The old paradigm of one blockbuster drug that works for everyone has already become ancient history. As pharma evolves and recognizes the uniqueness of each individual disease, there is a growing certainty based on new methods of molecular analysis that particular drugs work better in subsets of patients who could not be previously identified or segregated. In previous clinical trials, there have been subsets of patients that either thrived on the drug and others who reaped nothing but side effects from the drug being studied. By personalizing medicine, however, and making use of information about a person’s genes, proteins, and environment, we are now better able to prevent, diagnose, and treat disease. |