Design Therapeutics, Inc. (DSGN)

NASDAQ: DSGN · Real-Time Price · USD
12.73
+0.20 (1.60%)
Apr 27, 2026, 2:56 PM EDT - Market open
Market Cap785.09M +366.5%
Revenue (ttm)n/a
Net Income-69.79M
EPS-1.22
Shares Out 61.67M
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume193,605
Open12.48
Previous Close12.53
Day's Range12.47 - 13.15
52-Week Range3.11 - 13.54
Beta1.58
AnalystsStrong Buy
Price Target15.25 (+19.8%)
Earnings DateMay 8, 2026

About DSGN

Design Therapeutics, Inc. a clinical-stage biopharmaceutical company, research, designs, develops, and commercializes small molecule therapeutic drugs for the treatment of genetic diseases in the United States. The company utilizes its GeneTAC platform to design and develop therapeutic candidates for inherited diseases caused by nucleotide repeat expansion. Its lead product candidates for potentially disease-modifying treatment comprises Friedreich Ataxia, a monogenic, autosomal recessive, progressive multi-system disease that affects organ sys... [Read more]

Industry Biotechnology
Sector Healthcare
IPO Date Mar 26, 2021
Employees 54
Stock Exchange NASDAQ
Ticker Symbol DSGN
Full Company Profile

Financial Performance

Financial Statements

Analyst Summary

According to 4 analysts, the average rating for DSGN stock is "Strong Buy." The 12-month stock price target is $15.25, which is an increase of 19.80% from the latest price.

Price Target
$15.25
(19.80% upside)
Analyst Consensus: Strong Buy
Stock Forecasts

News

Design Therapeutics Transcript: Leerink Global Healthcare Conference 2026

RESTORE-FA is progressing with key data expected in the second half of the year, while exploratory studies in FECD and DM1 advance using the GeneTAC platform. The company is well-funded into 2029, aiming for clinical proof of concept in major indications.

6 weeks ago - Transcripts

Design Therapeutics Reports Fourth Quarter and Full Year 2025 Financial Results and Recent Business Updates

Trials for DT-216P2 (RESTORE-FA) and DT-168 (FECD) Ongoing; DT-818 (DM1) Dosing in Patients Expected in the First Half of 2026

6 weeks ago - GlobeNewsWire

Design Therapeutics Transcript: Oppenheimer 36th Annual Healthcare Life Sciences Conference

The company presented updates on its small molecule genetic medicine platform, highlighting clinical progress in FA, FECD, and DM1. Key data readouts are expected in the second half of this year and next year, with strong financial resources supporting ongoing trials.

2 months ago - Transcripts

Design Therapeutics to Participate in Upcoming Investor Conferences

CARLSBAD, Calif., Feb. 18, 2026 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, to...

2 months ago - GlobeNewsWire

Design Therapeutics Transcript: Evercore ISI 8th Annual HealthCONx Conference

The company is advancing small molecule therapies for monogenic diseases, with clinical programs in Friedreich's ataxia, Fuchs' corneal dystrophy, and DM1. New formulations have improved safety and exposure, with key data readouts expected in 2026–2027. Cash runway extends into 2029.

5 months ago - Transcripts

Design Therapeutics Transcript: Piper Sandler 37th Annual Healthcare Conference

DT-818 for DM1 will enter clinical trials in 2026, with promising preclinical results and broad tissue targeting. DT-216P2 for FA is off clinical hold, with RESTOR-FA data expected in late 2026, and DT-168 for Fuchs is in a novel biomarker study. Cash runway extends into 2029.

5 months ago - Transcripts

Design Therapeutics Announces Plans to Initiate Patient Dosing of DT-818 in Myotonic Dystrophy Type-1 (DM1) in the First Half of 2026 and Reports Third Quarter 2025 Financial Results

Obtained ex-US Regulatory Clearance for DT-818, a Potentially Best-in-Disease Treatment for Myotonic Dystrophy Type-1 (DM1)  Trials of DT-216P2 in Friedreich Ataxia (FA) and DT-168 in Fuchs Endothelia...

6 months ago - GlobeNewsWire

Design Therapeutics Appoints Justin Gover to Board of Directors

CARLSBAD, Calif., Sept. 10, 2025 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, t...

8 months ago - GlobeNewsWire

Design Therapeutics Transcript: Cantor Global Healthcare Conference 2025

GeneTACs are advancing as selective small molecules for monogenic diseases, with clinical progress in Friedreich's ataxia and Fuchs' corneal dystrophy. Improved formulations and biomarker strategies support ongoing trials, and strong financials enable continued development.

