![]() We are very pleased to have reached these important agreements with both the German payer association, National Association of Statutory Health Insurance Funds (GKV-SV), and the early access granted by the French Haute Autorité de Santé (HAS). Market access were secured in two of the five major European markets, namely in France on an early access basis and in Germany - two countries with more than 5,600 kidney transplants annually, of which approximately 75% are transplanted from a deceased donor. During the first quarter of 2022, we have seen additional key transplant centers becoming both clinically and commercially ready to use Idefirix ® and solid sales growth. “Hansa’s commercial launch activities and market access efforts for Idefirix ® in Europe continue to progress as planned. Søren Tulstrup, President and CEO of Hansa Biopharma, comments Number of employees at the end of the period number of shares before and after dilution The first patient is expected to be enrolled in 2022, as previously guided.įinancial summary SEKm, unless otherwise stated – unaudited Anti-GBM: On April 19, 2022, Hansa announced that the US FDA has accepted Hansa’s Investigational New Drug (IND) application to proceed with a Phase 3 study of imlifidase in 50 patients across EU and the U.S.To accelerate enrollment rate, we have implemented a number of initiatives to address the current situation and we expect these intiatives to support the completion of enrollment of GBS patients in H2 2022. The COVID-19 pandemic has significantly impacted the enrollment rate in our GBS trial at the participating hospitals. GBS: In the Guillain Barré Syndrome (GBS) Phase 2 trial, 16 patients out of a target of 30 patients have been enrolled.AMR: In the Antibody Mediated Rejection (AMR) Phase 2 trial, 28 out of a target of 30 patients have been enrolled, and completion of enrollment is expected in the first half of 2022, as previously guided.open-label, randomized, controlled trial “ConfIdeS” with the aim of completing enrollment by the end of this year, as previously guided. ConfIdeS: 16 patients have been enrolled for randomization in our pivotal U.S. The partnership with Sarepta investigating imlifidase in gene therapy and the preclinical collaboration with argenx exploring the potential for combination therapy with imlifidase moved forward according to plan.As part of the agreement, Hansa received a USD 5 million upfront payment, while AskBio has received an exclusive option to negotiate a full development and commercialization agreement. In January, Hansa and AskBio entered into an agreement to evaluate the potential use of imlifidase as a pre-treatment prior to the administration of AskBio’s investigational gene therapy in Pompe disease in a preclinical and clinical feasibility program for patients with pre-existing neutralizing antibodies (NAbs).The publication recognizes the study’s significance in autoimmune diseases as it suggests that deactivation of autoantibodies could alter the course of an autoimmune disease. Key data from a Phase 2 program of imlifidase in anti-Glomerular Basement Membrane (anti-GBM) disease patients were published in the Journal of American Society of Nephrology (JASN). ![]()
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