MARKET

DSGN

DSGN

Design Therapeutics, Inc.
NASDAQ
10.53
-0.18
-1.68%
After Hours: 10.53 0 0.00% 16:10 03/27 EDT
OPEN
10.68
PREV CLOSE
10.71
HIGH
10.80
LOW
10.33
VOLUME
184.54K
TURNOVER
--
52 WEEK HIGH
11.23
52 WEEK LOW
2.600
MARKET CAP
649.41M
P/E (TTM)
-8.6496
1D
5D
1M
3M
1Y
5Y
1D
Weekly Report: what happened at DSGN last week (0316-0320)?
Weekly Report · 4d ago
Design Therapeutics Price Target Announced at $15.00/Share by Jefferies
Dow Jones · 03/16 13:17
Jefferies Initiates Coverage On Design Therapeutics with Buy Rating, Announces Price Target of $15
Benzinga · 03/16 13:16
Weekly Report: what happened at DSGN last week (0309-0313)?
Weekly Report · 03/16 10:00
U.S. RESEARCH ROUNDUP-Alnylam Pharmaceuticals, Cogent Biosciences, Summit Therapeutics
Reuters · 03/16 10:00
DESIGN THERAPEUTICS INC <DSGN.O>: JEFFERIES INITIATES COVERAGE WITH BUY RATING; PRICE TARGET $15
Reuters · 03/16 08:20
Design Therapeutics (DSGN) Receives a New Rating from a Top Analyst
TipRanks · 03/16 00:36
Design Therapeutics initiated with a Buy at Jefferies
TipRanks · 03/16 00:15
More
About DSGN
Design Therapeutics, Inc. is a biotechnology company. It is engaged in the research and development of GeneTACT molecules, which are 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 Friedreich ataxia (FA) program is focused on the development of a disease-modifying treatment. Its DT-216 is developed to overcome the FXN transcription impairment that causes FA. DT-216 is in Phase I clinical trial. It is also engaged in developing DT-216 to enable higher exposure and chronic administration for treatment of FA, known as DT-216P2, which uses the same drug substance, DT-216. Its FECD program is focused on the development of a potentially disease-modifying medical treatment for FECD, DT-168, which is in Phase I clinical trial. Its Huntington's Disease program is focused on the development of a potentially disease-modifying treatment for HD.

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