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FDA no longer needs to require animal tests before human drug trials, We are an international end user assessed ethically compliant and technically competent HBS provider through Science Exchange platform
Catalogue Name :
ImmunoTOX
Solution Type:
DART

In Stock

ImmunoTOX A non-animal new approach methodology to test predict human immunotoxicity concerns

Cell type used as testing platform
TRANS-HSC: Characterized Configured Human Hematopoietic type of adult primary and progenitors
Insilico platform used to publish the report
ImmunoTOX software (trained on Convolutional Neural Network)
Assay endpoints:
ImmunoTOX
Immunotoxicity is referred as one of the adverse effects of immune system both local and systemic that result from exposure to compounds/drugs including vaccines. It is evidently demonstrated from clinical data that there is significant morbidity occurred due to immunotoxicity. According to immunotoxicity testing guidance from FDA the five major categories to study immunotoxicity are:

  • Hypersensitivity
  • Inflammation
  • Immunosuppression
  • Immunostimulation and auto immunity

Reference:
Avila AM, Bebenek I, Bonzo JA, Bourcier T, Davis Bruno KL, Carlson DB, Dubinion J, Elayan I, Harrouk W, Lee SL, Mendrick DL, Merrill JC, Peretz J, Place E, Saulnier M, Wange RL, Yao J, Zhao D, Brown PC. An FDA/CDER perspective on nonclinical testing strategies: Classical toxicology approaches and new approach methodologies (NAMs). Regul Toxicol Pharmacol. 2020 Jul;114:104662. doi: 10.1016/j.yrtph.2020.104662. Epub 2020 Apr 20. PMID: 32325112.

Available Resources

Catalogue Name :
ImmunoTOX
Solution Type:
DART

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