TDI-01 is under clinical development by Graviton Bioscience and currently in Phase I for Cavernous Hemangioma (Cerebral Cavernous Malformation/Cerebral Cavernous Hemangioma). According to GlobalData, Phase I drugs for Cavernous Hemangioma (Cerebral Cavernous Malformation/Cerebral Cavernous Hemangioma) 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 TDI-01 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.
TDI-01 overview
TDI-01 is under development for the treatment of non-alcoholic steatohepatitis (NASH), coronavirus disease 2019 (COVID-19) pneumonia, idiopathic pulmonary fibrosis, pulmonary fibrosis, chronic graft versus host disease, pneumoconiosis and Cavernous Hemangioma (Cerebral Cavernous Malformation/Cerebral Cavernous Hemangioma) and unspecified rare CNS disorders. It acts by targeting Rho/Rho associated coiled-coil containing protein kinase 2 (ROCK2). It is administered through oral route.
Graviton Bioscience overview
Graviton Bioscience is a drug development company. The company is headquartered in New York City, New York, the US.
For a complete picture of TDI-01’s drug-specific PTSR and LoA scores, buy the report here.
Data Insights
From
The gold standard of business intelligence.
Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.