Recombinant Plasma Gelsolin Replacement for Cystic Fibrosis and Bronchiectasis is under clinical development by BioAegis Therapeutics and currently in Phase I for Bronchiectasis. According to GlobalData, Phase I drugs for Bronchiectasis have a 65% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Recombinant Plasma Gelsolin Replacement for Cystic Fibrosis and Bronchiectasis’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.
Recombinant Plasma Gelsolin Replacement for Cystic Fibrosis and Bronchiectasis overview
Recombinant plasma gelsolin (pGSN) is under development for the treatment of idiopathic bronchiectasis and lung injury in antibiotic resistant pneumonia . It is administered through intravenous route. It is a recombinant endogenous human protein and a key component of the innate immune system. The drug candidate is developed based on plasma gelsolin technology. It was also under development for the treatment of respiratory symptoms of cystic fibrosis
BioAegis Therapeutics overview
BioAegis Therapeutics that involves in developing therapeutics for infectious, inflammatory and degenerative diseases based on the platform of plasma gelsolin. The company is headquartered in North Brunswick, New Jersey, the US.
For a complete picture of Recombinant Plasma Gelsolin Replacement for Cystic Fibrosis and Bronchiectasis’s drug-specific PTSR and LoA scores, buy the report here.