Medicus Pharma Ltd. 宣布，其用于治疗伴有高心血管风险的晚期前列腺癌患者的Teverelix® IIb期临床试验，已获得美国食品药品监督管理局（FDA）的“研究可继续进行”许可。这一监管里程碑意味着公司可以按计划推进该临床阶段的研究工作。
Medicus Pharma Ltd. 宣布，其用于治疗伴有高心血管风险的晚期前列腺癌患者的Teverelix® IIb期临床试验，已获得美国食品药品监督管理局（FDA）的“研究可继续进行”许可。这一监管里程碑意味着公司可以按计划推进该临床阶段的研究工作。
Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.