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Design Therapeutics Inc

DSGN
查看詳細走勢圖
10.530USD
-0.180-1.68%
收盤 03/27, 16:00美東報價延遲15分鐘
566.70M總市值
虧損本益比TTM

Design Therapeutics Inc

10.530
-0.180-1.68%
盤中分時
1分
30分
1小時
日k
週k
月k
日k

今天

-1.68%

5天

+2.13%

1月

+0.86%

6月

+60.27%

今年開始到現在

+12.26%

1年

+150.12%

查看詳細走勢圖

TradingKey Design Therapeutics Inc股票評分

單位: USD 更新時間: 2026-03-27

操作建議

Design Therapeutics Inc當前公司基本面數據相對謹慎,最新ESG揭露屬於行業領先水平。增長潛力很大。當前估值合理,在生物技術與醫療研究行業排名149/391位。機構持股佔比非常高,近一月多位分析師給出公司評級為強力買入。最高目標價為14.67。中期看,股價處於平穩狀態。近一個月,市場表現一般,但技術面評分較高。目前股價在壓力位和支撐位之間,可以做區間波段操作。

Design Therapeutics Inc評分

相關信息

行業排名
149 / 391
全市場排名
274 / 4542
所屬行業
生物技術與醫療研究

壓力支撐

由於公司未披露,未能獲取相關數據

多維評測

本期評分
上期評分

公司輿情

過去24小時
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Design Therapeutics Inc亮點

亮點風險
Design Therapeutics, Inc. is a biotechnology company. It is engaged in the research and development of GeneTACT molecules, which are small-molecule gene targeted chimera therapeutic candidates designed to be disease-modifying by addressing the underlying cause of diseases caused by inherited nucleotide repeat expansion mutations. Its Friedreich ataxia (FA) program is focused on the development of a disease-modifying treatment. Its DT-216 is developed to overcome the FXN transcription impairment that causes FA. DT-216 is in Phase I clinical trial. It is also engaged in developing DT-216 to enable higher exposure and chronic administration for treatment of FA, known as DT-216P2, which uses the same drug substance, DT-216. Its FECD program is focused on the development of a potentially disease-modifying medical treatment for FECD, DT-168, which is in Phase I clinical trial. Its Huntington's Disease program is focused on the development of a potentially disease-modifying treatment for HD.
估值低估
公司最新PE估值-8.65,處於3年歷史低位
機構減倉
最新機構持股33.55M股,環比減少3.29%
詹姆斯·西蒙斯持倉
明星投資者詹姆斯·西蒙斯持倉,最新持倉287.10K股

分析師目標

基於 6 分析師
強力買入
評級
14.667
目標均價
+36.94%
漲幅空間
數據免責聲明:分析師評級與目標價由LSEG提供,僅供參考,不應當作投資建議

Design Therapeutics Inc新聞

即將為您帶來更多新聞,敬請期待。 。 。

財務指標

每股收益

由於公司未披露,未能獲取相關數據

營業總收入

由於公司未披露,未能獲取相關數據

Design Therapeutics Inc簡介

Design Therapeutics, Inc. is a biotechnology company. It is engaged in the research and development of GeneTACT molecules, which are small-molecule gene targeted chimera therapeutic candidates designed to be disease-modifying by addressing the underlying cause of diseases caused by inherited nucleotide repeat expansion mutations. Its Friedreich ataxia (FA) program is focused on the development of a disease-modifying treatment. Its DT-216 is developed to overcome the FXN transcription impairment that causes FA. DT-216 is in Phase I clinical trial. It is also engaged in developing DT-216 to enable higher exposure and chronic administration for treatment of FA, known as DT-216P2, which uses the same drug substance, DT-216. Its FECD program is focused on the development of a potentially disease-modifying medical treatment for FECD, DT-168, which is in Phase I clinical trial. Its Huntington's Disease program is focused on the development of a potentially disease-modifying treatment for HD.
公司代碼DSGN
公司Design Therapeutics Inc
CEOShah (Pratik)
網址https://www.designtx.com/
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