Hinova Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of innovative small-molecule therapeutics and targeted protein degraders for the treatment of oncology and metabolic diseases. Founded in 2013 and headquartered in Chengdu, China, the company operates research, development, and clinical management facilities across Chengdu, Beijing, and the United States. Hinova Pharmaceuticals leverages proprietary drug discovery engines, including a targeted protein degradation (PROTAC) platform and a deuterated drug technology platform. The company's therapeutic pipeline comprises HC-1119, an oral deuterated androgen receptor antagonist developed for metastatic castration-resistant prostate cancer (mCRPC); HP518, an orally bioavailable PROTAC androgen receptor degrader targeting advanced and drug-resistant prostate cancer; HP501, a selective uric acid transporter 1 (URAT1) inhibitor indicated for hyperuricemia and gout; HP551, a next-generation URAT1 inhibitor for metabolic conditions; HP537, a selective p300/CBP histone acetyltransferase inhibitor evaluated for solid tumors and hematological malignancies; and HP560, an oral PROTAC estrogen receptor degrader developed for ER-positive and HER2-negative breast cancer. In recent developments, Hinova Pharmaceuticals submitted a New Drug Application (NDA) to China's National Medical Products Administration (NMPA) for its lead oncology asset HC-1119; accelerated multi-regional Phase I/II clinical trials for HP518 across China, the United States, and Australia following international regulatory clearances; advanced Phase II clinical trials for HP501 in gout and hyperuricemia; and expanded its strategic collaborations and clinical-stage manufacturing infrastructure to support global pipeline commercialization.