Asieris Pharmaceuticals Receives NMPA Approval for Hexvix (APL-1706) in Bladder Cancer Diagnosis

Asieris Pharmaceuticals Receives NMPA Approval for Hexvix (APL-1706) in Bladder Cancer Diagnosis

China-based urogenital cancer specialist Asieris Pharmaceuticals (SHA: 688176) has announced that the National Medical Products Administration (NMPA) has approved a marketing filing for its product Hexvix (APL-1706), which is used in the diagnosis and management of bladder cancer.

Product Approval and Impact
The approval of Hexvix by the NMPA marks a significant milestone for Asieris Pharmaceuticals, as Hexvix, with hexaminolevulinate (HAL) as its active ingredient, is the only approved agent globally for assisting in the diagnosis or surgery of bladder cancer. The product has the potential to significantly improve the detection rate of non-muscle invasive bladder cancer (NMIBC) when used in conjunction with blue light cystoscopy.

Enhancing Diagnostic Capabilities
The use of Hexvix in combination with blue light cystoscopy provides a more effective method for detecting bladder cancer, particularly NMIBC, which is a critical aspect of patient care and treatment planning. This approval not only expands the available diagnostic tools for urogenital cancer specialists in China but also highlights Asieris Pharmaceuticals’ commitment to advancing cancer diagnostics and treatment.- Flcube.com

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