MARKET

VYGR

VYGR

Voyager Therapeutics Inc
NASDAQ
9.19
+0.29
+3.26%
Closed 17:00 07/25 EDT
OPEN
8.93
PREV CLOSE
8.90
HIGH
9.28
LOW
8.86
VOLUME
431.76K
TURNOVER
0
52 WEEK HIGH
11.72
52 WEEK LOW
6.06
MARKET CAP
499.88M
P/E (TTM)
-50.6895
1D
5D
1M
3M
1Y
5Y
1D
Sangamo Therapeutics: A Bust Or Billion Dollar Valuation In The Remaking
Seeking Alpha · 3d ago
VOYAGER THERAPEUTICS ANNOUNCES INDUCEMENT GRANTS UNDER NASDAQ LISTING RULE 5635(C)(4)
Reuters · 3d ago
Weekly Report: what happened at VYGR last week (0715-0719)?
Weekly Report · 4d ago
Lexeo stock drops 24% amid Friedreich Ataxia study results
Lexeo Therapeutics reported interim Phase 1/2 clinical data for its drug LX2006 for the treatment of Friedreich Ataxia, or FA, cardiomyopathy. The company plans to explore expedited development for the drug. There are currently no approved treatments for FA.
Seeking Alpha · 07/15 16:03
Weekly Report: what happened at VYGR last week (0708-0712)?
Weekly Report · 07/15 09:17
Insider Sales At Voyager Therapeutics Landed A Good Price
President Alfred Sandrock made the biggest insider sale in the last year at Voyager Therapeutics, Inc. (NASDAQ:VYGR) The company has seen no insider purchases over the past year. Our data suggests the insider sale of shares was at a higher price than the current share price. VoyagerTherapeutics insiders own 1.1% of the company. But the company may not be the best stock to buy.
Simply Wall St · 07/12 19:38
VOYAGER THERAPEUTICS ANNOUNCES INDUCEMENT GRANTS UNDER NASDAQ LISTING RULE 5635(C)(4)
Reuters · 07/09 20:01
Neurocrine's Pipeline, Including Crinecerfont's Priority Review, Drives Long-Term Growth
Seeking Alpha · 07/09 14:32
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About VYGR
Voyager Therapeutics, Inc. is a biotechnology company focused on advancing neurogenetic medicines. The Company’s pipeline includes programs for Alzheimer’s disease, amyotrophic lateral sclerosis (ALS), Parkinson’s disease, and multiple other diseases of the central nervous system. Many of its programs are derived from its TRACER AAV capsid discovery platform, which is used to generate novel capsids and identify associated receptors to potentially enable high brain penetration with genetic medicines following intravenous dosing. Its pipeline of programs, all of which are in preclinical development, include Anti-Tau Antibody (VY-TAU01), SOD1 Silencing Gene Therapy Program, Tau Silencing Gene Therapy Program, Vectorized Anti-Amyloid Antibody Early Research Program, Friedreich’s Ataxia Program: VY-FXN01, GBA1 Gene Replacement Program, HD Program, and others. VY-TAU01 is for the treatment of Alzheimer’s disease. SOD1 Silencing Gene Therapy Program is for the treatment of ALS.

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