Tolasure is under clinical development by Biomendics and currently in Phase II for Epidermolysis Bullosa. According to GlobalData, Phase II drugs for Epidermolysis Bullosa does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Tolasure LoA Report. Buy the report here.
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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.
Tolasure overview
Tolasure is under development for the treatment of severe epidermolysis bullosa simplex, chronic and acute wounds, burns, skin ulcers, inflammatory disease conditions including psoriasis, dermatitis, and scleroderma, for the treatment of bacterial infections caused by highly resistant bacterial strains including methicillin-resistant Staphylococcus aureus (MRSA), Escherichia coli, Pseudomonas aeruginosa, Acinetobacter baumannii and fungal infections caused by Candida albicans. The drug candidate is a topical gel formulation containing small-molecule liquid crystals.
Biomendics overview
BioMendics, is a healing technology company using liquid crystalline biomimetics for the treatment of chronic wounds. The company is headquartered in United States.
For a complete picture of Tolasure’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.
