Hearing loss therapy: Fennec Pharma gets USFDA nod for PEDMARK
"The FDA approval of PEDMARK represents an important breakthrough for pediatric patients with localized, non-metastatic solid tumors at risk for cisplatin-induced hearing loss," said Rosty Raykov, chief executive officer of Fennec Pharmaceuticals.;
Research Triangle Park, N.C.: Fennec Pharmaceuticals Inc., a specialty pharmaceutical company, has announced that the U.S. Food and Drug Administration(USFDA) has approved PEDMARK (sodium thiosulfate injection) to reduce the risk of ototoxicity associated with cisplatin in pediatric patients one month of age and older with localized, non-metastatic solid tumors.
This approval makes PEDMARK the first and only treatment approved by the FDA in this area of significant unmet medical need.
"The FDA approval of PEDMARK represents an important breakthrough for pediatric patients with localized, non-metastatic solid tumors at risk for cisplatin-induced hearing loss. Cisplatin is a critical, standard of care agent, used in the treatment of pediatric cancers; however, even though effective, it could be harmful to children, frequently causing permanent and irreversible bilateral hearing loss. With PEDMARK, physicians now have an approved treatment option to reduce the risk of cisplatin-induced hearing loss in pediatric patients," said Rosty Raykov, chief executive officer of Fennec Pharmaceuticals. "We would like to thank the patients, their families, physicians, investigators, employees, consultants and the entire research team at Oregon Health and Science University, who have contributed to the development of PEDMARK."
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