Zelluna ASA announced the selection of Medpace as the contract research organization (CRO) to support the first-in-human clinical trial of its lead product candidate, ZI-MA4-1 (ZIMA-101). Medpace will provide comprehensive clinical development services, including clinical operations and trial management, regulatory support, data management and analysis, and pharmacovigilance. This partnership follows the submission of a Clinical Trial Application $(CTA)$ to the MHRA and supports Zelluna's transition to a clinical-stage company as it prepares to initiate the study pending regulatory approval.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Zelluna ASA published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW1001164101-en) on February 11, 2026, and is solely responsible for the information contained therein.
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