INZ-701 is under clinical development by Inozyme Pharma and currently in Phase II for Rickets. According to GlobalData, Phase II drugs for Rickets have a 50% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how INZ-701’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
INZ-701 overview
INZ-701 is under development for the treatment of rare genetic diseases of ENPP1 deficiency (generalized arterial calcification infancy (GACI) and autosomal recessive hypophosphatemic rickets type II (ARHR2), rare genetic diseases of ABCC6 Deficiency (pseudoxanthoma elasticum or PXE), calciphylaxis, end-stage kidney disease (ESKD) and diseases of neointimal proliferation. It is administered through subcutaneous route.
Inozyme Pharma overview
Inozyme Pharma is a clinical-stage rare disease biopharmaceutical company that develops novel therapeutics for the treatment of rare genetic diseases of ENPP1, ABCC6 deficiencies and impacting the vasculature, soft tissue and skeleton. It is headquartered in Boston, Massachusetts, the US.
For a complete picture of INZ-701’s drug-specific PTSR and LoA scores, buy the report here.
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