Biostar Pharma, the US subsidiary of Beijing Biostar Pharmaceuticals Co., Ltd., has announced the initiation of two phase II/III multiregional clinical trials for the Utidelone Capsule (UTD2). The trials focus on the first-line treatment for locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma and the treatment for platinum-resistant advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer. The first patients were dosed on September 11 and September 12, 2025, respectively. Utidelone is noted for its higher oral bioavailability and lower risk of cross-resistance compared to taxanes, which enhances its convenience and potential in combination therapies. The company has not yet presented results from these ongoing trials.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Beijing Biostar Pharmaceuticals Co. Ltd. published the original content used to generate this news brief via PR Newswire (Ref. ID: CN73152) on September 15, 2025, and is solely responsible for the information contained therein.
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