Tolasure is under clinical development by Biomendics and currently in Phase II for Epidermolysis Bullosa. According to GlobalData, Phase II drugs for Epidermolysis Bullosa have a 60% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Tolasure’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.
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.
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.