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      Plenary Presentation at the 2019 American Transplant Congress Demonstrates Significant Reduction in Time on the Waitlist for Patients Treated with Imlifidase Compared to Matched Controls

      Session Wins ATC's People's Choice Award


      News provided by

      Hansa Biopharma AB

      Jun 07, 2019, 02:15 ET

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      LUND, Sweden, June 7, 2019 /PRNewswire/ -- Hansa Biopharma AB ("Hansa") (NASDAQ Stockholm: HNSA), the leader in immunomodulatory enzyme technology for rare IgG-mediated diseases, announced today that IDEFIRIXTM (imlifidase), the company's novel IgG-degrading enzyme, was highlighted in three presentations at the 2019 American Transplant Congress (ATC), which was held from June 1 – 5, 2019 in Boston, Massachusetts, USA.

      In a plenary presentation on June 5, 2019, Dr. Edmund Huang, MD, Associate Professor and Transplant Nephrologist at the Kidney and Pancreas Transplant Center at Cedars-Sinai Medical Center in Los Angeles, presented "Three-year Outcomes of Highly-sensitized Kidney Transplant Recipients Desensitized with IgG Endopeptidase." The plenary abstract, by Dr. Huang and Stanley Jordan M.D., Director Kidney Transplantation and Transplant Immunology at the Cedars-Sinai Medical Center in Los Angeles, won the ATC's People's Choice Award, as voted by the ATC attendees to be the most impactful to the transplant community.

      In his presentation, Dr. Huang reported a statistically significant reduction in time on the waitlist for transplantation among imlifidase treated patients compared to similarly sensitized matched controls. The matched control analysis showed statistically significant shorter time to transplant in both the current and previous U.S. Kidney Allocation System (KAS).

      "Our matched control analysis showed statistically significant shorter time to transplant in the pre and post- KAS era. We are therefore convinced that Imlifidase complements the new KAS system and will facilitate reduced time to kidney transplantation in highly sensitized patients." commented Dr. Huang

      "We have previously demonstrated that treatment with imlifidase enables life-saving kidney transplantation that would otherwise not be possible. This matched control analysis further illustrates shorter time to transplant for these highly sensitized patients" commented Dr. Jordan.

      The presentation also reported follow up data from the U.S. investigator-initiated Phase 2 study of imlifidase for kidney transplantation in highly sensitized patients. Results show excellent graft survival out to three years with graft survival in line with deceased donor transplantation of non-sensitized patients. One death, unrelated to imlifidase treatment and the kidney transplant, occurred 10 months after transplant. There were sporadic cases of late rebound DSA, but most remained DSA-free up to 36 months post-transplant.

      In an oral presentation on June 2, 2019, Robert A. Montgomery, M.D., Director, NYU Langone Transplant Institute, New York City, presented "Safety and Efficacy of Imlifidase in Highly-Sensitized Kidney Transplant Patients: Results from a Phase 2 Study."

      "The safety and efficacy data on imlifidase provide hope to highly sensitized patients, who today are very difficult or impossible to transplant, and face an extremely poor prognosis. Six months follow up results continue to show that imlifidase has enabled all patients to undergo transplantation resulting in good kidney function and graft survival," Robert A. Montgomery, M.D., Director, NYU Langone Transplant Institute, New York City.

      In a poster session on June 2, 2019, Dr. Matthew J. Everly, Director of the Terasaki Research Institute in Los Angeles, presented "A Prognostic Drug Development Tool to Assess the Transplantability at the Time of Listing for Kidney Transplant Candidates."

      In his poster session Dr. Everly reported on the results of simulations done in highly sensitized patients, which demonstrated that transplant rates could be increased by 25% if there were a therapy to address the HLA antibody barrier.

      References

      1. https://optn.transplant.hrsa.gov

      The information was submitted for publication, through the agency of the contact person set out below at 08:00am CET on June 7, 2019.

      For further information, please contact:

      Company:

      Klaus Sindahl
      Head of Investor Relations
      Hansa Biopharma
      Mobile: +46 (0) 709-298 269
      E-mail: [email protected] 

      Rolf Gulliksen
      Head of Corporate Communications
      Hansa Biopharma
      Mobile: +46 (0) 733-328 634
      E-mail: [email protected]

      Swedish Investor and Media Relations:

      Cord Communications

      Mikael Widell
      +46 70-311 99 60

      U.S. Investor and Media Relations:

      Argot Partners
      Stephanie Marks / David Rosen (media)
      +1-212-600-1902

      This information was brought to you by Cision http://news.cision.com

      https://news.cision.com/hansa-biopharma-ab/r/plenary-presentation-at-the-2019-american-transplant-congress-demonstrates-significant-reduction-in-,c2835590

      The following files are available for download:

      https://mb.cision.com/Main/1219/2835590/1058815.pdf

      Plenary Presentation at the 2019 American Transplant Congress Demonstrates Significant Reduction in Time on the Waitlist for Patients Treated with Imlifidase Compared to Matched Controls; Session Wins ATC’s People’s Choice Award

      SOURCE Hansa Biopharma AB

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