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Medicus Pharma Ltd.
0.4575
+0.1058
30.08%
盤後:
0.4400
-0.0175
-3.83%
19:59 EDT
成交量:
1,218.51萬
成交額:
520.95萬
市值:
2,592.11萬
市盈率:
-0.17
高:
0.4760
開:
0.3636
低:
0.3636
收:
0.3517
52周最高:
3.69
52周最低:
0.2500
股本:
5,665.82萬
流通股本:
4,882.16萬
量比:
10.03
換手率:
24.96%
股息:
- -
股息率:
- -
每股收益(TTM):
-2.6300
每股收益(LYR):
-2.7356
淨資產收益率:
-2865.18%
總資產收益率:
-278.12%
市淨率:
19.55
市盈率(LYR):
-0.17
資料載入中...
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公告
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沒有相關數據
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新聞
Medicus Pharma宣佈向美國食品藥品監督管理局提交Skinject®用於戈林綜合徵的罕見兒科疾病認定申請
美股速递
·
06/15
Medicus Pharma啓動基於阿聯酋基因組計劃的突破性Teverelix®治療子宮內膜異位症的Precision-E2 IIa期研究
美股速递
·
06/11
Medicus Pharma推進Teverelix®項目進入註冊開發階段,針對高心血管風險前列腺癌患者完成關鍵歐洲提交
美股速递
·
06/08
Medicus Pharma公布預設擴展二期Sknjct-003數據分析結果 顯示顯著劑量效應
美股速递
·
05/06
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Pharma宣佈向美國食品藥品監督管理局提交Skinject®用於戈林綜合徵的罕見兒科疾病認定申請","url":"https://stock-news.laohu8.com/highlight/detail?id=1126634681","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1126634681?lang=zh_tw&edition=fundamental","pubTime":"2026-06-15 19:31","pubTimestamp":1781523074,"startTime":"0","endTime":"0","summary":"Medicus Pharma Ltd.(MDCX)已正式向美国食品药品监督管理局(FDA)提交申请,为其在研产品Skinject®寻求戈林综合征适应症的罕见儿科疾病认定。这一认定若获批准,将有望为患有此种罕见遗传性皮肤疾病的儿童患者带来新的治疗希望,并可能使公司在后续的研发与商业化进程中享有相应的政策激励。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["MDCX","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1103137641","title":"Medicus Pharma啓動基於阿聯酋基因組計劃的突破性Teverelix®治療子宮內膜異位症的Precision-E2 IIa期研究","url":"https://stock-news.laohu8.com/highlight/detail?id=1103137641","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1103137641?lang=zh_tw&edition=fundamental","pubTime":"2026-06-11 19:31","pubTimestamp":1781177506,"startTime":"0","endTime":"0","summary":"Medicus Pharma Ltd. (MDCX) 宣布启动一项具有开创性的Precision-E2 IIa期临床研究,该研究将利用阿联酋基因组计划的数据,评估其候选药物Teverelix®在治疗子宫内膜异位症方面的疗效与安全性。这项研究标志着该公司在精准医疗领域迈出了重要一步,旨在通过基因组信息为患者提供更个体化的治疗方案。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","MDCX"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1110064382","title":"Medicus Pharma推進Teverelix®項目進入註冊開發階段,針對高心血管風險前列腺癌患者完成關鍵歐洲提交","url":"https://stock-news.laohu8.com/highlight/detail?id=1110064382","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1110064382?lang=zh_tw&edition=fundamental","pubTime":"2026-06-08 19:33","pubTimestamp":1780918414,"startTime":"0","endTime":"0","summary":"Medicus Pharma Ltd. 已将其Teverelix项目推进至注册开发阶段,旨在针对伴有高心血管风险的前列腺癌患者。这一进展的关键标志是公司已向欧洲监管机构提交了关键文件。Teverelix项目专注于满足这一特定患者群体的医疗需求,他们因心血管并发症风险较高,在治疗选择上面临更大挑战。下一步,公司将与监管机构密切合作,以确定后续的开发路径。这一战略举措有望为Medicus Pharma在该治疗领域建立重要地位。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","MDCX"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1113733033","title":"Medicus Pharma公布預設擴展二期Sknjct-003數據分析結果 顯示顯著劑量效應","url":"https://stock-news.laohu8.com/highlight/detail?id=1113733033","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1113733033?lang=zh_tw&edition=fundamental","pubTime":"2026-05-06 19:37","pubTimestamp":1778067449,"startTime":"0","endTime":"0","summary":"Medicus Pharma Ltd.最新披露的预设扩展二期临床试验Sknjct-003数据分析结果证实,其研究药物存在明确的剂量-效应关系。该数据进一步验证了治疗方案的有效性,为后续临床开发提供重要依据。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["MDCX","BK4139"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":4,"totalPage":6,"pageCount":1,"totalSize":23,"code":"91000000","status":"200"}],"@#url:\"https://hq.skytigris.cn/market/plate/belongs/MDCX\",params:#limit:6,delay:false,,,undefined,":[]}}