1 / 4

Anti-Infective Drug Discovery

Objective & Challenges: Objective was to identify an optimized anti-bacterial lead molecule with in vivo efficacy in relevant infection models an acceptable safety profile, and a patentable series. Challenge was to develop a more efficacious compound than the reference standard.

Télécharger la présentation

Anti-Infective Drug Discovery

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Case Study Anti-infective drug discovery 1

  2. Objective & Challenges: Objective was to identify an optimized anti-bacterial lead molecule with in vivo efficacy in relevant infection models an acceptable safety profile, and a patentable series. Challenge was to develop a more efficacious compound than the reference standard. Study design: • Compounds were designed and synthesized with variation. • 232 compounds were generated from 8 different series. • 3 molecules were identified from different series meeting the early lead criteria & 148 compounds were generated from 3 series. • 2 patentable leads were identified from structurally diverse series out which AU-XXX was nominated as candidate molecule. Outcome: • Improved potency (1-4x) with expanded spectrum of activity was observed. • In vitro to in vivo translation. • Favourable DMPK properties – Metabolically stable (MLM, RLM, PHLM) with good solubility and low serum protein binding. • No CYP liability. • Probe toxicity studies indicate better safety profile than the reference compound. 2

  3. Results: • AU-XXX Concentration (MIC) of 1-2 µg/mL against different phenotypes pathogens S. aureus, E. faecalis and E. faecium. • AU-XXX exhibited good in vitro antibacterial activity against respiratory S. pneumoniae, H. influenzae, and M. cattarrhalis. • AU-XXX was evaluated systemic and lung infection models and it demonstrated in vivo efficacy better than comparator reference drug. • Absorption, distribution, metabolism and excretion (ADME) of AU-XXX in mouse, rat and dog was favourable in support of preclinical safety studies and clinical development. • Toxicity studies were conducted in rats with dosage 200 mg/kg/day for 14 days. The incidence and severity observed was less compared to the reference compound. exhibited Minimum Inhibitory of Gram-positive pathogens in murine Microbiology capabilities: • Anti-infective research and development is a core research facility. • Key resources are fully dedicated to enable multiple anti-infectives research programs to be conducted to proof of concept. • Ability to reproduce and setup in-house assays rapidly. • Best/first in class medicinal chemistry expertise. • Full toxicology back-up to achieve IND optimally. 3

  4. Thank You For more information please visit https:/ /www.aurigeneservices.com/ To place an inquiry please visit https:/ /www.aurigeneservices.com/form/contact Mail us at contactapsl@aurigeneservices.com 4

More Related