Design Therapeutics, Inc. (DSGN)

US — Healthcare Sector
Peers: EWTX  TRML  ACET  CGEM  VOR  IMCR 

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Key Metrics & Ratings

  • symbol DSGN
  • Rev/Share 0.0103
  • Book/Share 3.7467
  • PB 1.3745
  • Debt/Equity 0.0052
  • CurrentRatio 25.1279
  • ROIC -0.3485

 

  • MktCap 293282715.0
  • FreeCF/Share -0.8931
  • PFCF -5.7757
  • PE -4.6123
  • Debt/Assets 0.0049
  • DivYield 0
  • ROE -0.2715

 

  • Rating B-
  • Score 2
  • Recommendation Sell
  • P/E Score 1
  • DCF Score 3
  • P/B Score 4
  • D/E Score 4

Recent Analyst Ratings

Type Ticker Analyst Firm Previous Rating Current Rating Previous Price Target Current Price Target Date
No ratings available.

News

Design Therapeutics Announces Favorable Phase 1 Data for DT-168 Supporting Advancement into Phase 2 Biomarker Trial for Patients with Fuchs Endothelial Corneal Dystrophy
DSGN
Published: May 01, 2025 by: GlobeNewsWire
Sentiment: Neutral

Phase 2 biomarker trial in FECD patients anticipated to begin in the second half of 2025 Phase 2 biomarker trial in FECD patients anticipated to begin in the second half of 2025

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image for news Design Therapeutics Announces Favorable Phase 1 Data for DT-168 Supporting Advancement into Phase 2 Biomarker Trial for Patients with Fuchs Endothelial Corneal Dystrophy

About Design Therapeutics, Inc. (DSGN)

  • IPO Date 2021-03-29
  • Website https://www.designtx.com
  • Industry Biotechnology
  • CEO Pratik Shah
  • Employees 56

Design Therapeutics, Inc. a preclinical-stage biopharmaceutical company, engages in the development of therapies for the treatment of genetic diseases caused by nucleotide repeat expansions. The company's portfolio of products comprises Friedreich Ataxia, a monogenic, autosomal recessive, progressive multi-system disease that affects organ systems dependent on mitochondrial function, eventually leading to neurological, cardiac, and metabolic dysfunction; and Myotonic Dystrophy Type-1 (DM1), a dominantly-inherited, monogenic progressive neuromuscular disease affecting skeletal muscle, heart, brain, and other organs. It is also developing GeneTAC product candidate portfolio for the treatment of other nucleotide repeat expansion-driven monogenic diseases, such as Fragile X syndrome, spinocerebellar ataxias, amyotrophic lateral sclerosis, frontotemporal dementia, Huntington disease, and spinobulbar muscular atrophy. Design Therapeutics, Inc. was incorporated in 2017 and is headquartered in Carlsbad, California.