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   <title>Voyager gets FDA clearance for first tau gene therapy for Alzheimer's</title>
   <link>http://www.streetinsider.com/Corporate+News/Voyager+gets+FDA+clearance+for+first+tau+gene+therapy+for+Alzheimer%27s/26579588.html</link>
   <description>&lt;p&gt;Voyager Therapeutics Inc. (NASDAQ: VYGR) received U.S. Food and Drug Administration clearance for its Investigational New Drug application for VY1706, a gene therapy targeting tau protein in Alzheimer's disease patients. The company plans to begin dosing adults with early Alzheimer's disease in the second half of 2026.&lt;/p&gt;&lt;p&gt;VY1706 uses a vectorized siRNA that targets MAPT mRNA to reduce both intracellular and extracellular tau levels in the brain. The therapy is delivered through a single intravenous dose using Voyager's TRACER AAV capsid technology, which targets a receptor called ALPL to transport the treatment across the blood-brain barrier.&lt;/p&gt;&lt;p&gt;The upcoming clinical trial will be</description>
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   <pubDate>Mon, 01 Jun 2026 08:01:36 -0400</pubDate>
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   <title>Voyager gets FDA clearance for first tau gene therapy for Alzheimer's</title>
   <link>http://www.streetinsider.com/FDA/Voyager+gets+FDA+clearance+for+first+tau+gene+therapy+for+Alzheimer%27s/26579588.html</link>
   <description>&lt;p&gt;Voyager Therapeutics Inc. (NASDAQ: VYGR) received U.S. Food and Drug Administration clearance for its Investigational New Drug application for VY1706, a gene therapy targeting tau protein in Alzheimer's disease patients. The company plans to begin dosing adults with early Alzheimer's disease in the second half of 2026.&lt;/p&gt;&lt;p&gt;VY1706 uses a vectorized siRNA that targets MAPT mRNA to reduce both intracellular and extracellular tau levels in the brain. The therapy is delivered through a single intravenous dose using Voyager's TRACER AAV capsid technology, which targets a receptor called ALPL to transport the treatment across the blood-brain barrier.&lt;/p&gt;&lt;p&gt;The upcoming clinical trial will be</description>
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   <title>Voyager Receives FDA IND Clearance for VY1706, First Gene Therapy Approach to Reducing Tau Production in the Brain for Alzheimer’s Disease</title>
   <link>http://www.streetinsider.com/Press+Releases/Voyager+Receives+FDA+IND+Clearance+for+VY1706%2C+First+Gene+Therapy+Approach+to+Reducing+Tau+Production+in+the+Brain+for+Alzheimer%E2%80%99s+Disease/26579487.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Dosing of adults with early Alzheimer’s disease in clinical trial expected H2 2026 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Comprehensive preclinical program showed compelling pharmacology and safety profile for VY1706 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- VY1706 uses an IV-delivered, brain-targeted capsid to reduce intracellular and extracellular tau -&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;LEXINGTON, Mass., June  01, 2026  (GLOBE NEWSWIRE) -- Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VY1706, the Company’s investigational gene therapy targeting</description>
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   <title>Voyager Receives FDA IND Clearance for VY1706, First Gene Therapy Approach to Reducing Tau Production in the Brain for Alzheimer’s Disease</title>
   <link>http://www.streetinsider.com/Press+Releases/Voyager+Receives+FDA+IND+Clearance+for+VY1706%2C+First+Gene+Therapy+Approach+to+Reducing+Tau+Production+in+the+Brain+for+Alzheimer%E2%80%99s+Disease/26579487.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Dosing of adults with early Alzheimer’s disease in clinical trial expected H2 2026 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Comprehensive preclinical program showed compelling pharmacology and safety profile for VY1706 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- VY1706 uses an IV-delivered, brain-targeted capsid to reduce intracellular and extracellular tau -&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;LEXINGTON, Mass., June  01, 2026  (GLOBE NEWSWIRE) -- Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VY1706, the Company’s investigational gene therapy targeting</description>
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   <title>Voyager Receives FDA IND Clearance for VY1706, First Gene Therapy Approach to Reducing Tau Production in the Brain for Alzheimer’s Disease</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Dosing of adults with early Alzheimer’s disease in clinical trial expected H2 2026 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Comprehensive preclinical program showed compelling pharmacology and safety profile for VY1706 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- VY1706 uses an IV-delivered, brain-targeted capsid to reduce intracellular and extracellular tau -&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;LEXINGTON, Mass., June  01, 2026  (GLOBE NEWSWIRE) -- Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VY1706, the Company’s investigational gene therapy targeting</description>
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   <title>Voyager Receives FDA IND Clearance for VY1706, First Gene Therapy Approach to Reducing Tau Production in the Brain for Alzheimer’s Disease</title>
