ELA-026 is under clinical development by Electra Therapeutics and currently in Phase I for Hemophagocytic Lymphohistiocytosis. According to GlobalData, Phase I drugs for Hemophagocytic Lymphohistiocytosis have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ELA-026’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.
ELA-026 overview
ELA-026 is under development for the treatment of secondary hemophagocytic lymphohistiocytosis (sHLH), T cell lymphoma, T cell acute lymphoid leukaemia. It is administered by subcutaneous and intravenous route in the form of solution. It acts by targeting signal regulatory protein-alpha/beta-1/gamma.
It was under development for the treatment of other inflammatory diseases.
Electra Therapeutics overview
Electra Therapeutics is an operator of a biotechnology company that develops monoclonal antibodies designed for the treatment of immunological diseases and cancer. The company is headquartered in San Francisco, California, the US.
For a complete picture of ELA-026’s drug-specific PTSR and LoA scores, buy the report here.
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