Nice research Auk as always.
Here's another piece to the puzzle. Its the Aussie TGA PAR (public assessment report) for Thromboreductin also proposed as an extended release drug. The application was made by Orphan Australia Pty Ltd as an alternative to Shire's Agrylin for ET. It was rejected by the TGA on manufacturing control grounds among others.
https://www.tga.gov.au/sites/default/files/auspar-anagrelide-hydrochloride-120507.pdf
The PDE-3 implications for the Anagrelide metabolite are also mentioned below.
By the way once the Artimist issue is sorted we will also get an rejection/approval paper a bit like this one above.
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