DRI Healthcare Trust Announces Acquisition of an Additional Royalty Interest in the Worldwide Sales of Xenpozyme? (olipudase alfa) for the Treatment of Acid Sphingomyelinase Deficiency

In This Article:

– Transaction pushes total committed capital to over US$1 billion since IPO –

– Second Xenpozyme royalty increases exposure to rare diseases –

– Long-term asset further increases portfolio duration –

TORONTO, July 2, 2024 /CNW/ - DRI Healthcare Trust (TSX: DHT.UN) (TSX: DHT.U) (the "Trust"), a global leader in providing financing to advance innovation in the life sciences industry, has acquired a second royalty interest in the worldwide net sales of Xenpozyme (olipudase alfa) from HLS Therapeutics Inc. ("HLS") for an aggregate purchase price of up to US$45.75 million, comprised of a US$13.25 million upfront payment and up to US$32.5 million in performance-based outbound milestone payments.

DRI Healthcare Trust (TSX: DHT.UN/DHT.U) Logo (CNW Group/DRI Healthcare Trust)
DRI Healthcare Trust (TSX: DHT.UN/DHT.U) Logo (CNW Group/DRI Healthcare Trust)

Xenpozyme is the only product developed and approved for the treatment of non-central nervous system manifestations of acid sphingomyelinase deficiency ("ASMD"), also known as Niemann-Pick disease, in pediatric and adult patients. Xenpozyme was approved in Japan in March 2022, by the European Commission in June 2022, and by the U.S. Food and Drug Administration in August 2022. There are no other products currently known to be in late-stage development for the treatment of ASMD. Xenpozyme is marketed worldwide by Sanofi S.A. ("Sanofi").

"Xenpozyme is an important treatment that materially increases the quality of life of patients suffering from ASMD," said Behzad Khosrowshahi, the Trust's Chief Executive Officer. "The drug has performed well since our initial investment in October 2022, and we are pleased to increase our exposure to this rare disease therapy. Sanofi is the market leader in commercialization of enzyme replacement therapies ("ERT") and we believe they can facilitate access to the drug for the hundreds of ASMD patients around the globe. This long-tailed asset helps increase our portfolio duration, providing value for unitholders over the long term."

Speaking on behalf of the investment manager, Chief Investment Officer Navin Jacob commented, "ASMD is an extremely rare progressive genetic disease with significant morbidity and mortality, especially among infants and children. Signs and symptoms of ASMD may include enlarged spleen or liver, difficulty breathing, lung infections, and unusual bruising or bleeding, among others. Xenpozyme aligns with our investment criteria of treating serious disease areas and is a drug that benefits doctors, payors and most importantly, patients."

The transaction entitles the Trust to an approximately 1% royalty on worldwide sales of Xenpozyme. The Trust will receive all royalties up to US$6.3 million in royalty receipts per calendar year, with a 50% step down for all royalty receipts above this amount. Royalties will be paid bi-annually on a two-quarter lag from the half year period when sales occur. We estimate that the Trust will receive its first royalty from this entitlement in Q2 2025 based on third and fourth quarter 2024 sales.