Santhera Reports Strong Top-line Growth for 2018 and the Successful Expansion of its Rare Disease Pipeline

In This Article:

Pratteln, Switzerland, April 29, 2019 - Santhera Pharmaceuticals (SANN.SW) announces the Group`s audited financial results for 2018. The Company reports a 38% increase in net revenues year-on-year to CHF 31.7 million (2017: CHF 22.9 million) from continued growth in sales of its lead product Raxone® for the treatment of Leber`s hereditary optic neuropathy (LHON). The operating result of CHF -51.4 million predominantly reflects investments in several ongoing clinical development programs and preparations for regulatory submissions as well as commercial activities. The net result amounted to CHF -54.2 million (2017: CHF -51.5 million), in line with the Company`s guidance. Santhera successfully achieved a key objective of broadening its pipeline with clinical stage products for rare diseases with the in-licensing of POL6014 and the option to sub-license vamorolone. In the first quarter of 2019, the Company raised new liquid funds of up to CHF 22.1 million and grew sales of Raxone for LHON by 19% year-on-year, reaching CHF 9.2 million (Q1-2018: CHF 7.7 million).

"I am pleased with the progress Santhera has made during the past year. We have achieved excellent sales performance and robust revenue growth with Raxone for the treatment of LHON in 2018 and the continued expansion of our rare disease pipeline with clinical-stage drug candidates," said Thomas Meier, PhD, CEO of Santhera. "We have delivered on a strategic objective to broaden our development pipeline by acquiring rights to two highly promising drug candidates in areas with high unmet medical need, proving our ability to in-license high-quality, clinical-stage rare disease assets."

"In addition, we have focused our work on substantially strengthening our data package for idebenone in Duchenne muscular dystrophy (DMD) demonstrating clinically relevant patient benefits and sustained, long-term therapeutic efficacy. These new clinical data which collectively supports the potential for idebenone to modify the course of respiratory function decline in DMD and thereby delay the time to clinically relevant milestones will be included in our application for Conditional Marketing Authorization (CMA) in Europe. Our strategic priorities for 2019 are the submission of the CMA for Puldysa® (idebenone) to treat DMD in Europe, advancing our clinical stage pipeline, in particular vamorolone and POL6014, and securing the necessary financial resources to achieve these objectives."

Strong double-digit sales growth from Raxone® for LHON
In 2018, net revenues from product sales of Raxone for LHON reached CHF 31.7 million which corresponds to a high double-digit growth of 38% year-on-year (2017: CHF 22.9 million). Growth was primarily driven by higher market penetration and additional reimbursement schemes coming into effect. The roll-out of Raxone in the approved indication is progressing as planned with reimbursement and launches in additional countries expected in 2019.