AGT103-T is under clinical development by Addimmune and currently in Phase I for Human Immunodeficiency Virus (HIV) Infections (AIDS). According to GlobalData, Phase I drugs for Human Immunodeficiency Virus (HIV) Infections (AIDS) have a 70% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how AGT103-T’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.
AGT103-T overview
AGT103-T is under development for the treatment of HIV. It is administered by parenteral route. The drug candidate is a genetically modified autologous T cell therapy transduced with lentiviral vector. It acts by targeting CCR5, reverse transcriptase and TAR.
Addimmune overview
Addimmune is a biotechnology research company which focuses on gene therapy approach to cure HIV and improve lives of individual. The company is headquartered in Rockville, Maryland, the US.
For a complete picture of AGT103-T’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 clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
