MARKET

EWTX

EWTX

Edgewise Therapeutics, Inc.
NASDAQ
16.11
+0.46
+2.94%
After Hours: 16.11 0 0.00% 16:20 04/24 EDT
OPEN
15.65
PREV CLOSE
15.65
HIGH
16.33
LOW
15.60
VOLUME
526.41K
TURNOVER
0
52 WEEK HIGH
20.69
52 WEEK LOW
5.12
MARKET CAP
1.50B
P/E (TTM)
-10.2494
1D
5D
1M
3M
1Y
5Y
Edgewise gets EU orphan drug status for muscular dystrophy drug
Edgewise gets EU orphan drug status for muscular dystrophy drug. Edgewise Therapeutics has received orphan drug designation from EU regulators for its drug candidate sevasemten. The drug candidate is in the treatment of Becker muscular dy Strophy and Duchenne muscular dystrophy.
Seeking Alpha · 1d ago
EDGEWISE THERAPEUTICS INC - EMA ORPHAN DRUG DESIGNATIONS FOR SEVASEMTEN (EDG-5506) FOR TREATMENT OF BECKER AND DUCHENNE MUSCULAR DYSTROPHIES
Reuters · 2d ago
Analysts Are Bullish on Top Healthcare Stocks: Biohaven Ltd. (BHVN), Becton Dickinson (BDX)
TipRanks · 2d ago
Edgewise Therapeutics Price Target Raised to $32.00/Share From $28.00 by RBC Capital
Dow Jones · 2d ago
Edgewise Therapeutics Is Maintained at Outperform by RBC Capital
Dow Jones · 2d ago
RBC Capital Maintains Outperform on Edgewise Therapeutics, Raises Price Target to $32
Benzinga · 2d ago
Analysts Anticipate ESML Will Reach $45
NASDAQ · 3d ago
Analysts Are Bullish on These Healthcare Stocks: Bausch + Lomb Corporation (BLCO), Edgewise Therapeutics (EWTX)
TipRanks · 3d ago
More
About EWTX
Edgewise Therapeutics, Inc. is a clinical-stage biopharmaceutical company. It is focused on developing novel therapeutics for muscular dystrophies and serious cardiac conditions. It has built its muscle-focused drug discovery platform. Its platform utilizes custom-built high throughput and translatable systems that measure integrated muscle function in whole organ extracts to identify small molecule precision medicines regulating key proteins in muscle tissue, initially focused on addressing rare neuromuscular and cardiac diseases. Its lead product candidate, EDG-5506, is an orally administered allosteric, selective, fast myofiber (type II) myosin small molecule inhibitor designed to address the root cause of dystrophinopathies, including Duchenne muscular dystrophy and Becker muscular dystrophy. Its product candidate, EDG-7500, for the treatment of hypertrophic cardiomyopathy addition to exploring the potential of its mechanism in the treatment of disorders of diastolic dysfunction.

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