Wedbush reiterated their outperform rating on shares of TScan Therapeutics (NASDAQ:TCRX – Free Report) in a research note released on Tuesday morning, Benzinga reports. Wedbush currently has a $10.00 price objective on the stock.
Separately, HC Wainwright reiterated a buy rating and issued a $15.00 price target on shares of TScan Therapeutics in a research note on Thursday, March 7th.
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TScan Therapeutics Price Performance
TScan Therapeutics (NASDAQ:TCRX – Get Free Report) last posted its quarterly earnings data on Wednesday, March 6th. The company reported ($0.21) EPS for the quarter, beating the consensus estimate of ($0.29) by $0.08. TScan Therapeutics had a negative net margin of 423.86% and a negative return on equity of 60.65%. The business had revenue of $7.21 million during the quarter, compared to analyst estimates of $2.94 million. As a group, analysts forecast that TScan Therapeutics will post -1.03 EPS for the current year.
Institutional Inflows and Outflows
A number of institutional investors have recently added to or reduced their stakes in TCRX. Letko Brosseau & Associates Inc. purchased a new position in TScan Therapeutics in the third quarter worth approximately $83,000. Pale Fire Capital SE purchased a new position in TScan Therapeutics in the third quarter worth approximately $42,000. abrdn plc purchased a new position in TScan Therapeutics in the fourth quarter worth approximately $1,166,000. Finally, Cannon Global Investment Management LLC purchased a new position in TScan Therapeutics in the first quarter worth approximately $139,000. Hedge funds and other institutional investors own 82.83% of the company’s stock.
About TScan Therapeutics
TScan Therapeutics, Inc, a clinical-stage biopharmaceutical company, develops T cell receptor-engineered T cell (TCR-T) therapies for the treatment of patients with cancer in the United States. The company's lead product candidates include TSC-100 and TSC-101 that is in Phase I clinical trial for the treatment of patients with hematologic malignancies to eliminate residual disease and prevent relapse after allogeneic hematopoietic cell transplantation.
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