Enhancing the predictability of drug toxicity and efficacy

There is an unmet clinical need in drug development for in vitro models that reduce the risk of drug-induced toxicity and late-stage drug attrition.

In an upcoming webinar, which will be hosted on May 26, two expert speakers will be discussing how researchers can enhance the predictability of pre-clinical drug development.

This webinar, Enhancing the predictability of preclinical development, hosted by DDW and supported by PerkinElmer, will take place on 26 May at 4PM BST;  8AM PDT; 11 AM EDT; 5PM CEST.

Dr. Seyoum Ayehunie, Vice President, Scientific Research and Development, MatTek Corporation, will discuss the functionality and limitations of a novel in vitro 3D primary human cell-based tissue model for drug toxicity and efficacy studies.

This talk will be followed by a presentation from Dr. Hyelim Cho, Group Lead, Immunogenicity, Global DMPK Oncology and Rare Diseases, Takeda Pharmaceuticals, (pictured),  who will explain why developing a predictive pre-clinical assay is key to success in immuno-oncology drug development.

Key Learning Objectives:

  • How to evaluate models to establish robust and reliable preclinical investigation of drug candidates prior to entering clinical trials
  • How to gain an understanding of the advancements in preclinical model systems and assays
  • What to consider from the latest innovations and impact on bioanalytical assays

Who Should Attend:

  • Preclinical development scientists
  • Pharmacologists
  • Toxicologists
  • Bioanalytical assay development scientists
  • Analytical scientists

Register here


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