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 1.6708
  • Debt/Equity 0.0052
  • CurrentRatio 25.1279
  • ROIC -0.3485

 

  • MktCap 356495106.0
  • FreeCF/Share -0.8931
  • PFCF -7.0205
  • PE -5.6064
  • 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 to Participate in the 2025 Cantor Global Healthcare Conference
DSGN
Published: August 27, 2025 by: GlobeNewsWire
Sentiment: Neutral

CARLSBAD, Calif., Aug. 27, 2025 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, today announced that management will participate in a fireside chat at the 2025 Cantor Global Healthcare Conference on Thursday, September 4, 2025, at 10:55 a.m. ET in New York.

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image for news Design Therapeutics to Participate in the 2025 Cantor Global Healthcare Conference
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.