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Design Therapeutics, Inc. (DSGN)

NasdaqGS - NasdaqGS Real-time price. Currency in USD
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4.6250-0.1450 (-3.04%)
As of 03:42PM EDT. Market open.
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Trade prices are not sourced from all markets
Previous close4.7700
Open4.7700
Bid4.6200 x 100
Ask4.6300 x 100
Day's range4.6000 - 4.8900
52-week range1.9400 - 8.3100
Volume177,801
Avg. volume314,306
Market cap261.289M
Beta (5Y monthly)1.84
PE ratio (TTM)N/A
EPS (TTM)N/A
Earnings dateN/A
Forward dividend & yieldN/A (N/A)
Ex-dividend dateN/A
1y target estN/A
  • GlobeNewswire

    Design Therapeutics Announces First Quarter 2024 Financial Results and Highlights Upcoming Program Milestones

    Advancing DT-216P2, New Drug Product for Friedreich Ataxia (FA), Toward Clinical Trials Starting Phase 1 Development for Fuchs Endothelial Corneal Dystrophy (FECD) in 2024; Observational Study Currently Enrolling Patients Progressing GeneTACTM Pipeline Programs in Huntington’s Disease (HD) and Myotonic Dystrophy Type-1 (DM1) to Development Candidates Cash and Securities of $270.7 Million Support Multi-Year Operating Runway and Advancement of Up to Four Programs to Clinical Proof-of-Concept CARLS

  • GlobeNewswire

    Design Therapeutics to Participate in the 2024 RBC Capital Markets Global Healthcare Conference

    CARLSBAD, Calif., May 07, 2024 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a biotechnology company developing treatments for serious degenerative genetic diseases, today announced that management will participate in a fireside chat at the 2024 RBC Capital Markets Healthcare Conference on Wednesday, May 15, 2024, at 11:30 a.m. ET in New York. A live webcast of the fireside chat will be available here and in the investors section of the company’s website at www.designtx.com. The

  • GlobeNewswire

    Design Therapeutics Outlines Progress Across GeneTAC™ Platform and Announces Fourth Quarter and Full Year 2023 Financial Results

    New Drug Product for Friedreich Ataxia (FA) DT-216P2 with Favorable Nonclinical Pharmacokinetic and Injection Site Safety Profile; Complete GLP Studies by Year-end 2024 to Start Patient Trials in 2025 IND Cleared for DT-168 for Treatment of Fuchs Endothelial Corneal Dystrophy (FECD) with Phase 1 Development to Start in 2024; Observational Study Underway to Confirm Patient Characteristics and Evaluate Potential Endpoints New Program Unveiled for Huntington’s Disease (HD) Targeting Reduction of Mu