Delay and restricted access of new molecules in Turkey compared to the United States and European Union

J Mark Access Health Policy. 2013 Nov 15:1. doi: 10.3402/jmahp.v1i0.22799. eCollection 2013.

Abstract

Objective: This study compares the performances of new-molecule (NM) launches in Turkey with those in the European Union and United States for the years 2007-2013.

Methods: The Thomson Reuters Newport Horizon for Innovators Database is used to identify NMs with a launch date after January 1, 2007, worldwide and marketing authorization approval after January 1, 2007, in the European Union. The launch dates for the European Union, the United States, and Turkey were retrieved from the same database. Data for Turkey were confirmed via IMS and RxMedia.

Results: Out of 183 records identified that are launched in the European Union, the United States, or both, 44 of the NMs are launched in Turkey (24%).

Conclusion: The results of this study show that 24% of the NMs that are launched in either the European Union or United States were able to be launched in Turkey with a mean delay of 821 days (2.25 years).

Keywords: Turkish pharmaceutical market; access to medicine; launch; new molecules.