Hansa hosts call with distinguished transplant surgeons: Insights on clinical practice and imlifidase Phase 3 Results

Rhea-AI Summary

Hansa (Nasdaq: HNSA) will host a virtual event on Wednesday 12 November 2025 at 9:00 AM EST / 15:00 CET featuring transplant surgeons Professor Robert Montgomery and Professor Matthew Cooper.

The session includes an introduction by CEO Renée Aguiar-Lucander, presentation of topline results from the US Phase 3 ConfIdeS trial by CMO Richard Philipson, a moderated discussion on clinical practice and the medical need for highly sensitized kidney transplant patients, and a live Q&A.

The event aims to provide clinician perspectives on the clinical relevance of the ConfIdeS topline results and potential implications for standard of care in the US transplant community.

LUND, Sweden, Oct. 29, 2025 /PRNewswire/ -- Hansa Biopharma AB, "Hansa" (Nasdaq Stockholm: HNSA) today announced that it will host a virtual event featuring two distinguished transplant surgeons; Professor Robert Montgomery from NYU Langone Transplant Institute and Professor Matthew Cooper from the Medical College of Wisconsin, to provide deeper insights into the medical journey of highly sensitized patients awaiting a kidney transplant and share perspectives on the clinical relevance of the topline results from the US Phase 3 ConfIdeS study.  The event will take place on Wednesday 12 November, 2025, at  9:00 AM EST / 15:00 PM CET. Click here to join.

After an introduction by Renée Aguiar-Lucander, CEO, Hansa Biopharma, there will be a presentation of the topline results from the US Phase 3 ConfIdeS trial by Richard Philipson, CMO. Philipson will then moderate a discussion reviewing current challenges of highly sensitized patients, the medical need and existing clinical practice for this patient group as well as the clinical relevance of the ConfIdes topline results, and the potential to impact current standard of care within the US transplant community with Dr. Robert Montgomery, MD, PhD, NYU Langone Transplant Institute, and Dr. Matthew Cooper, MD, Medical College of Wisconsin, followed by a Q&A session.

About Robert Montgomery, MD, PhD

Dr. Robert Montgomery is Chair of the Department of Surgery and Director of the NYU Langone Transplant Institute. As a pioneer and international expert in desensitization, he has taken part in numerous research studies, publications, and has received many awards for his work. Throughout his career, Dr. Montgomery has led innovation in transplantation, credited with developing and performing the first 'domino paired donation' and now leading efforts in xenotransplantation. He is also a heart transplant recipient himself. Dr Montgomery acted as Lead Principal Investigator for the ConfIdeS trial.

About Matthew Cooper, MD

Dr. Matthew Cooper is Chief of Transplantation, Director of Solid Organ Transplant, and the Mark B. Adams Distinguished Professor of Surgery at the Medical College of Wisconsin. He currently serves as a board member for the American Society of Transplantation (AST) and the National Kidney Foundation (NKF) and is the Surgical Director for the National Kidney Registry (NKR). Dr. Cooper is a former President of the United Network for Organ Sharing (UNOS) and the Organ Procurement and Transplantation Network (OPTN). He has authored over 260 peer-reviewed manuscripts, 300 abstracts, and 12 book chapters and has received numerous awards in the field of kidney transplantation. Dr Cooper acted as Principal Investigator for the ConfIdeS trial.

Link to Virtual Event: https://lifescievents.com/event/gl39mp2j/

Contacts for more information:

Evan Ballantyne, Chief Financial Officer
IR@hansabiopharma.com

Kerstin Falck, VP Global Corporate Affairs
media@hansabiopharma.com

Notes to editors

About highly sensitized patients

Highly sensitized patients have pre-formed antibodies called donor specific antibodies (DSAs) with a broad reactivity against human leukocyte antigens (HLAs), which can cause tissue damage and potentially transplant rejection.¹ The presence of DSAs means that highly sensitized patients tend to have limited or no access to transplant, as finding a compatible donor organ can be particularly challenging.^2,3 The complexity of their immunological profile means that highly sensitized patients spend longer time than average on transplant waiting lists, with evidence showing that this longer time waiting for a suitable donor relates to an increased mortality risk.^4,5 Across the U.S. and Europe, highly sensitized patients comprise around 10-15% of the total of patients on transplant waiting lists.^6,7

About IDEFIRIX^® (imlifidase)

Imlifidase is an antibody-cleaving enzyme originating from Streptococcus pyogenes that specifically targets and cleaves immunoglobulin G (IgG) antibodies and inhibits IgG-mediated immune response.⁸ It has a rapid onset of action, cleaving IgG-antibodies and inhibiting their activity within hours after administration.

Imlifidase has conditional marketing approval in Europe and is marketed under the trade name IDEFIRIX for the desensitization treatment of highly sensitized adult kidney transplant patients with a positive crossmatch against an available deceased donor. The use of IDEFIRIX should be reserved for patients who are unlikely to be transplanted under the available kidney allocation system, including prioritization programs for highly sensitized patients.⁸ IDEFIRIX was reviewed as part of the European Medicines Agency's (EMA) PRIority Medicines (PRIME) program, which supports medicines that may offer a major therapeutic advantage over existing treatments or benefit patients without treatment options.⁸

Imlifidase is a promising new strategy for desensitization of transplant patients with donor-specific anti-HLA (Human Leukocyte Antigens) antibodies (DSAs).⁹ Highly sensitized patients have high levels of these preformed antibodies that can bind to the donor organ and damage the transplant.¹ Once they are inactivated with imlifidase, there is a window of opportunity for the transplant to take place. By the time the body starts to synthesize new IgG, the patient will be receiving post-transplant immunosuppressive therapy to reduce the risk of organ rejection.

The efficacy and safety of imlifidase as a pre-transplant treatment to reduce donor-specific IgG was studied in four phase 2 open-label, single-arm, six-month clinical trials.^7,9-11 Hansa is collecting further clinical evidence and will submit additional efficacy and safety data based on one observational follow-up study and one post-approval efficacy study.

Full product information can be accessed via the initial Summary of Product Characteristics found here.

About kidney failure

Kidney disease can progress to kidney failure or End-Stage Renal Disease (ESRD), identified when a patient's kidney function is less than 15%.¹² ESRD poses a significant health burden, affecting nearly 2.5 million patients worldwide.¹² A kidney transplant is the treatment of choice for suitable patients with ESRD because it offers improved survival and quality of life benefits, and is cost savings compared to long-term dialysis. There are approximately 170,000 kidney patients in the U.S. and Europe waiting for a new kidney.¹³

About Hansa Biopharma

Hansa Biopharma AB is a pioneering commercial-stage biopharmaceutical company on a mission to develop and commercialize innovative, lifesaving and life-altering treatments for patients with rare immunological conditions. The company has a rich and expanding research and development program based on its proprietary IgG-cleaving enzyme technology platform, to address serious unmet medical needs in autoimmune diseases, gene therapy and transplantation. The company's portfolio includes imlifidase, a first-in-class immunoglobulin G (IgG) antibody-cleaving enzyme therapy, which has been shown to enable kidney transplantation in highly sensitized patients and HNSA-5487, a next-generation IgG cleaving molecule with redosing potential. Hansa Biopharma is based in Lund, Sweden, and has operations in Europe and the U.S. The company is listed on Nasdaq Stockholm under the ticker HNSA. Find out more at www.hansabiopharma.com and follow us on LinkedIn.

©2025 Hansa Biopharma AB. Hansa Biopharma, the beacon logo, IDEFIRIX, and IDEFIRIX flower logo are trademarks of Hansa Biopharma AB, Lund, Sweden. All rights reserved.

References

1_Eurostam Report (A Europe-wide strategy to enhance transplantation of highly sensitized patients on the basis of acceptable HLA mismatches.) Available at https://cordis.europa.eu/project/id/305385/reporting.

2_Redfield RR, et al. The mode of sensitization and its influence on allograft outcomes in highly sensitized kidney transplant recipients. Nephrol Dial Transplant. 2016 Oct;31(10):1746-53. doi: 10.1093/ndt/gfw099.

