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April 3, 2014
13:49 EDTRTRXRetrophin notifies Chenodal wholesaler of price increase
Retrophin disclosed in a regulatory filing that the company provided notice to the wholesaler of its Chenodal product that, effective immediately, Retrophin had increased the price of a package of 100 250mg tablets of Chenodal from $9,460 to $47,300.
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November 17, 2015
09:12 EDTRTRXRetrophin management to meet with Leerink
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November 16, 2015
08:09 EDTRTRXRetrophin receives EU ODD for sparsentan
Retrophin announced that the European Commission, or EC, has granted sparsentan orphan drug designation for the treatment of focal segmental glomerulosclerosis, or FSGS. Retrophin previously announced in January 2015 that sparsentan received orphan drug designation from the FDA for the treatment of FSGS. Sparsentan is the company's investigational therapeutic agent which acts as both a potent angiotensin receptor blocker, as well as a selective endothelin receptor antagonist, and is currently being evaluated in the Phase 2 DUET trial in FSGS patients. FSGS is a widely recognized cause of end-stage renal disease and there are no approved pharmacologic treatments currently available in the United States or Europe.

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