Hansa Biopharma announces encouraging high-level results for first-in-human trial of HNSA-5487
- Results showed HNSA-5487 to be safe and well tolerated
- Fast and complete depletion of IgG antibodies observed at increasing doses
- Pharmacokinetics (PK) in line with expectations
- Pharmacodynamics (PD) showed fast and complete cleavage of IgG to F(ab')2- and Fc-fragments with increasing doses
- HNSA-5487 is the lead candidate in the NiceR program aiming to develop next-generation enzymes with lower immunogenicity
- Enzyme with lower immunogenicity could enable repeat dosing and innovative treatment approaches in various indications
- None.
HNSA-5487 is a next-generation IgG-cleaving enzyme and the lead candidate in the NiceR development program
NICE-01 is a double blind, randomized, placebo-controlled trial evaluating safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of single ascending doses of HNSA-5487 administered as a single intravenous (IV) infusion. The trial included a total of 36 healthy male and female adult participants.
HNSA-5487 is the company's lead candidate in the Novel Immunoglobulin Cleaving Enzymes for Repeat Dosing (NiceR) program. The NiceR program aims to develop next-generation enzymes with lower immunogenicity that would potentially allow for repeat dosing in a range of indications including IgG-driven autoimmune diseases where patients experience flares, transplantation where repeat dosing would be beneficial, gene therapy and oncology.
Søren Tulstrup, President and CEO, Hansa Biopharma said, "This is encouraging data as we continue to explore the potential for HNSA-5487 and better understand how this powerful, new enzyme could benefit patients and clinicians. An enzyme with lower immunogenicity would potentially enable repeat dosing, allowing a prolonged effect by flexibly extending the IgG-free window depending on the number of repeated infusions. This could enable innovative treatment approaches in a broad range of indications, and benefit patients with diseases where a prolonged IgG-free window is needed".
Analysis of additional exploratory endpoints on IgG recovery and immunogenicity is now being conducted, with follow up on all subjects for 12 months. This analysis will serve as key input in determining the further clinical development program, including selection of indications.
For further information, please contact:
Klaus Sindahl, VP Head of Investor Relations
M: +46 (0) 709–298 269
E: klaus.sindahl@hansabiopharma.com
Stephanie Kenney, VP Global Corporate Affairs
M: +1 (484) 319 2802
E: stephanie.kenney@hansabiopharma.com
The following files are available for download:
20231009-HNSA-5487 FIH -FINAL_en |
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SOURCE Hansa Biopharma AB
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