Answers are grounded in this paper and cite their sources.
The "Right-to-Try" experimental drugs act passed by Donald Trump in 2018 provides an opportunity of early access to experimental drugs for the treatment of life-threatening diseases and a potential boon to many young and under-capitalized biotechnology or pharmaceutical companies. The pros and cons of experimental drugs, including a number of "cutting edge" scientific, clinical, and a number of synergistic approaches such as artificial intelligence, machine learning, big data, data refineries, electronic health records, data driven clinical decisions and risk mitigation are reviewed.
No takes yet. Share an insight, caveat, or question.
Vijay Mahant (2020) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: