Hansoh Pharmaceutical: Xinyue®'s third indication approved and launched for the treatment of adult patients with generalized myasthenia gravis

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On March 27, Hansoh Pharmaceutical Group Co., Ltd. announced that its innovative drug Xinyue® (inelizumab injection) received a drug registration certificate issued by the National Medical Products Administration (NMPA), approving an additional indication: this product, in combination with conventional therapeutic drugs, is indicated for the treatment of adult patients with generalized myasthenia gravis (gMG) who are positive for anti-acetylcholine receptor (AChR) antibodies or anti-muscle-specific tyrosine kinase (MuSK) antibodies.

Previously, Xinyue® had already been approved for the treatment of two rare diseases: neuromyelitis optica spectrum disorder (NMOSD) and immunoglobulin G4-related disease (IgG4-RD). This approval of gMG is the third rare-disease indication for Xinyue® that has been approved in China.

(Hansoh Pharmaceutical announcement)

(Edited by: Yang Yan, Lin Chen)

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