diseases.
Industries
Biotechnology
Healthcare
Company Size
51-200
Company Stage
IPO
Headquarters
Cambridge, Massachusetts
Founded
2014
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Total Funding
$460.5M
Above
Industry Average
Funded Over
6 Rounds
Flexible Work Hours
Voyager Therapeutics, a clinical-stage gene therapy company, received qualified endorsement from Jim Cramer for a 23-year-old caller based solely on time horizon. The stock has fallen 69% over ten years, and Cramer warned it "may take a lifetime" to become profitable. The Cambridge-based firm reported Q1 revenue of $2.59 million, missing consensus by 70% and falling 60% year-over-year. Net loss reached $27.94 million. Despite having no approved products and a market capitalisation of $213.6 million, analysts give 11 Buy ratings with a $15 average target—nearly four times its $3.50 price—driven by 2026 Alzheimer's trial dosing. With a 240-million-share authorisation, recent CFO resignation and beta above 1.25, Voyager remains a high-volatility bet.
Voyager's tau-targeted gene therapy VY1706 for Alzheimer's disease to be featured in Developing Topics poster presentation at AAIC 2026. GlobeNewswire | Voyager Therapeutics, Inc. Today at 5:01am PDT LEXINGTON, Mass., June 29, 2026 (GLOBE NEWSWIRE) - Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced a Developing Topics (late-breaking) poster presentation at the upcoming Alzheimer's Association International Conference (AAIC) taking place in London, July 12-15, 2026. The Developing Topics poster presentation will feature VY1706, Voyager's investigational gene therapy targeting intracellular and extracellular tau for Alzheimer's disease (AD). Earlier this month, Voyager received U.S. Food and Drug Administration (FDA) Investigational New Drug (IND) clearance for VY1706, enabling initiation of a clinical trial in adults with early AD, with dosing expected to begin in the second half of the year. Developing Topics: Drug Development IND-enabling GLP NHP study of VY1706, a BBB-crossing AAV gene therapy targeting tau in Alzheimer's (#Monday-1207). Rajeev Sivasankaran, SVP, Neuroscience, and Vik Arora, VP, Toxicology. Monday, July 13, 2026, 7:30 a.m. - 4:15 p.m. GMT The Developing Topics poster presentation will be available on Voyager's website at: https://www.voyagertherapeutics.com/science-publications. About VY1706 VY1706 is an investigational gene therapy for Alzheimer's disease (AD) that targets tau, a protein associated with neurodegeneration and cognitive decline in AD. The core of VY1706 is a potent, vectorized siRNA that targets MAPT mRNA to decrease levels of both intracellular and extracellular tau in the brain. This core is encapsulated in a Voyager TRACER(TM) AAV capsid that leverages ALPL, a well-conserved, novel receptor identified by Voyager, to deliver the siRNA into the brain following a one-time, intravenous (IV) dose. The efficacy and safety of VY1706 have been assessed in a comprehensive preclinical program spanning multiple species. Three-month good laboratory practice (GLP) toxicology data for VY1706 demonstrated a favorable tolerability profile with no adverse clinical pathology or histopathological findings up to the highest dose tested (5E13 vg/kg) following a single IV dose in non-human primates (NHPs). VY1706 has also been demonstrated to reduce tau protein up to 75% in key NHP brain regions relevant to AD and to de-target the liver, a source of adverse events associated with other systemically administered gene therapies. Voyager is initiating a clinical trial of VY1706 administered as a one-time IV dose to adults with early AD. About Voyager Therapeutics Voyager Therapeutics, Inc. (Nasdaq: VYGR) is a biotechnology company dedicated to leveraging the power of human genetics to modify the course of - and ultimately cure - neurological diseases. Its pipeline includes programs for Alzheimer's disease, Friedreich's ataxia, Parkinson's disease, amyotrophic lateral sclerosis (ALS), and multiple other diseases of the central nervous system. Many of its programs are derived from its TRACER(TM) AAV capsid discovery platform, which eNews Park Forest, Inc. has used to generate novel capsids and identify associated receptors to potentially enable high brain penetration with genetic medicines following intravenous dosing. Some of its programs are wholly owned, and some are advancing with partners including Alexion, AstraZeneca Rare Disease; Novartis Pharma AG; and Neurocrine Biosciences, Inc. For more information, visit http://www.voyagertherapeutics.com. Voyager Therapeutics(R) is a registered trademark, and TRACER(TM) and Voyager NeuroShuttle(TM) are trademarks, of Voyager Therapeutics, Inc. Forward-Looking Statements This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995 and other federal securities laws, including, without limitation, implied and express statements about Voyager's beliefs and expectations regarding Voyager's advancement of the VY1706 program, including the timing and achievement of clinical development milestones such as Voyager's intentions to initiate clinical trials, clinical trial enrollment, and achievement of first-in-human dosing in AD in the second half of 2026; the therapeutic potential, clinical benefit, safety and pharmacological effect of VY1706; Voyager's ability to execute across its pipeline and platforms; and the mission and goals for Voyager's business. The use of words such as "may," "will," "might," "would," "could," "should," "expect," "plan," "anticipate," "believe," "potential," "intend," "seek," "predict," "estimate," "project," "target," or "continue" and other similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. All forward-looking statements are based on management's current estimates and assumptions and are subject to a number of risks, uncertainties, and important factors that may cause actual results to differ materially from any forward-looking statements in this press release. Factors include, among others, the risks and uncertainties inherent in the development of product