   <link>http://www.streetinsider.com/Press+Releases/Voyager+Receives+FDA+IND+Clearance+for+VY1706%2C+First+Gene+Therapy+Approach+to+Reducing+Tau+Production+in+the+Brain+for+Alzheimer%E2%80%99s+Disease/26579487.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Dosing of adults with early Alzheimer’s disease in clinical trial expected H2 2026 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Comprehensive preclinical program showed compelling pharmacology and safety profile for VY1706 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- VY1706 uses an IV-delivered, brain-targeted capsid to reduce intracellular and extracellular tau -&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;LEXINGTON, Mass., June  01, 2026  (GLOBE NEWSWIRE) -- Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VY1706, the Company’s investigational gene therapy targeting</description>
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   <title>Voyager Receives FDA IND Clearance for VY1706, First Gene Therapy Approach to Reducing Tau Production in the Brain for Alzheimer’s Disease</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Voyager+Receives+FDA+IND+Clearance+for+VY1706%2C+First+Gene+Therapy+Approach+to+Reducing+Tau+Production+in+the+Brain+for+Alzheimer%E2%80%99s+Disease/26579487.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Dosing of adults with early Alzheimer’s disease in clinical trial expected H2 2026 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Comprehensive preclinical program showed compelling pharmacology and safety profile for VY1706 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- VY1706 uses an IV-delivered, brain-targeted capsid to reduce intracellular and extracellular tau -&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;LEXINGTON, Mass., June  01, 2026  (GLOBE NEWSWIRE) -- Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VY1706, the Company’s investigational gene therapy targeting</description>
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   <title>Voyager Receives FDA IND Clearance for VY1706, First Gene Therapy Approach to Reducing Tau Production in the Brain for Alzheimer’s Disease</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Voyager+Receives+FDA+IND+Clearance+for+VY1706%2C+First+Gene+Therapy+Approach+to+Reducing+Tau+Production+in+the+Brain+for+Alzheimer%E2%80%99s+Disease/26579487.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Dosing of adults with early Alzheimer’s disease in clinical trial expected H2 2026 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Comprehensive preclinical program showed compelling pharmacology and safety profile for VY1706 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- VY1706 uses an IV-delivered, brain-targeted capsid to reduce intracellular and extracellular tau -&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;LEXINGTON, Mass., June  01, 2026  (GLOBE NEWSWIRE) -- Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VY1706, the Company’s investigational gene therapy targeting</description>
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   <title>Voyager Receives FDA IND Clearance for VY1706, First Gene Therapy Approach to Reducing Tau Production in the Brain for Alzheimer’s Disease</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Voyager+Receives+FDA+IND+Clearance+for+VY1706%2C+First+Gene+Therapy+Approach+to+Reducing+Tau+Production+in+the+Brain+for+Alzheimer%E2%80%99s+Disease/26579487.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Dosing of adults with early Alzheimer’s disease in clinical trial expected H2 2026 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Comprehensive preclinical program showed compelling pharmacology and safety profile for VY1706 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- VY1706 uses an IV-delivered, brain-targeted capsid to reduce intracellular and extracellular tau -&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;LEXINGTON, Mass., June  01, 2026  (GLOBE NEWSWIRE) -- Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VY1706, the Company’s investigational gene therapy targeting</description>
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   <title>Voyager Receives FDA IND Clearance for VY1706, First Gene Therapy Approach to Reducing Tau Production in the Brain for Alzheimer’s Disease</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Voyager+Receives+FDA+IND+Clearance+for+VY1706%2C+First+Gene+Therapy+Approach+to+Reducing+Tau+Production+in+the+Brain+for+Alzheimer%E2%80%99s+Disease/26579487.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Dosing of adults with early Alzheimer’s disease in clinical trial expected H2 2026 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- Comprehensive preclinical program showed compelling pharmacology and safety profile for VY1706 -&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;- VY1706 uses an IV-delivered, brain-targeted capsid to reduce intracellular and extracellular tau -&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;LEXINGTON, Mass., June  01, 2026  (GLOBE NEWSWIRE) -- Voyager Therapeutics, Inc. (Nasdaq: VYGR), a biotechnology company dedicated to leveraging genetics to treat neurological diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VY1706, the Company’s investigational gene therapy targeting</description>