3_Lonze BE, et al. IdeS (Imlifidase): A Novel Agent That Cleaves Human IgG and Permits Successful Kidney Transplantation Across High-strength Donor-specific Antibody. Ann Surg. 2018 Sep;268(3):488-496. doi: 10.1097/

4_Alelign T, Ahmed MM, Bobosha K, Tadesse Y, Howe R, Petros B. Kidney Transplantation: The Challenge of Human Leukocyte Antigen and Its Therapeutic Strategies. J Immunol Res. 2018 Mar 5;2018:5986740. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859822/

5_Heidt S, et al. Highly Sensitized Patients are Well Serves by Recieving a Compatible Organ Offer Based on Acceptable Mismatches. Front Immunol. 2021;12:687254. Available at: https://pubmed.ncbi.nlm.nih.gov/34248971/

6_Organ Procurement and Transplantation Network (OPTN) and Scientific Registry of Transplant Recipients (SRTR). OPTN/SRTR 2022 Annual Data Report. U.S. Department of Health and Human Services, Health Resources and Services Administration; 2024. Accessed [June 2024].

7_Jordan SC, et al. Imlifidase Desensitization in Crossmatch-positive, Highly Sensitized Kidney Transplant Recipients: Results of an International Phase 2 Trial (Highdes). Transplantation. 2021 Aug 1;105(8):1808-1817. doi: 10.1097/TP.0000000000003496.

8_European Medicines Agency. Idefirix^® summary of product characteristics. Available at: https://www.ema.europa.eu/en/documents/product-information/idefirix-epar-product-information_en.pdf.

9_Jordan SC, et al. IgG Endopeptidase in Highly Sensitized Patients Undergoing Transplantation. N Engl J Med  2017;377:442-453. DOI: 10.1056/NEJMoa16125

10_Winstedt L, et al. Complete Removal of Extracellular IgG Antibodies in a Randomized Dose-Escalation Phase I Study with the Bacterial Enzyme IdeS--A Novel Therapeutic Opportunity. PLoS One. 2015 Jul 15;10(7):e0132011. doi: 10.1371/journal.pone.0132011. PMID: 26177518; PMCID: PMC4503742.

11_Lorant T, et al. Safety, immunogenicity, pharmacokinetics, and efficacy of degradation of anti-HLA antibodies by IdeS (imlifidase) in chronic kidney disease patients. Am J Transplant. 2018 Nov;18(11):2752-2762. doi: 10.1111/ajt.14733.

12_NIH (2018). What is kidney failure? Available at: https://www.niddk.nih.gov/health-information/kidney-disease/kidney-failure/what-is-kidney-failure.

13_ Newsletter Transplant 2022. International figures on donation and transplantation. Available at: Newsletter Transplant - latest edition I Freepub (edgm.eu) Accessed: May 2024

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SOURCE Hansa Biopharma AB

FAQ

When is Hansa's virtual event on the ConfIdeS Phase 3 topline results (HNSA)?

The event is scheduled for Wednesday 12 November 2025 at 9:00 AM EST / 15:00 CET.

Who will present and speak at Hansa's HNSA event about highly sensitized kidney transplant patients?

Speakers include CEO Renée Aguiar-Lucander, CMO Richard Philipson, Professor Robert Montgomery, and Professor Matthew Cooper.

What will be presented about the ConfIdeS US Phase 3 trial during the HNSA event?

CMO Richard Philipson will present the topline results from the US Phase 3 ConfIdeS trial followed by a clinician discussion and Q&A.

How can investors or clinicians join Hansa's HNSA virtual presentation on November 12, 2025?

The event is virtual; interested parties can join via the company's provided registration/link to the webcast.

What topics regarding highly sensitized patients will Hansa cover in the HNSA webcast?

The discussion will cover current challenges, medical need, existing clinical practice, and the clinical relevance of the ConfIdeS topline results for US transplant care.

Will there be an interactive segment during Hansa's HNSA ConfIdeS presentation?

Yes; the program includes a moderated discussion followed by a live Q&A session with the speakers.