XPOVIOTM

Synthetic RoyaltyTM / Debt FinancingUp to $175 Million

JUNE 2021/SEPT 2019

PRODUCTXPOVIOTM

In July 2019, XPOVIOTM (selinexor) received accelerated approval from the U.S. Food and Drug Administration for the treatment of heavily pretreated adult patients with relapsed or refractory multiple myeloma. In addition to the initial indication, selinexor is being studied in several additional clinical trials in various indications and combinations.

Background

HCR completed a $75 million SYNTHETIC ROYALTYTM financing with Karyopharm following the approval of XPOVIOTM in September 2019.  That agreement contemplated a potential additional financing of up to $75 million if the company met certain key milestones, including achieving certain levels of XPOVIOTM sales and approval in different indications.  The company achieved both those milestones and the two parties were able to reach agreement on an upsized additional $100 million transaction to support further commercialization of XPOVIOTM as well as support development activities.

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