New analysis shows that more medicines worldwide are available to U.S. patients
A new analysis identified 220 new molecular entities (NMEs) launched in 36 countries from 2011 to 2017.
A new analysis identified 220 new molecular entities (NMEs) launched in 36 countries from 2011 to 2017.
In the past year, we have seen revolutionary new treatments become available to patients in the United States for cancer and other debilitating diseases. A new analysis puts in perspective the greater availability of new therapies for American patients compared to those living in other countries.
Using regulatory approval data from the U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA) and the Japanese Pharmaceuticals and Medical Devices Agency (PMDA), as well as product sales data from around the world, the analysis identified 220 new molecular entities (NMEs) launched in 36 countries from 2011 to 2017.
Nearly 90 percent of these newly launched medicines were available in the United States, compared to just two-thirds in the United Kingdom, half in Canada and France, and one-third in Australia. For example:
Access to life-saving treatments makes a real difference in the lives of American patients. The National Cancer Institute announced on Tuesday that cancer deaths in the United States steadily declined for all ethnic groups from 1995 to 2015. Our market-based system for prescription drugs helps American patients get more treatments than anywhere else in the world. Patients in the United States have more choices as they work with their doctors to determine the best treatment options.