The future of clinical trials: more transparency and pharmacogenomics.
| Jurisdiction | United States |
| Author | Rajasimha, Harsha K. |
| Date | 01 January 2014 |
The traditional approach to Pharma clinical trials is to treat the general population as a single group. This has resulted in a large number of failures and lost opportunities in bringing new cures to market. The problem with this approach is that most candidate drugs are not effective on 100% of the population. In fact, a good number of drugs that are considered safe on a majority of the population are known to have undesirable side-effects on a small proportion of the population. Hence, there is a need for designing clinical trials that would identify patient...
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