Raymond James Financial Inc. acquired a new position in InflaRx (NASDAQ:IFRX – Free Report) during the fourth quarter, according to its most recent filing with the Securities and Exchange Commission (SEC). The fund acquired 638,092 shares of the company’s stock, valued at approximately $1,576,000. Raymond James Financial Inc. owned 1.08% of InflaRx as of its most recent filing with the Securities and Exchange Commission (SEC).
InflaRx Stock Performance
NASDAQ IFRX opened at $1.05 on Wednesday. InflaRx has a twelve month low of $1.01 and a twelve month high of $2.82. The stock has a market cap of $70.49 million, a PE ratio of -0.97 and a beta of 1.98. The firm has a 50-day simple moving average of $1.77 and a 200 day simple moving average of $1.89.
InflaRx (NASDAQ:IFRX – Get Free Report) last announced its quarterly earnings data on Thursday, March 20th. The company reported ($0.09) EPS for the quarter, topping analysts’ consensus estimates of ($0.27) by $0.18. InflaRx had a negative return on equity of 65.98% and a negative net margin of 33,362.70%. Research analysts forecast that InflaRx will post -1.04 earnings per share for the current fiscal year.
Analyst Upgrades and Downgrades
View Our Latest Stock Analysis on IFRX
About InflaRx
InflaRx N.V., a clinical-stage biopharmaceutical company, discovers and develops inhibitors using C5a technology in Germany and the United States. The company's C5a is an inflammatory mediator that is involved in the progression of a variety of autoimmune and other inflammatory diseases. Its lead product candidate is vilobelimab, a novel intravenously delivered first-in-class anti-C5a monoclonal antibody, which completed the Phase III clinical trial for the treatment of hidradenitis suppurativa, a rare and chronic debilitating systemic inflammatory skin disease; for the treatment of anti-neutrophil cytoplasm antibody associated vasculitis, a rare and life-threatening autoimmune disease that is in Phase II trial; to treat pyoderma gangraenosum, a chronic inflammatory skin disorder that is in Phase IIa exploratory study; and for the treatment of PD-1/PD-L1 inhibitor resistant/refractory locally advanced or metastatic cutaneous squamous cell carcinoma that is in Phase II clinical development stage.
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