Explore our active and completed clinical studies across oncology, neurology, rare diseases, and regenerative medicine. All trials adhere to rigorous global ethical and regulatory standards.
All Aevum Zenth clinical trials are conducted in strict accordance with the Declaration of Helsinki, ICH-GCP guidelines, and applicable national regulations (FDA, EMA, PMDA, NMPA). Patient safety, informed consent, and data integrity remain our highest priorities.
Independent Data Safety Monitoring Boards (DSMBs) oversee all Phase II+ trials. Raw de-identified datasets are available for qualified academic collaborators upon IRB approval.
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