candidates, including the initiation, enrollment, timing, cost, progress, and results of Voyager's planned and future clinical trials; expectations and decisions of regulatory authorities; Voyager's ability to replicate positive results from earlier preclinical studies or clinical trials in current or future clinical trials; potential adverse events Voyager may encounter that could negatively impact development; outcomes of third-party preclinical studies and clinical trials that could impact Voyager's development plans; Voyager's ability to demonstrate that current or future product candidates are safe and effective for their proposed indications; Voyager's scientific approach and continued development of its technology platforms, including the TRACER and non-viral discovery platforms; the development by third parties of capsid or non-viral identification platforms that may be competitive to its platforms and programs; Voyager's ability to create and protect its intellectual property rights; the progress and success of programs under current or future collaboration and license agreements; the sufficiency of Voyager's cash resources to fund its operations and pursue its corporate objectives; and technical and other unexpected hurdles in the development, manufacture and supply of Voyager's product candidates, may delay its timing, change its plans, increase its costs, or otherwise negatively impact its business or the sufficiency of its cash resources to fund operations. These risks and uncertainties are described in Voyager's most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission as updated by its subsequent filings with the Securities and Exchange Commission. All information in this press release is as of today's date, and any forward-looking statement speaks only as of the date on which it was made. Voyager undertakes no obligation to publicly update or revise this information or any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law. Contacts Company and Investors: Trista Morrison, NACD.DC, [email protected] Media: Lisa Guiterman, [email protected] This is a paid placement. For further inquiries, please contact GlobeNewswire directly.
Voyager to present at H.C. Wainwright 7th Annual Neuro Perspectives Hybrid Conference. LEXINGTON, Mass., June 11, 2026 (GLOBE NEWSWIRE) - Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that Alfred W. Sandrock, Jr., M.D., Ph.D., Chief Executive Officer of Voyager, will participate in a pre-recorded fireside chat at the H.C. Wainwright 7th Annual Neuro Perspectives Hybrid Conference. An on-demand webcast of the pre-recorded fireside chat will be available and may be accessed from the Investors section of Voyager's website at ir.voyagertherapeutics.com starting at 7:00 a.m. ET on June 15, 2026. The on-demand webcast will be archived on the Company's website for at least 30 days. About Voyager Therapeutics Voyager Therapeutics, Inc. (Nasdaq: VYGR) is a biotechnology company dedicated to leveraging the power of human genetics to modify the course of - and ultimately cure - neurological diseases. Our pipeline includes programs for Alzheimer's disease, Friedreich's ataxia, Parkinson's disease, amyotrophic lateral sclerosis (ALS), and multiple other diseases of the central nervous system. Many of our programs are derived from our TRACER(TM) AAV capsid discovery platform, which we have used to generate novel capsids and identify associated receptors to potentially enable high brain penetration with genetic medicines following intravenous dosing. Some of our programs are wholly owned, and some are advancing with partners including Alexion, AstraZeneca Rare Disease; Novartis Pharma AG; and Neurocrine Biosciences, Inc. For more information, visit http://www.voyagertherapeutics.com. Voyager Therapeutics(R) is a registered trademark, and TRACER(TM) and Voyager NeuroShuttle(TM) are trademarks, of Voyager Therapeutics, Inc. Contacts Trista Morrison, NACD.DC, [email protected] Investors: Sarah McCabe, [email protected] Media: Lisa Guiterman, [email protected] Company Profile Voyager Therapeutics, Inc. Industry: Biotechnology Website: https://voyagertherapeutics.com Recommended reading.
Voyager Therapeutics had cash reserves of $141 million as of March 2026, giving it a cash runway of approximately 13 months based on its annual cash burn of $130 million. The biotechnology company increased its cash burn by 14% year-on-year whilst operating revenue declined 45% during the same period. The pre-revenue company faces concerns about its ability to sustain operations without raising additional capital. Voyager Therapeutics carried zero debt on its March 2026 balance sheet. The convergence of rising cash burn and declining revenue raises questions about the company's need to secure additional funding through equity issuance or debt to support future operations. The Series C round was led by Ribbit Capital, with participation from Sequoia and Kleiner Perkins.
Voyager Therapeutics has received FDA clearance for its Investigational New Drug application for VY1706, the first gene therapy targeting tau production in Alzheimer's disease. Dosing in adults with early Alzheimer's is expected to begin in the second half of 2026. VY1706 uses an intravenously delivered, brain-targeted capsid containing vectorised siRNA to reduce intracellular and extracellular tau protein. Preclinical studies demonstrated tau protein reductions of up to 75% in key brain regions, whilst avoiding liver-related adverse events associated with other systemic gene therapies. The multi-site, open-label trial will enrol up to 18 patients with early Alzheimer's across three dose-escalation cohorts. The primary endpoint evaluates safety and tolerability, whilst secondary endpoints assess tau biomarkers in cerebrospinal fluid and changes in tau pathology via PET imaging.
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Industries
Biotechnology
Healthcare
Company Size
51-200
Company Stage
IPO
Headquarters
Cambridge, Massachusetts
Founded
2014
Find jobs on Simplify and start your career today