Fennec Pharmaceuticals reports real-world data supporting PEDMARK use after cisplatin in adult head and neck cancer patients

Reuters
02/20
Fennec Pharmaceuticals reports real-world data supporting PEDMARK use after cisplatin in adult head and neck cancer patients

Fennec Pharmaceuticals Inc. announced new real-world data on PEDMARK (sodium thiosulfate injection) use in adults with head and neck cancers from a multi-institutional retrospective review of 15 patients receiving cisplatin. The analysis evaluated feasibility of administering PEDMARK at least six hours after cisplatin, operational metrics (including home vs. clinic infusion), infusion-related events, and completion of audiology assessments; the company reported no disruption to curative-intent cisplatin delivery and no grade 3 or 4 toxicities. The results were presented as a digital poster at the 2026 Multidisciplinary Head and Neck Cancers Symposium.

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. Fennec Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9658047-en) on February 20, 2026, and is solely responsible for the information contained therein.

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