Rigel Pharmaceuticals, Inc. (NASDAQ:RIGL – Get Free Report) shares hit a new 52-week high during trading on Tuesday after Citigroup raised their price target on the stock from $40.00 to $49.00. Citigroup currently has a buy rating on the stock. Rigel Pharmaceuticals traded as high as $29.82 and last traded at $28.93, with a volume of 329962 shares trading hands. The stock had previously closed at $24.95.
A number of other analysts also recently weighed in on the company. Cantor Fitzgerald reiterated a “neutral” rating and set a $15.00 target price on shares of Rigel Pharmaceuticals in a research report on Friday, September 20th. StockNews.com upgraded Rigel Pharmaceuticals from a “buy” rating to a “strong-buy” rating in a report on Friday, October 18th. Finally, HC Wainwright restated a “buy” rating and issued a $57.00 price objective on shares of Rigel Pharmaceuticals in a report on Friday, October 25th. Two research analysts have rated the stock with a hold rating, two have given a buy rating and one has given a strong buy rating to the company. According to data from MarketBeat.com, Rigel Pharmaceuticals presently has an average rating of “Moderate Buy” and a consensus target price of $33.38.
Check Out Our Latest Stock Report on Rigel Pharmaceuticals
Hedge Funds Weigh In On Rigel Pharmaceuticals
Rigel Pharmaceuticals Stock Up 9.1 %
The stock has a market capitalization of $478.80 million, a PE ratio of 194.44 and a beta of 0.96. The company’s fifty day moving average price is $15.29 and its 200-day moving average price is $12.03.
Rigel Pharmaceuticals Company Profile
Rigel Pharmaceuticals, Inc, a biotechnology company, engages in discovering, developing, and providing therapies that enhance the lives of patients with hematologic disorders and cancer. The company’s commercialized products include Tavalisse, an oral spleen tyrosine kinase inhibitor for the treatment of adult patients with chronic immune thrombocytopenia; Rezlidhia, a non-intensive monotherapy for the treatment of adult patients with relapsed or refractory (R/R) acute myeloid leukemia (AML) with a susceptible isocitrate dehydrogenase-1 (IDH1) mutation as detected by an FDA-approved test; and GAVRETO, a once daily, small molecule, oral, kinase inhibitor for the treatment of adult patients with metastatic rearranged during transfection (RET) fusion-positive non-small cell lung cancer, as well as for the treatment of adult and pediatric patients 12 years of age and older with advanced or metastatic RET fusion-positive thyroid cancer.
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