EO-2002 is under clinical development by Emmecell and currently in Phase I for Corneal Edema. According to GlobalData, Phase I drugs for Corneal Edema does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the EO-2002 LoA Report. 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.
EO-2002 overview
EO-2002 is under development for the treatment of corneal edema and cataract. It is administered through intracameral route. The therapeutic candidate comprises of human corneal endothelial cells (HCECs) being developed based on magnetic cell delivery (MCD) nanoparticle platform.
Emmecell overview
Emmecell is a biotechnology company developing regenerative medicine using cell therapies focused on ophthalmic indications. The company is headquartered in Menlo Park, California, the US.
For a complete picture of EO-2002’s drug-specific PTSR and LoA scores, buy the report here.
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