Enamptcumab is under clinical development by Aqualung Therapeutics and currently in Phase II for Lung Injury. According to GlobalData, Phase II drugs for Lung Injury does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Enamptcumab 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.
Enamptcumab overview
Enamptcumab is under development for the prevention and treatment of acute respiratory distress syndrome, acute lung injury, ventilator-induced lung injury, radiation induced lung injury, idiopathic pulmonary fibrosis, inflammatory bowel diseases, NASH, systemic lupus vasculitis/DAH and prostate cancer, fibrosis of cardiac (post ischemic), Chorioamnionitis and pulmonary arterial hypertension. The drug candidate is administered through intravenous route. The drug candidate is humanized monoclonal antibody acts by targeting nicotinamide phosphoribosyl transferase (NAMPT).
Aqualung Therapeutics overview
Aqualung Therapeutics, is developing a novel, anti-inflammatory monoclonal antibody strategy to treat serious unchecked inflammation. The company is headquartered in United States.
For a complete picture of Enamptcumab’s drug-specific PTSR and LoA scores, buy the report here.
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