Entrada Therapeutics, Inc. (NASDAQ:TRDA – Get Free Report) Director Peter S. Kim bought 2,600 shares of the business’s stock in a transaction dated Monday, April 8th. The shares were bought at an average cost of $13.57 per share, with a total value of $35,282.00. Following the purchase, the director now directly owns 62,936 shares of the company’s stock, valued at $854,041.52. The purchase was disclosed in a document filed with the Securities & Exchange Commission, which is available at this link.
Entrada Therapeutics Stock Up 5.9 %
Entrada Therapeutics stock opened at $13.26 on Friday. The company has a fifty day simple moving average of $13.51 and a 200-day simple moving average of $14.46. Entrada Therapeutics, Inc. has a 52-week low of $10.62 and a 52-week high of $18.44.
Entrada Therapeutics (NASDAQ:TRDA – Get Free Report) last announced its quarterly earnings data on Wednesday, March 13th. The company reported ($0.29) earnings per share (EPS) for the quarter, missing the consensus estimate of ($0.07) by ($0.22). The business had revenue of $41.85 million for the quarter, compared to analysts’ expectations of $27.82 million. Entrada Therapeutics had a negative net margin of 5.18% and a negative return on equity of 2.89%. Equities analysts anticipate that Entrada Therapeutics, Inc. will post -1.54 EPS for the current fiscal year.
Institutional Investors Weigh In On Entrada Therapeutics
Wall Street Analyst Weigh In
TRDA has been the topic of several research analyst reports. HC Wainwright reiterated a “buy” rating and issued a $20.00 price objective on shares of Entrada Therapeutics in a report on Monday, March 18th. Oppenheimer started coverage on Entrada Therapeutics in a research report on Friday, January 5th. They issued an “outperform” rating and a $22.00 target price on the stock.
View Our Latest Analysis on TRDA
Entrada Therapeutics Company Profile
Entrada Therapeutics, Inc, a clinical-stage biotechnology company, develops endosomal escape vehicle (EEV) therapeutics for the treatment of multiple neuromuscular diseases. Its EEV platform develops a portfolio of oligonucleotide, antibody, and enzyme-based programs. Its therapeutic candidates, which include ENTR-601-44, which is in Phase I clinical trial for the treatment of Duchenne muscular dystrophy; and ENTR-701, which is in Phase 1/2 clinical trial for the treatment of myotonic dystrophy type 1.
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