Vesigel is under clinical development by UroGen Pharma and currently in Pre-Registration for Non Muscle Invasive Bladder Cancer (NMIBC) (Superficial Bladder Cancer). According to GlobalData, Pre-Registration drugs for Non Muscle Invasive Bladder Cancer (NMIBC) (Superficial Bladder Cancer) have a 60% phase transition success rate (PTSR) indication benchmark for progressing into Marketed. GlobalData’s report assesses how Vesigel’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.
Vesigel overview
VesiGel is under development for the treatment of low-grade intermediate risk non muscle invasive bladder cancer (NMIBC). VesiGel is a sustained release formulation of a high dose mitomycin C. It is administered through intravesical route as a solution. It acts by targeting DNA. It is developed based on reverse thermally triggered hydrogel (RTGel) platform technology.
UroGen Pharma overview
UroGen Pharma, formerly TheraCoat, is a biotechnology company that develops and commercializes novel solutions for specialty cancers and urothelial diseases. It offers RTGel, a polymeric biocompatible and reverse thermal gelation hydrogel to improve therapeutic profiles of existing drugs and Jelmyto for pyelocalyceal solution. The company pipeline products include UGN-102, which treats non-muscle invasive urothelial cancer; UGN-301 for High-grade non-muscle-invasive bladder cancer. UroGen Pharma is headquartered in Ra Anana, Israel.
For a complete picture of Vesigel’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.
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.
