Wednesday, May 24, 2017

News:: FDA approves a more 'personalized' cancer drug

Cancer treatments are becoming more personal. The Food and Drug Administration recently gave accelerated approval for Keytruda, a pre-existing drug from Merck, for use on patients diagnosed with solid tumors containing a specific biomarker. Rather than basing treatment on where the mutation originated, Keytruda will be used to treat microsatellite instability-high (MSI-H) cancers, those that are mismatch repair deficient (dMMR) and are otherwise not able to be surgically removed. These types of tumors affect how the DNA is repaired inside the cell.

Via: Regulatory Affairs Professionals Society

Source: FDA, Merck



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