MARKET

DYN

DYN

Dyne Therapeutics, Inc.
NASDAQ
23.86
+0.21
+0.89%
After Hours: 23.68 -0.18 -0.75% 18:28 04/19 EDT
OPEN
23.53
PREV CLOSE
23.65
HIGH
24.21
LOW
23.11
VOLUME
973.26K
TURNOVER
0
52 WEEK HIGH
30.27
52 WEEK LOW
6.40
MARKET CAP
2.06B
P/E (TTM)
-6.0358
1D
5D
1M
3M
1Y
5Y
Notable Friday Option Activity: COIN, SIBN, DYN
NASDAQ · 18h ago
Weekly Report: what happened at DYN last week (0408-0412)?
Weekly Report · 5d ago
Weekly Report: what happened at DYN last week (0401-0405)?
Weekly Report · 04/08 09:02
DYNE THERAPEUTICS INC <DYN.O>: JEFFERIES ASSUMES COVERAGE WITH BUY RATING; TARGET PRICE $36
Reuters · 04/08 05:38
Weekly Report: what happened at DYN last week (0325-0329)?
Weekly Report · 04/01 09:02
Dyne Therapeutics Reports Inducement Grant Under Nasdaq Listing Rule 5635(c)(4) to Newly Appointed President and Chief Executive Officer
Dyne Therapeutics, Inc. Granted an inducement equity award to its newly appointed President and Chief Executive Officer, John G. Cox. The award was approved by the Compensation Committee of Dyne. Dyne is a clinical-stage muscle disease company focused on advancing innovative therapeutics.
Barchart · 03/27 15:05
Dyne Therapeutics Price Target Maintained With a $47.00/Share by Oppenheimer
Dow Jones · 03/26 14:18
Oppenheimer Reiterates Outperform on Dyne Therapeutics, Maintains $47 Price Target
Benzinga · 03/26 14:07
More
About DYN
Dyne Therapeutics Inc. is a clinical-stage muscle disease company. It is focused on advancing life-transforming therapeutics for people living with genetically driven diseases. It is utilizing its FORCE platform to overcome the limitations of muscle tissue delivery and oligonucleotide therapeutics for muscle diseases. Its FORCE platform therapeutics consist of an oligonucleotide payload that is designed to target the genetic basis of the disease. Using its FORCE platform, it is assembling a portfolio of muscle disease therapeutics, including its lead programs in myotonic dystrophy type 1 (DM1), Duchenne muscular dystrophy (DMD), and facioscapulohumeral dystrophy (FSHD). Its therapeutics consist of three components: a Fab, a clinically validated linker, and an oligonucleotide payload that it attaches to its Fab using the linker. It also plans to expand its portfolio through development efforts focused on rare skeletal muscle diseases, as well as cardiac and metabolic muscle diseases.

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