Contezolid acefosamil is under clinical development by MicuRx Pharmaceuticals and currently in Phase III for Diabetic Foot Infection (DFI). According to GlobalData, Phase III drugs for Diabetic Foot Infection (DFI) have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Contezolid acefosamil’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.
Contezolid acefosamil overview
Contezolid acefosamil (MRX-4) is under development for the treatment of acute bacterial skin and skin structure infections (ABSSSI) caused by Gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE) and also for the treatment of diabetic foot infections. The drug candidate is administered through oral and intravenous route. It is a water-soluble prodrug form of MRX-I. MRX-I is an oxazolidinone antibiotic.
MicuRx Pharmaceuticals overview
MicuRx Pharmaceuticals (MicuRx) is a developer of antibiotics for drug-resistant bacterial infections. The company develops a pipeline of antimicrobial agents using its proprietary drug discovery platform to treat both gram-positive and gram-negative bacterial infections. It offers product candidates which include MRX-I, an oxazolidinone antibiotic, which is intended for the treatment of methicillin-resistant staphylococcus aureus and vancomycin-resistant enterococci infections. MicuRx also develops preclinical candidates for gram-positive and gram-negative bacterial infections. It has operations in the US and China. MicuRx is headquartered in Foster City, California, the US.
For a complete picture of Contezolid acefosamil’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.
