Shares of Taysha Gene Therapies, Inc. (NASDAQ:TSHA – Get Free Report) have received an average recommendation of “Buy” from the eight analysts that are presently covering the firm, MarketBeat reports. Eight research analysts have rated the stock with a buy rating. The average 12 month price target among analysts that have updated their coverage on the stock in the last year is $6.63.
A number of brokerages recently issued reports on TSHA. Chardan Capital reiterated a “buy” rating and set a $7.00 price objective on shares of Taysha Gene Therapies in a research note on Wednesday, February 26th. Needham & Company LLC restated a “buy” rating and set a $6.00 price objective on shares of Taysha Gene Therapies in a research report on Thursday, February 27th.
Check Out Our Latest Stock Report on Taysha Gene Therapies
Institutional Trading of Taysha Gene Therapies
Taysha Gene Therapies Stock Down 3.2 %
TSHA opened at $1.22 on Friday. The firm’s 50 day simple moving average is $1.63 and its two-hundred day simple moving average is $1.88. The company has a market capitalization of $250.10 million, a PE ratio of 1.94 and a beta of 0.96. Taysha Gene Therapies has a 1-year low of $1.17 and a 1-year high of $4.32. The company has a current ratio of 5.51, a quick ratio of 5.51 and a debt-to-equity ratio of 0.48.
Taysha Gene Therapies (NASDAQ:TSHA – Get Free Report) last announced its earnings results on Wednesday, February 26th. The company reported ($0.07) EPS for the quarter, topping analysts’ consensus estimates of ($0.08) by $0.01. The company had revenue of $2.02 million for the quarter, compared to analysts’ expectations of $2.05 million. Taysha Gene Therapies had a negative return on equity of 106.36% and a negative net margin of 229.67%. As a group, equities analysts forecast that Taysha Gene Therapies will post -0.35 EPS for the current year.
Taysha Gene Therapies Company Profile
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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