Dyne Therapeutics shares rise after positive trial results.
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 08 Dec 25
Source: MarketWatch
Dyne Therapeutics Inc shares increased by 15.61%, crossing above the 5-day SMA, following the announcement of positive topline results from the Phase 1/2 DELIVER trial of z-rostudirsen.
The trial demonstrated significant improvements in dystrophin expression and functional outcomes for patients with Duchenne muscular dystrophy. This positive data is expected to enhance the company's market position and investor confidence.
With plans to submit a Biologics License Application in Q2 2026 and initiate a global Phase 3 study, Dyne Therapeutics is positioning itself for a potential U.S. launch in early 2027, indicating strong future growth prospects.
Analyst Views on DYN
Wall Street analysts forecast DYN stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for DYN is 38.40 USD with a low forecast of 17.00 USD and a high forecast of 60.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
10 Analyst Rating
8 Buy
2 Hold
0 Sell
Strong Buy
Current: 17.700
Low
17.00
Averages
38.40
High
60.00
Current: 17.700
Low
17.00
Averages
38.40
High
60.00
About DYN
Dyne Therapeutics, Inc. is a clinical-stage neuromuscular disease company. It is discovering and advancing therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE platform, it is developing targeted therapeutics that deliver to muscle and the central nervous system (CNS). It has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. Its product candidate, DYNE-101, is being evaluated in ACHIEVE, an ongoing Phase I/II global clinical trial in patients with DM1. Its product candidate, DYNE-251, is being evaluated in DELIVER, an ongoing Phase I/II global clinical trial in patients with DMD who have mutations amenable to exon 51 skipping. Its other product candidates are DYNE-302 and DYNE-401. DYNE-302 addresses the genetic basis of FSHD.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
