Entrada Therapeutics, Inc. (NASDAQ:TRDA – Get Free Report) has been assigned an average rating of “Moderate Buy” from the six analysts that are covering the stock, MarketBeat.com reports. One analyst has rated the stock with a sell rating, one has assigned a hold rating, three have given a buy rating and one has issued a strong buy rating on the company. The average twelve-month price target among brokerages that have covered the stock in the last year is $25.6667.
Several research firms have recently issued reports on TRDA. Weiss Ratings reiterated a “sell (d-)” rating on shares of Entrada Therapeutics in a research note on Wednesday, October 8th. Zacks Research upgraded Entrada Therapeutics to a “hold” rating in a research note on Friday, August 8th. Finally, Wall Street Zen downgraded Entrada Therapeutics from a “hold” rating to a “sell” rating in a research note on Saturday, August 9th.
Read Our Latest Analysis on TRDA
Institutional Trading of Entrada Therapeutics
Entrada Therapeutics Stock Performance
Shares of NASDAQ TRDA opened at $6.95 on Wednesday. The stock has a market cap of $264.38 million, a price-to-earnings ratio of -3.90 and a beta of -0.11. The business has a 50 day simple moving average of $5.84 and a 200 day simple moving average of $6.76. Entrada Therapeutics has a 52 week low of $4.93 and a 52 week high of $21.79.
Entrada Therapeutics (NASDAQ:TRDA – Get Free Report) last released its quarterly earnings results on Wednesday, August 6th. The company reported ($1.04) earnings per share (EPS) for the quarter, missing the consensus estimate of ($0.86) by ($0.18). The company had revenue of $1.98 million for the quarter, compared to the consensus estimate of $8.17 million. Entrada Therapeutics had a negative return on equity of 17.81% and a negative net margin of 92.30%. On average, analysts predict that Entrada Therapeutics will post 1.12 EPS for the current year.
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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