ArriVent BioPharma, Inc. (NASDAQ:AVBP – Get Free Report) has been given an average rating of “Moderate Buy” by the ten analysts that are covering the company, Marketbeat.com reports. One investment analyst has rated the stock with a sell recommendation, one has issued a hold recommendation and eight have issued a buy recommendation on the company. The average 12-month price target among analysts that have issued a report on the stock in the last year is $44.8571.
AVBP has been the topic of several recent analyst reports. Weiss Ratings restated a “sell (d-)” rating on shares of ArriVent BioPharma in a report on Friday, July 17th. BTIG Research reissued a “buy” rating and set a $42.00 target price on shares of ArriVent BioPharma in a research report on Thursday, August 13th. HC Wainwright boosted their target price on shares of ArriVent BioPharma from $44.00 to $47.00 and gave the stock a “buy” rating in a research report on Monday, August 17th. Guggenheim restated a “buy” rating and set a $45.00 price target on shares of ArriVent BioPharma in a research note on Thursday, August 13th. Finally, Cantor Fitzgerald reaffirmed an “overweight” rating on shares of ArriVent BioPharma in a report on Friday, May 22nd.
View Our Latest Report on AVBP
Hedge Funds Weigh In On ArriVent BioPharma
ArriVent BioPharma Price Performance
Shares of NASDAQ:AVBP opened at $30.17 on Thursday. The business’s 50-day moving average is $31.62 and its 200 day moving average is $28.35. ArriVent BioPharma has a 1 year low of $17.00 and a 1 year high of $35.83. The firm has a market capitalization of $1.49 billion, a P/E ratio of -8.33 and a beta of 1.36.
ArriVent BioPharma (NASDAQ:AVBP – Get Free Report) last issued its quarterly earnings results on Wednesday, August 12th. The company reported ($1.05) earnings per share for the quarter, missing the consensus estimate of ($0.99) by ($0.06). On average, analysts expect that ArriVent BioPharma will post -4.01 EPS for the current year.
ArriVent BioPharma Company Profile
ArriVent BioPharma, Inc operates as a clinical-stage biopharmaceutical company that engages in the identification, development, and commercialization of medicines for the unmet medical needs of patients with cancers in the United States. It also engages in the development and commercialization of targeted cancer therapies for non-small cell lung cancer (NSCLC) and other solid tumors. In addition, the company develops Furmonertinib, a third-generation tyrosine kinase inhibitor that is in multiple clinical trials across a range of epidermal growth factor receptor mutations (EFGRm) in non-small cell lung cancer (NSCLC), including a phase 3 clinical trial for treatment of patients with metastatic EFGRm NSCLC; phase 1b clinical trial for treatment of patients with NSCLC with other EGFR mutations and NSCLC with HER2 Exon 20 insertion mutations; and ARR-002.
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