Humanwell Healthcare Initiates Phase IIa Clinical Study for IPF Drug HW021199

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China-based Humanwell Healthcare (Group) Co., Ltd (SHA: 600079) has announced the commencement of a Phase IIa clinical study for its Category 1 chemical drug, HW021199, in the treatment of idiopathic pulmonary fibrosis (IPF). The drug’s target has not been disclosed, other than to note that there is no market-approved product with the same target globally. Currently, only Boehringer Ingelheim’s Ofev (nintedanib) and GNI Group’s Etuary (pirfenidone) are commercially available for IPF treatment.

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Strategic Partnerships and Orphan Drug Developments in China
In a related development, Daewoong Pharmaceutical has partnered with CS Pharmaceuticals to develop and commercialize the PRS inhibitor bersiporocin, an IPF therapy with orphan drug designation and fast-track status in the US, in Greater China. This agreement was established in January of this year. Additionally, Conba’s pirfenidone and Vcanbio Cell & Gene’s VUM02 have received clinical trial approvals for the treatment of IPF in China.-Fineline Info & Tech

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