Pixatimod is under clinical development by Zucero Therapeutics and currently in Phase II for Metastatic Melanoma. According to GlobalData, Phase II drugs for Metastatic Melanoma have a 36% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Pixatimod’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.
Pixatimod overview
Zucero Therapeutics overview
Zucero Therapeutics formerly Zucero Therapeutics Pty Ltd is a biotechnology company, which strives to discover and develop modified sugar compounds for the treatment of cancer. Its pipeline product candidate, PG545 (pixatimod, pINN), a new immunomodulatory agent, stimulates myeloid cells (M1 macrophages and dendritic cells (DC)). Initially, it stimulates the DC, leading to the activation of natural killer (NK) cells that are capable of destroying lymphomas. Next, it blocks tumour-associated macrophages (TAMs), in mouse models, which causes the inhibition of heparanase. PG545 completed a phase Ia clinical trial as a monotherapy in solid tumors and other inflammatory conditions. The company has research office in Darra, Queensland, Australia. Zucero Therapeutics is headquartered in Geelong, Victoria, Australia.
For a complete picture of Pixatimod’s drug-specific PTSR and LoA scores, buy the report here.
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