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   <title>Form  8-K        Voyager Therapeutics,     For: Jun 01</title>
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   <title>Form  8-K        Voyager Therapeutics,     For: Jun 01</title>
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   <pubDate>Mon, 01 Jun 2026 08:00:00 -0400</pubDate>
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   <title>H.C. Wainwright Reiterates Buy Rating on Voyager Therapeutics (VYGR)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/H.C.+Wainwright+Reiterates+Buy+Rating+on+Voyager+Therapeutics+%28VYGR%29/26545588.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Patrick R. Trucchio reiterated a Buy rating and $25.00 price target on Voyager Therapeutics (NASDAQ: VYGR).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;Voyager started 2026 with clear pipeline momentum including the completion of a key investigational new drug (IND)-enabling good laboratory practice (GLP) toxicology study for its wholly-owned VY1706 program—a one-time intravenously (IV) administered tau-silencing gene therapy in Alzheimer’s disease — positioning an IND filing on-track for 2Q26, with a potential first-in-human study start in 2H26. The data from the VY1706 GLP tox study were presented by Chief Scientific Officer Todd Carter, Ph.D., in a late-breaking oral presentation at the American</description>
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   <pubDate>Tue, 26 May 2026 06:58:34 -0400</pubDate>
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   <title>Form  3          Voyager Therapeutics,     For: May 08  Filed by: Quinlan Amy</title>
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   <pubDate>Mon, 18 May 2026 16:01:00 -0400</pubDate>
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   <title>Form  3          Voyager Therapeutics,     For: May 08  Filed by: Quinlan Amy</title>
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   <pubDate>Mon, 18 May 2026 16:01:00 -0400</pubDate>
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   <title>Form  144        Voyager Therapeutics,                  Filed by: Jorgensen Nathan D.</title>
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   <title>Form  144        Voyager Therapeutics,                  Filed by: Jorgensen Nathan D.</title>
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   <title>Form  SCHEDULE 13G/A  Voyager Therapeutics,                  Filed by: EcoR1 Capital, LLC</title>
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   <title>Form  SCHEDULE 13G/A  Voyager Therapeutics,                  Filed by: EcoR1 Capital, LLC</title>
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   <title>Form  SCHEDULE 13G/A  Voyager Therapeutics,                  Filed by: ARMISTICE CAPITAL, LLC</title>
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   <title>Form  SCHEDULE 13G/A  Voyager Therapeutics,                  Filed by: ARMISTICE CAPITAL, LLC</title>
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   <title>Form  144        Voyager Therapeutics,                  Filed by: Jorgensen Nathan D.</title>
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   <pubDate>Fri, 15 May 2026 10:35:00 -0400</pubDate>
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   <title>Form  144        Voyager Therapeutics,                  Filed by: Jorgensen Nathan D.</title>
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   <title>Voyager presents positive safety data for Alzheimer's gene therapy VY1706</title>
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   <description>&lt;p&gt;Voyager Therapeutics Inc. (NASDAQ: VYGR) reported positive three-month toxicology data for VY1706, its investigational tau silencing gene therapy for Alzheimer's disease, at the American Society of Gene &amp; Cell Therapy's 2026 Annual Meeting in Boston.&lt;/p&gt;&lt;p&gt;The study showed VY1706 was well tolerated with no adverse clinical pathology or histopathological findings up to the highest dose tested of 5E13 vg/kg in non-human primates. The single intravenous dose reduced tau protein by up to 64% in key brain regions at 13 weeks following treatment.&lt;/p&gt;&lt;p&gt;The company's FDA investigational new drug application process for VY1706 remains on track for the second quarter of 2026, with</description>
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   <pubDate>Wed, 13 May 2026 06:02:27 -0400</pubDate>
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   <title>Voyager presents positive safety data for Alzheimer's gene therapy VY1706</title>
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   <description>&lt;p&gt;Voyager Therapeutics Inc. (NASDAQ: VYGR) reported positive three-month toxicology data for VY1706, its investigational tau silencing gene therapy for Alzheimer's disease, at the American Society of Gene &amp; Cell Therapy's 2026 Annual Meeting in Boston.&lt;/p&gt;&lt;p&gt;The study showed VY1706 was well tolerated with no adverse clinical pathology or histopathological findings up to the highest dose tested of 5E13 vg/kg in non-human primates. The single intravenous dose reduced tau protein by up to 64% in key brain regions at 13 weeks following treatment.&lt;/p&gt;&lt;p&gt;The company's FDA investigational new drug application process for VY1706 remains on track for the second quarter of 2026, with</description>
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