New ADME e-book is out: In vitro toxicology
1 December 2017
Drug-induced toxicity is one of the main reasons for drug attrition. Identifying the potential safety liablities at the early stages of drug discovery projects enables designing out the risk factors and thus increases the chances to avoid failures at a later stage.
In vitro toxicology e-book provides a comprehensive overview of early safety screenings. The main focus is on hepatotoxicity, cardiotoxicity and genotoxicity assays, but the e-book covers also other forms of toxicity, like immunogenicity, steatosis, phospholipidosis and cholestasis. Furthermore, the e-book will also shed a light on to exploratory toxicity models, like 3D and stem cell derived models.
Got interested? You can download the In vitro Toxicology e-book from our website.
Check out our blog
Have you noticed that FDA has released a new draft guidance on drug-drug interaction studies? The new guideline has two complementary documents, one for in vitro and another one for in vivo studies. Read our newest blog post to discover what kind of impact the new draft guidance has on metabolism mediated DDI studies in vitro.