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Inozyme Pharma Reports Third Quarter 2023 Financial Results and Provides Business Highlights

– Patient recruitment underway in ENERGY-3 Pivotal Trial of INZ-701 in pediatric patients with ENPP1 Deficiency; topline data expected mid-2025 –

United statesStefan rileyDouglasa trecoInozyme pharmaMatt peraPamerican society for boneDrug administrationInozyme pharma incDevelopment rd expensesAmerican society for nephrologyPaediatric committee of the european medicines agencyMineral researchCorporate communicationsAmerican society of nephrology kidney weekExchange commissionAmerican society

Inozyme Pharma Highlights Inclusion of Generalized Arterial Calcification of Infancy (GACI) in Genomics England s Generation Study of Rare Conditions

Inozyme Pharma Highlights Inclusion of Generalized Arterial Calcification of Infancy (GACI) in Genomics England s Generation Study of Rare Conditions
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Inozyme Pharma Highlights Inclusion of Generalized Arterial Calcification of Infancy (GACI) in Genomics England s Generation Study of Rare Conditions -October 10, 2023 at 08:31 am EDT

BOSTON, Oct. 10, 2023 Inozyme Pharma, Inc. , a clinical-stage rare disease biopharmaceutical company developing novel therapeutics for the treatment of pathologic mineralization and intimal.

United kingdomUnited statesInozyme pharmaCatherine nesterStefan rileyMatt peraExchange commissionUnited kingdom national health serviceCorporate communicationsInozyme pharma incGlobenewswire incGeneralized arterial calcificationGenomic englandNational health serviceGenomics englandGeneration study

Inozyme Raises $73 Million to Advance Pipeline Targeting Rare Diseases of Abnormal Mineralization

Inozyme Raises $73 Million to Advance Pipeline Targeting Rare Diseases of Abnormal Mineralization
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Inozyme pharmaGeneralized arterial calcification

The Balancing Act® on Lifetime to Feature ENPP1 Deficiency

The Balancing Act® on Lifetime to Feature ENPP1 Deficiency Educational Episode to Highlight Symptoms of ENPP1 Deficiency and the Importance of Early Diagnosis BOSTON, March 11, 2021 (GLOBE NEWSWIRE) Inozyme Pharma, Inc., a rare disease biopharmaceutical company developing novel therapeutics for the treatment of disorders of abnormal mineralization, announced today that ENPP1 deficiency will be featured on The Balancing Act ® as part of the show’s recurring “Behind the Mystery of Rare and Genetic Diseases” series to raise awareness for this rare, debilitating, and life-threatening mineralization disease for which there are currently no approved treatment options. The episode will feature Janine Hicks, a patient living with ENPP1 deficiency; her parents, Donna and Peter Hicks; and Professor Zulf Mughal, a treating physician and researcher and Consultant in Pediatric Bone Disorders, Royal Manchester Children’s Hospital, Manchester University NHS Foundation Trust. The se

United statesPeter hicksInozyme pharmaChristine obrienJoseph schlessingerAlex van reesZulf mughalAxel bolteJanine hicksLiz molloyDemetrios braddockExchange commissionYale universityManchester universityInozyme pharma incEducational episode

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