8 months ago - Transcripts

Design Therapeutics to Participate in the 2025 Cantor Global Healthcare Conference

CARLSBAD, Calif., Aug. 27, 2025 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, to...

8 months ago - GlobeNewsWire

Design Therapeutics Highlights Progress Across Lead GeneTAC® Programs and Reports Second Quarter 2025 Financial Results

Early Human Pharmacokinetics Data for DT-216P2 Demonstrates Favorable Translation from Non-Human Primates (NHPs) to Humans and Improved DT-216 Product Profile for Friedreich Ataxia (FA) Program

9 months ago - GlobeNewsWire

Design Therapeutics Transcript: Jefferies Global Healthcare Conference 2025

The company is advancing a differentiated small molecule genomic medicine platform with clinical programs in Friedreich ataxia and Fuchs endothelial corneal dystrophy. New formulations address prior safety and exposure issues, with key data readouts expected in 2026.

11 months ago - Transcripts

Design Therapeutics Announces Start of Friedreich Ataxia Patient Dosing Ex-U.S. in its RESTORE-FA Phase 1/2 Multiple-Ascending Dose Trial of DT-216P2

Initial Data from the Ongoing, Blinded Phase 1 Single-Ascending Dose Trial Has Demonstrated Favorable Safety and Pharmacokinetics IND Application Submitted to Expand RESTORE-FA Trial to U.S. Sites; No...

11 months ago - GlobeNewsWire

Design Therapeutics to Participate in 2025 Jefferies Global Healthcare Conference

CARLSBAD, Calif., May 28, 2025 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, tod...

11 months ago - GlobeNewsWire

Design Therapeutics Transcript: RBC Capital Markets Global Healthcare Conference 2025

Gene tag molecules offer a novel approach to modulate gene expression for monogenic diseases, with lead programs DT-216P2 for Friedreich's ataxia and DT-168 for Fuchs' corneal dystrophy advancing in clinical development. Additional pipeline assets target Huntington's and myotonic dystrophy.

1 year ago - Transcripts

Design Therapeutics to Participate in 2025 RBC Capital Markets Healthcare Conference

CARLSBAD, Calif., May 13, 2025 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, tod...

1 year ago - GlobeNewsWire

Design Therapeutics Highlights Momentum Across Lead GeneTAC® Programs and Reports First Quarter 2025 Financial Results

Phase 1 Single Ascending Dose Trial of DT-216P2 for Friedreich Ataxia (FA) Program Ongoing Reported Favorable Phase 1 Data for DT-168 for Fuchs Endothelial Corneal Dystrophy  (FECD) Program Well-Capit...

1 year ago - GlobeNewsWire

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

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

1 year ago - GlobeNewsWire

Design Therapeutics to Present Phase 1 Data for Fuchs Endothelial Corneal Dystrophy Program at Eyecelerator @ Park City 2025

CARLSBAD, Calif., April 21, 2025 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, t...

1 year ago - GlobeNewsWire

Design Therapeutics Appoints Veteran Industry Executive Chris Storgard, M.D., as Chief Medical Officer

CARLSBAD, Calif., April 17, 2025 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, t...

1 year ago - GlobeNewsWire

Design Therapeutics Transcript: Leerink’s Global Healthcare Conference 2025

Multiple gene-targeted programs are advancing, with a new DT-216P2 formulation for Friedreich ataxia addressing prior limitations and aiming for patient studies in mid-2025. Fuchs program phase I data is expected soon, and strong cash reserves support progress into 2029.

1 year ago - Transcripts

Design Therapeutics Highlights Progress Across Lead GeneTAC® Programs and Reports Fourth Quarter and Full Year 2024 Financial Results

Initiated Phase 1 Single Ascending Dose Trial of DT-216P2 in Healthy Volunteers; Friedreich Ataxia (FA) Patient Dosing to Begin in mid-2025

1 year ago - GlobeNewsWire

Design Therapeutics to Participate in Leerink's Global Healthcare Conference

CARLSBAD, Calif., March 03, 2025 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, t...

1 year ago - GlobeNewsWire

Design Therapeutics Transcript: Piper Sandler 36th Annual Healthcare Conference

DT-216 v2 is set for healthy volunteer studies in early 2025, aiming to address prior safety and exposure issues in FA. The Fuchs program advances with a novel eyedrop and a large observational study, targeting a major unmet need. Both programs are positioned for key data and phase 2 planning in 2025.

1 year ago - Transcripts

Design Therapeutics Transcript: Jefferies London Healthcare Conference 2024

The company is advancing a differentiated genomic medicine platform with four lead programs targeting severe monogenic diseases. Clinical trials for FECD and FA are planned for 2025, supported by a strong cash position and a focus on rapid patient impact.

1 year ago - Transcripts