Maxim Group Analysts Give BeyondSpring (BYSI) a $52.00 Price Target

Maxim Group set a $52.00 price objective on BeyondSpring (NASDAQ:BYSI) in a report issued on Thursday morning. The firm currently has a buy rating on the stock.

A number of other brokerages have also recently commented on BYSI. HC Wainwright restated a buy rating and issued a $50.00 price target on shares of BeyondSpring in a research report on Monday, August 21st. Zacks Investment Research cut BeyondSpring from a hold rating to a sell rating in a research report on Monday, November 13th.

Shares of BeyondSpring (BYSI) traded up $0.06 on Thursday, reaching $32.57. The company’s stock had a trading volume of 43 shares, compared to its average volume of 1,300. BeyondSpring has a fifty-two week low of $16.55 and a fifty-two week high of $48.49.

BeyondSpring (NASDAQ:BYSI) last issued its quarterly earnings results on Thursday, November 9th. The company reported ($0.68) EPS for the quarter, topping analysts’ consensus estimates of ($0.69) by $0.01. sell-side analysts expect that BeyondSpring will post -4.41 EPS for the current year.

An institutional investor recently bought a new position in BeyondSpring stock. Tanaka Capital Management Inc. acquired a new position in BeyondSpring Inc. (NASDAQ:BYSI) in the second quarter, according to the company in its most recent disclosure with the Securities & Exchange Commission. The institutional investor acquired 21,322 shares of the company’s stock, valued at approximately $914,000. BeyondSpring accounts for approximately 2.1% of Tanaka Capital Management Inc.’s portfolio, making the stock its 16th largest holding. Tanaka Capital Management Inc. owned 0.10% of BeyondSpring at the end of the most recent reporting period. 1.22% of the stock is currently owned by hedge funds and other institutional investors.

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BeyondSpring Company Profile

BeyondSpring Inc is a global clinical-stage biopharmaceutical company. The Company is focused on the development of cancer therapies. The Company is engaged in advancing its lead product, Plinabulin, into a Phase II/III clinical trial for the reduction of docetaxel chemotherapy-induced severe, grade 4 neutropenia; a Phase II/III clinical trial for the prevention of non-docetaxel chemotherapy-induced severe, grade 4 neutropenia, and a Phase III clinical trial as an anticancer agent in combination with docetaxel in advanced non-small cell lung cancer (NSCLC).

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