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Design Therapeutics/$DSGN

1D1W1M3M6MYTD1Y5YMAX

About Design Therapeutics

Design Therapeutics Inc is a clinical-stage biopharmaceutical company pioneering the research and development of GeneTAC molecules, which are a novel class of 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 pipeline includes Friedreich Ataxia, FECD, DM1, and Huntington's Disease. The company operates in one operating and reportable segment focused on utilizing the company's proprietary GeneTAC platform to design and develop therapeutic candidates for inherited diseases driven by nucleotide repeat expansion.
Ticker
$DSGN
Sector
Health
Primary listing
NASDAQ
Employees
55

DSGN Metrics

BasicAdvanced
$635M
-
-$1.18
1.64
-

What the Analysts think about DSGN

Analyst ratings (Buy, Hold, Sell) for Design Therapeutics stock.
Analyst projections of the future price of Design Therapeutics stock.

Bulls say / Bears say

DT-216P2 produced a promising early signal in Friedreich ataxia: after four weeks, the highest-dose cohort showed higher frataxin measures in blood and muscle alongside improvements in movement and fatigue scores. The drug was generally well tolerated, supporting further testing. (SEC)
The company had $207.4 million in cash and investments at the end of June 2026, which it said would cover anticipated needs for more than 12 months. That gives it room to advance clinical work before needing new funding. (SEC)
Design has moved beyond its lead programme: it has begun dosing patients in a Phase 1 trial of DT-818 for myotonic dystrophy type 1, while its Phase 2 DT-168 study for Fuchs dystrophy is ongoing. Positive results could show that the GeneTAC approach has value across more than one disease. (GlobeNewswire)
The encouraging clinical changes came from only four patients at the highest dose, after four weeks, in an early study. These exploratory results may not be sustained or reproduced in a larger, longer trial. (SEC)
The next-stage plan relies on blood frataxin as the primary efficacy measure, but the company is still seeking FDA feedback on whether it could support a faster approval route. If regulators do not accept that measure as a suitable surrogate, development may need to rely on clinical outcomes and take longer. (StockAnalysis)
The Fuchs dystrophy study’s data have slipped to 2027 because of a delay in supplies for the eye-drop formulation, while the first patient data from the myotonic dystrophy programme are also not expected until 2027. Those delays push back evidence for the company’s broader pipeline. (GlobeNewswire)
Data summarised monthly by Lightyear AI. Last updated on 17 Oct 2026.

DSGN Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

DSGN Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

Funds containing DSGN

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