Ceftriaxone is under clinical development by scPharmaceuticals and currently in Phase III for Gram-Positive Bacterial Infections. According to GlobalData, Phase III drugs for Gram-Positive Bacterial Infections have a 43% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Ceftriaxone’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
Ceftriaxone overview
Ceftriaxone is under development for the treatment of infections caused by gram-positive and gram-negative bacteria. The drug candidate is administered by the subcutaneous route. Ceftriaxone is a beta-lactam compound in which the beta-lactam ring is fused to a 6-membered dihydrothiazine ring. It is delivered using micropump. It acts by targeting penicillin-binding protein (PBP).
ScPharmaceuticals overview
scPharmaceuticals is a clinical-stage pharmaceutical company. The company’s pipeline products include subcutaneous formulations of furosemide, ceftriaxone and carbapenem. Its product ceftriaxone is an antibiotic used intravenously for the treatment of infections caused by gram-positive and gram-negative organisms. The company’s carbapenems are antibiotics used intravenously for the treatment of infections caused by gram-negative organisms. It also provides clinical trial services. The company operates in the US. scPharmaceuticals is headquartered in Burlington, Massachusetts, the US.
For a complete picture of Ceftriaxone’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
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.
