Medpace (NASDAQ:MEDP – Get Free Report) is set to release its earnings data after the market closes on Monday, October 21st. Analysts expect Medpace to post earnings of $2.78 per share for the quarter. Medpace has set its FY24 guidance at $11.24-11.93 EPS and its FY 2024 guidance at 11.240-11.930 EPS.Individual that are interested in participating in the company’s earnings conference call can do so using this link.
Medpace (NASDAQ:MEDP – Get Free Report) last released its quarterly earnings results on Monday, July 22nd. The company reported $2.75 earnings per share for the quarter, topping the consensus estimate of $2.54 by $0.21. The company had revenue of $528.10 million for the quarter, compared to analysts’ expectations of $528.41 million. Medpace had a return on equity of 55.14% and a net margin of 16.74%. The business’s quarterly revenue was up 14.6% compared to the same quarter last year. During the same period in the previous year, the business posted $1.93 earnings per share. On average, analysts expect Medpace to post $12 EPS for the current fiscal year and $13 EPS for the next fiscal year.
Medpace Price Performance
Shares of NASDAQ MEDP opened at $356.40 on Friday. Medpace has a 1 year low of $227.21 and a 1 year high of $459.77. The firm has a market cap of $11.04 billion, a PE ratio of 36.33, a price-to-earnings-growth ratio of 1.77 and a beta of 1.35. The company has a 50 day simple moving average of $356.43 and a 200 day simple moving average of $383.50.
Analyst Ratings Changes
View Our Latest Stock Analysis on Medpace
Medpace Company Profile
Medpace Holdings, Inc provides clinical research-based drug and medical device development services in North America, Europe, and Asia. The company offers a suite of services supporting the clinical development process from Phase I to Phase IV in various therapeutic areas. It provides clinical development services to the pharmaceutical, biotechnology, and medical device industries; and development plan design, coordinated central laboratory, project management, regulatory affairs, clinical monitoring, data management and analysis, pharmacovigilance new drug application submissions, and post-marketing clinical support services.
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