Polyrizon signed an agreement with a global preclinical contract research organization to run biocompatibility studies under ISO 10993 and GLP requirements. The studies are expected to begin in Q2 2026 and include cytotoxicity, sensitization, intracutaneous reactivity, acute systemic toxicity, and pyrogenicity assessments. CEO Tomer Izraeli said the work is intended to support regulatory submissions ahead of planned clinical trials later in 2026.
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