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CONTACT US



Home

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For HCPs

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Contact Us
Theme




BREAKTHROUGH SOLUTIONS AT THE SPEED OF SCIENCE


COMMITTED TO RESTORING HEALTH AND HOPE TO PATIENTS WITH DISEASES OF ABNORMAL
MINERALIZATION

See How we help

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WHAT MAKES


US DIFFERENT


OUR PEOPLE.


COLLABORATION IS THE CORE OF WHAT WE DO. DRIVEN BY EMPATHY, COMPASSION AND
TIRELESS INNOVATION, INOZYME PHARMA BRINGS TOGETHER LEADING TALENT TO CREATE
LIFE-SAVING THERAPIES FOR PATIENTS AND THEIR FAMILIES.

Help us deliver hope


OUR SCIENCE


INOZYME IS DEVELOPING OPTIONS WHERE NONE EXIST, TO TREAT RARE DISEASES OF
ABNORMAL MINERALIZATION.

See What We're developing


PATIENTS & HEALTH


CARE PROVIDERS


PEOPLE WITH RARE MINERALIZATION DISORDERS DESERVE EFFECTIVE THERAPIES. WE’RE
PARTNERING WITH PATIENTS, THEIR FAMILIES, AND THEIR HEALTH CARE PROVIDERS TO
ADVANCE LIFE-CHANGING THERAPEUTIC SOLUTIONS AND SAVE LIVES.

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PATIENTS



HEALTHCARE PROVIDERS



INVESTORS


RARE PATIENTS.


 RARE  SOLUTIONS.


INZ-701 



INOZYME PHARMA IS FILLING UNMET MEDICAL NEEDS BY DEVELOPING A TARGETED TREATMENT
FOR PATIENTS SUFFERING FROM RARE DISEASES OF  ABNORMAL MINERALIZATION.


01

INZ-701 INCREASES INORGANIC PYROPHOSPHATE (PPI) AND ADENOSINE LEVELS BY CLEAVING
EXTRACELLULAR ATP THROUGHOUT THE BODY – MIMICKING THE FUNCTION OF THE
MEMBRANE-BOUND ENPP1 PROTEIN.

02

INZ-701 IS FORMULATED FOR SUBCUTANEOUS DELIVERY AND DESIGNED TO HAVE PROLONGED
EXPOSURE AND ELIMINATION PHASES, MAKING DOSING POSSIBLE AT INFREQUENT INTERVALS.

03

INZ-701 IS A NOVEL ERT THAT CAN TARGET GENETIC AND NON-GENETIC DISEASES WHICH
INVOLVE LOW LEVELS OF PPI AND ADENOSINE – INCLUDING ENPP1 DEFICIENCY, ABCC6
DEFICIENCY AND CALCIPHYLAXIS.

See Our solution


JOIN A CLINICAL TRIAL

YOU ARE PART OF THE SOLUTION.

We are enrolling adult patients with ENPP1 Deficiency or ABCC6 Deficiency (PXE)
in the first clinical trials for a potential new treatment. With your
participation, we can better understand this disease and help inform possible
future treatment options.

Join a clinical Trial
Inozyme is a global leader in developing therapies for rare mineralization
disorders
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