Latanoprost SR is under clinical development by Peregrine Ophthalmic and currently in Phase I for Unspecified Ophthalmological Disorders. According to GlobalData, Phase I drugs for Unspecified Ophthalmological Disorders 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 Latanoprost SR 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.
Latanoprost SR overview
Latanoprost sustained release formulation is under development for the treatment of lower eyelid steatoblepharon. It is administered through parenteral and subconjunctival route. The drug candidate is liposomal formulation of latanoprost. It acts by targeting prostaglandin F2-alpha receptor. The drug candidate is based on liposomal technology.
It was under development for primary open angle glaucoma and ocular hypertension.
For a complete picture of Latanoprost SR’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.
