Shares of Design Therapeutics, Inc. (NASDAQ:DSGN – Get Free Report) have earned an average rating of “Moderate Buy” from the eight research firms that are presently covering the stock, Marketbeat Ratings reports. One analyst has rated the stock with a sell rating, six have given a buy rating and one has assigned a strong buy rating to the company. The average 1 year price target among brokerages that have covered the stock in the last year is $16.50.
DSGN has been the subject of several analyst reports. Oppenheimer raised their price target on shares of Design Therapeutics from $18.00 to $21.00 and gave the company an “outperform” rating in a research report on Monday, May 4th. Weiss Ratings reiterated a “sell (d-)” rating on shares of Design Therapeutics in a research note on Monday, April 20th. Wall Street Zen upgraded Design Therapeutics from a “sell” rating to a “hold” rating in a research note on Sunday, May 10th. Piper Sandler reaffirmed an “overweight” rating and set a $20.00 price target on shares of Design Therapeutics in a report on Wednesday, April 29th. Finally, Cantor Fitzgerald began coverage on Design Therapeutics in a report on Tuesday, May 12th. They set an “overweight” rating on the stock.
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Design Therapeutics Stock Performance
NASDAQ:DSGN opened at $12.57 on Friday. The firm has a market cap of $785.12 million, a P/E ratio of -10.47 and a beta of 1.58. Design Therapeutics has a fifty-two week low of $3.76 and a fifty-two week high of $17.25. The firm has a 50-day simple moving average of $12.67 and a two-hundred day simple moving average of $11.51.
Design Therapeutics (NASDAQ:DSGN – Get Free Report) last issued its earnings results on Tuesday, April 28th. The company reported ($0.29) earnings per share (EPS) for the quarter, topping the consensus estimate of ($0.36) by $0.07. On average, equities research analysts predict that Design Therapeutics will post -1.36 EPS for the current year.
Design Therapeutics Company Profile
Design Therapeutics, Inc a biopharmaceutical company, researches, designs, develops, and commercializes small molecule therapeutic drugs for the treatment of genetic diseases in the United States. The company utilizes its GeneTAC platform to design and develop therapeutic candidates for inherited diseases caused by nucleotide repeat expansion. Its lead product candidates for potentially disease-modifying treatment comprises Friedreich Ataxia, a monogenic, autosomal recessive, progressive multi-system disease that affects organ systems dependent on mitochondrial function that brings to neurological, cardiac, and metabolic dysfunction; Myotonic Dystrophy Type-1, a dominantly-inherited, monogenic progressive neuromuscular disease affecting skeletal muscle, heart, brain, and other organs; Fuchs Endothelial Corneal Dystrophy, a genetic eye disease characterized by bilateral degeneration of corneal endothelial cells and progressive loss of vision; and Huntington's Disease, a dominantly inherited, monogenic neurodegenerative disease characterized by movement, cognitive, and psychiatric disorders.
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