MEMANT-3310 is under clinical development by Antabio and currently in Phase I for Acinetobacter Infections. According to GlobalData, Phase I drugs for Acinetobacter Infections does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the MEMANT-3310 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.

MEMANT-3310 overview

MEMANT-3310 is under development for the treatment of complicated urinary tract infections, hospital-acquired bacterial pneumonia, ventilator-associated bacterial pneumonia, complicated intra-abdominal infections and hospital acquired infections caused by Gram negative pathogens, including carbapenem-resistant Enterobacteriaceae (CRE) and carbapenem-resistant A. baumannii (CRAB). It is a combination of meropenem and ANT-3310. It is administered through intravenous route. ANT-3310 acts by targeting serine beta-lactamases and meropenem acts by targeting penicillin binding protein (PBP).

Antabio overview

Antabio is a biopharmaceutical company. It develops novel antibacterials targeting drug-resistant pathogens. The company’s pipeline products comprise Metallo Beta-Lactamases inhibitors, Pseudomonas Biofilms inhibitors and others. It uses in vitro technologies and bacterial disease know-how for the development of next generation antibacterial drugs targeting severe and difficult-to-treat infections caused by multi-drug resistant gram-negative pathogens. Antabio’s therapies provide treatment of medical needs of the antibacterial space and to address infections caused by pathogens. It also acquires additional assets on gram-negative antibiotic resistant therapies. Antabio is headquartered in Labege, France.

For a complete picture of MEMANT-3310’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.