PBF-680 is under clinical development by Palo BioFarma and currently in Phase II for Chronic Obstructive Pulmonary Disease (COPD). According to GlobalData, Phase II drugs for Chronic Obstructive Pulmonary Disease (COPD) have a 25% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how PBF-680’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.
PBF-680 overview
PBF-680 is under development for the treatment of asthma and chronic obstructive pulmonary disease (COPD). The drug candidate is formulated as capsule and administered orally. It acts by targeting adenosine A receptor (ADORA1). It is chemically a non-xanthine with non BBB (Blood Brain Barrier) permeability.
Palo BioFarma overview
Palo BioFarma is a Spanish biotechnology company. The scientists with experience in drug discovery in several pharmaceutical companies and mission of the Palobiofarma is to discover new drugs based on the modulation of adenosine receptors. The company is headquartered Mataró, Barcelona, Spain.
For a complete picture of PBF-680’s drug-specific PTSR and LoA scores, buy the report here.
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