GNC-039 is under clinical development by Systimmune and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 54% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how GNC-039’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.
GNC-039 overview
GNC-039 is under development for the treatment of relapsed and refractory high-grade glioma and solid tumor. The therapeutic candidate is a tetra specific octavalent, which is administered through intravenous route. It acts by targeting EGFRvIII, PDL1, 4-1BB and CD3.
The drug candidate was also under development for blood cancer.
Systimmune overview
Systimmune is a biopharmaceutical company that develops novel therapies for the treatment of cancer. The company’s technology platforms for the discovery and development of novel bio-therapeutics include antibody discovery platform to manufacture target-specific IgG producing B cells using novel miniaturized immuno-assays; process development platform to manufacture bio-therapeutics and multi-specific antibody engineering platforms. Its pipeline portfolio include bi-specific antibodies, antibody conjugates, and immuno-oncology products for the treatment of non-small cell lung cancer, glioblastoma, colon, neck, head, breast, nasopharyngeal, kidney and liver cancers. These antibodies act through systematic intervention to trigger the immune response on the cancer cells. Systimmune is headquartered in Redmond, Washington, the US.
For a complete picture of GNC-039’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.
