Taysha Gene Therapies, Inc. (NASDAQ:TSHA – Get Free Report) has been given an average rating of “Buy” by the eight brokerages that are covering the firm, Marketbeat Ratings reports. Eight analysts have rated the stock with a buy rating. The average 1 year price objective among brokers that have issued ratings on the stock in the last year is $6.63.
Several research analysts have recently issued reports on TSHA shares. Cantor Fitzgerald reissued an “overweight” rating and issued a $7.00 target price on shares of Taysha Gene Therapies in a research report on Tuesday, November 12th. Canaccord Genuity Group increased their target price on Taysha Gene Therapies from $6.00 to $8.00 and gave the company a “buy” rating in a research note on Friday, November 15th. Chardan Capital reiterated a “buy” rating and set a $7.00 target price on shares of Taysha Gene Therapies in a research note on Thursday, November 14th. JMP Securities reissued a “market outperform” rating and set a $5.00 price target on shares of Taysha Gene Therapies in a report on Tuesday, November 12th. Finally, Needham & Company LLC reissued a “buy” rating and set a $6.00 price target on shares of Taysha Gene Therapies in a report on Monday, January 6th.
View Our Latest Report on Taysha Gene Therapies
Institutional Investors Weigh In On Taysha Gene Therapies
Taysha Gene Therapies Trading Down 3.2 %
TSHA opened at $1.53 on Monday. The business has a 50 day simple moving average of $2.14 and a two-hundred day simple moving average of $2.11. The firm has a market capitalization of $313.56 million, a price-to-earnings ratio of 2.43 and a beta of 0.95. The company has a debt-to-equity ratio of 0.48, a current ratio of 5.51 and a quick ratio of 5.51. Taysha Gene Therapies has a one year low of $1.19 and a one year high of $4.32.
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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