Taysha Gene Therapies, Inc. (NASDAQ:TSHA – Get Free Report) has received an average recommendation of “Buy” from the eight analysts that are currently covering the company, Marketbeat Ratings reports. Eight research analysts have rated the stock with a buy recommendation. The average 1-year price target among analysts that have covered the stock in the last year is $6.63.
Several research analysts recently weighed in on the company. Chardan Capital reaffirmed a “buy” rating and issued a $7.00 target price on shares of Taysha Gene Therapies in a research report on Wednesday, February 26th. Needham & Company LLC reissued a “buy” rating and issued a $6.00 price objective on shares of Taysha Gene Therapies in a report on Thursday, February 27th.
Read Our Latest Research Report on TSHA
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Taysha Gene Therapies Stock Performance
Shares of TSHA opened at $1.20 on Friday. The company’s fifty day moving average is $1.60 and its two-hundred day moving average is $1.85. Taysha Gene Therapies has a 1 year low of $1.05 and a 1 year high of $4.32. The stock has a market capitalization of $246.00 million, a P/E ratio of 1.90 and a beta of 0.96. The company has a debt-to-equity ratio of 0.48, a quick ratio of 5.51 and a current ratio of 5.51.
Taysha Gene Therapies (NASDAQ:TSHA – Get Free Report) last announced its quarterly earnings results on Wednesday, February 26th. The company reported ($0.07) earnings per share (EPS) for the quarter, beating the consensus estimate of ($0.08) by $0.01. Taysha Gene Therapies had a negative net margin of 229.67% and a negative return on equity of 106.36%. The company had revenue of $2.02 million for the quarter, compared to the consensus estimate of $2.05 million. On average, sell-side analysts predict that Taysha Gene Therapies will post -0.35 earnings per share for the current year.
About Taysha Gene Therapies
Taysha Gene Therapies, Inc, a gene therapy company, focuses on developing and commercializing adeno-associated virus-based gene therapies for the treatment of monogenic diseases of the central nervous system. It primarily develops TSHA-120 for the treatment of giant axonal neuropathy; TSHA-102 for the treatment of Rett syndrome; TSHA-121 for the treatment of CLN7 disease; TSHA-118 for the treatment of CLN1 disease; TSHA-105 for the treatment of for SLC13A5 deficiency; TSHA-113 for the treatment of tauopathies; TSHA-106 for the treatment of angelman syndrome; TSHA-114 for the treatment of fragile X syndrome; and TSHA-101 for the treatment of GM2 gangliosidosis.
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