Software for predicting liver injury from biologics drug candidates using data from a human liver microphysiology system - the goal of this project is to develop novel technology for predicting…

Ended Project Grant Awarded Last action

Award ID
R43TR003535
Recipient
Awarding agency
Obligated
-$3

Award facts

Completion date
Place of performance
California, USA

Award details come from USAspending.gov.

Description

Software for predicting liver injury from biologics drug candidates using data from a human liver microphysiology system - the goal of this project is to develop novel technology for predicting biologics-induced liver injury such as caused by anti-inflammatory biologics such as anti-IL6 receptor antibody (e.g., tocilizumab), and by growth factors such as neuregulin-1SS isoform, glial growth factor 2 (GGF2), as well as by other biologics (e.g., checkpoint inhibitors). Biologics now account for more than half of the drugs in development, and have the potential to address many acute diseases, chronic diseases, and other unmet medical needs. Biologics-induced liver injury can manifest as focal hepatocyte necrosis, steatosis, and fibrosis. In some cases, liver transplantation is required for patients with biologics-induced liver injury. A significant problem is that while there is increased development and use of biologics, there lacks tools available for the assessment of biologics for the ability to cause biologics-induced liver injury. For example, because biologics are typically designed specifically for human targets, standard preclinical models used for small molecule drug development are inadequate for assessing the efficacy or safety of biologics. In this project, we will develop novel technology that will serve as a prototype for use in testing biologics (preclinical, clinical, or after-market) for potential to cause biologics-induced liver injury. In developing this new technology, we will also further develop the state-of-the-art human liver MPS (vlamps) to assess the liver effects of biologics from human liver cells in the liver acinus with the aim of using vlamps as the eventual key source of input data for biologxsym simulations. Additionally, we will perform validation of this new technology. Once validated, this system will serve as a prototype that can then be expanded for commercialization for use by our existing base of pharmaceutical company customers, regulatory agencies, and academic institutions for teaching and academic research use.

Transactions

Action Obligated Date
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Quick answers

Who received award R43TR003535?

R43TR003535 was awarded to Simulations Plus Inc. by National Center for Advancing Translational Sciences (National Institutes of Health) on November 13, 2021.

How much is award R43TR003535 worth?

Obligations on R43TR003535 net to -$3: more has been deobligated than obligated.

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