9月15日(周一),药捷安康低开高走涨近50%,创上市以来新高,前7个交易日狂飙逾360%!
消息面上,该公司发布公告称,其核心产品替恩戈替尼(Tinengotinib, TT-00420)联合氟维司群治疗经治失败的激素受体阳性(HR+)且人表皮生长因子受体2阴性或低表达(HER2-)的复发或转移性乳腺癌Ⅱ期临床试验,已于2025年9月10日获得了中国国家药品监督管理局的临床默示许可。
9月15日(周一),药捷安康低开高走涨近50%,创上市以来新高,前7个交易日狂飙逾360%!
消息面上,该公司发布公告称,其核心产品替恩戈替尼(Tinengotinib, TT-00420)联合氟维司群治疗经治失败的激素受体阳性(HR+)且人表皮生长因子受体2阴性或低表达(HER2-)的复发或转移性乳腺癌Ⅱ期临床试验,已于2025年9月10日获得了中国国家药品监督管理局的临床默示许可。
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.