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Newsroom

Insights and information on our approach to raising awareness of rare diseases, developing new therapies, and supporting our team.

Sienna
Living with ABCC6 Deficiency

  • Scientific Focus
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    • INZ-701
    • Our Pipeline
    • Clinical Trials
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    • Overview
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    • ABCC6 Deficiency
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  • About
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Investigational-Therapy-INZ-701-for-ENPP1-Deficiency-thumb
Investigational Therapy INZ-701 for ENPP1 Deficiency
CheckRare - Madaline Spencer
October 2024
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ENPP1-and-ABCC6-Deficiency-Data-Presented-at-ASBMR-2024-thumb
ENPP1 and ABCC6 Deficiency Data Presented at ASBMR 2024
CheckRare: ENPP1 and ABCC6 Deficiency Data Presented at ASBMR 2024 - Madaline Spencer
October 2024
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US-FDA’s-Rare-Pediatric-Voucher-Program-Faces-Tight-Deadline-For-Reauthorization-thumb
US FDA’s Rare Pediatric Voucher Program Faces Tight Deadline For Reauthorization
Pink Sheet - Sue Sutter
September 2024
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Newsroom thumbnail for Matt Wintons article on BioSpace
Opinion: Congress Must Reauthorize FDA Program for Pediatric Rare Diseases
BioSpace - Matthew Winton
July 2024
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Check Rare Poster
Clinical Trial for ENPP1 and ABCC6 Deficiency
Check Rare - Doug Treco
May 2024
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Check Rare Poster
ENPP1 and ABCC6 Deficiency Overview
Check Rare - Doug Treco
May 2024
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The Power and Potential of GACI Clinical Trials
Figure1 - Podcast Season 10, Episode 2
May 2024
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INZ-701 Trial Update – 2024 PXE Extended Virtual Conference
PXE International - Interview with Yves Sabbagh
March 2024
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State of the Orphan Space
Life Science Leader - Doug Treco Interview
March 2024
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Facilitating Newborn Screening and Early Intervention for Infants Born with Rare Diseases
Catherine Nester byline – Page 25
February 2024
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ENPP1 Deficiency Disorders with Inozyme
DNA Today Podcast - Interview with Yves Sabbagh and Christine O’Brien
January 2024
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Thumbnail for Inozyme Advocate 2023 November
The Inozyme Advocate
Newsletter
November 2023
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Rare Community Profiles: Inozyme’s Catherine Nester Discusses Newborn Screening and the GACI Diagnostic Delay
Catherine Nester Interview
September 2023
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Catherine Nester Discusses the BeginNGS Tool for Newborn Rare Disease Screening Awareness
Catherine Nester Interview
August 2023
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Rady Children’s Institute for Genomic Medicine Launches Phase 2 of BeginNGS Program for Identifying Treatable Genetic Diseases for Newborns
Rady Children’s Press Release
July 2023
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Check Rare Poster
What is ENPP1 Deficiency?
Check Rare - Catherine Nester Interview
February 2023
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Check Rare Poster
The Prevalence of ENPP1 Deficiency
Check Rare - Catherine Nester and Mark Kiel Interview
February 2023
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Dr. Yves Sabbagh – Update on INZ-701 Trial for PXE-2023 – PXE Global Conference
PXE International - Interview with Yves Sabbagh
January 2023
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Hypophosphatemia and the Secret Locked in a Child’s DNA
Figure1 - Podcast Season 6, Episode 3
November 2022
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Mysterious Arterial Calcifications and One of the World’s Most Unique Patients
Figure1 - Podcast Season 6, Episode 1
November 2022
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Rare Disease Report Podcast: Newborn Screening Awareness and Novel Diagnostic Tool
HCP Live – Rare Disease Report Podcast - Interview with Catherine Nester and Dr. Stephen Kingsmore
October 2022
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Wait, How Do You Spell That? A Rare Disease Podcast
GACI Global and Catherine Nester Interview
September 2022
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Advancing Newborn Screening Toward Improving Pediatric Rare Genetic Diseases
Today’s Clinical Lab – Podcast - Interview with Catherine Nester
September 2022
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clinilabs - screen shot of video
Dr. Gary Zammit speaks with Catherine Nester of Inozyme about clinical trials in rare disease
September 2022
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The earlier the better: New consortium leverages infant screening to accelerate treatment
Catherine Nester and Dr. Stephen Kingsmore Interview
July 2022
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Thumbnail for Inozyme Advocate 2022
The Inozyme Advocate
Newsletter
February 2022
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The Inozyme Advocate
Newsletter
November 2020
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The Inozyme Advocate
Newsletter
April 2020
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The Inozyme Advocate
Newsletter
August 2019
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The Inozyme Advocate
Newsletter
December 2018
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321 Summer Street, Suite 400
Boston, MA 02210

INFO@INOZYME.COM
+1 (857) 330-4340

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    • Our Science
    • INZ-701
    • Our Pipeline
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  • Patients and Families
    • Overview
    • ENPP1 Deficiency
    • ABCC6 Deficiency
    • Calciphylaxis
    • Patient Stories
    • Find Your Community
    • Newsroom
  • Healthcare Professionals
    • Overview
    • Genetic Testing
    • Patient Registry
    • Expanded Access
    • Research Support
    • Grants & Sponsorships
  • About
    • Senior Leadership
    • Board of Directors
    • Advisory Boards
    • Expanding Our Reach
    • Contact
  • Life at Inozyme
    • One Energized Team
    • Opportunities
  • Investors
    • Overview
    • Press Releases
    • Events and Presentations
    • Corporate Presentation
    • Financials and SEC Filings
    • Stock Information
    • Analyst Coverage
    • Governance

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