AAV-hTERT is under clinical development by Libella Gene Therapeutics and currently in Phase I for Critical Limb Ischemia. According to GlobalData, Phase I drugs for Critical Limb Ischemia 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 AAV-hTERT 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.
AAV-hTERT overview
Gene Therapy is under development for the treatment of ageing and critical limb ischemia. The therapeutic candidate is administered by intravenous, intravascular and intrathecal routes. It is developed based on Adeno-associated virus (AAV) reverse (hTERT) transcriptase enzyme technology. The therapeutic candidate acts by delivering human telomerase reverse transcriptase (hTERT) gene.
It was also under development for the treatment of Alzheimer's disease.
For a complete picture of AAV-hTERT’s drug-specific PTSR and LoA scores, buy the report here.
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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.
