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.
(Ceftibuten + xeruborbactam) overview
The fixed dose combination of ceftibuten and xeruborbactam is under development for the treatment of complicated urinary tract infections including pyelonephritis. It is administered through oral route and acts by targeting penicillin binding protein (PBP) and beta-lactamase.
Qpex Biopharma overview
Qpex Biopharma is a biopharmaceutical company that discovers and develops therapies for infectious diseases. It is investigating ORAvance, an oral treatment beta-lactamase inhibitor targeting extended spectrum beta lactamase (ESBL) and carbapenem-resistant enterobacteriaceae (CRE) infections; OMNIvance drug against infections caused due to acinetobacter, pseudomonas, and enterobacteriaceae. The company is also developing QPX9003, a next gen synth polymyxin to treat multidrug-resistant (MDR) pseudomonas and acinetobacter infections. Qpex Biopharma is headquartered in San Diego, California, the US.
For a complete picture of (Ceftibuten + xeruborbactam)’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.