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MorphoSys AG (MOR)

NasdaqGS - NasdaqGS Real Time Price. Currency in USD
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5.45+0.11 (+2.06%)
At close: 03:59PM EDT
5.45 0.00 (0.00%)
After hours: 07:22PM EDT
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Bullishpattern detected
Head and Shoulders Bottom

Head and Shoulders Bottom

Previous Close5.34
Open5.39
Bid2.67 x 1100
Ask5.49 x 800
Day's Range5.38 - 5.49
52 Week Range4.35 - 22.18
Volume25,957
Avg. Volume51,890
Market Cap744.443M
Beta (5Y Monthly)0.88
PE Ratio (TTM)N/A
EPS (TTM)N/A
Earnings DateN/A
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target EstN/A
Fair Value is the appropriate price for the shares of a company, based on its earnings and growth rate also interpreted as when P/E Ratio = Growth Rate. Estimated return represents the projected annual return you might expect after purchasing shares in the company and holding them over the default time horizon of 5 years, based on the EPS growth rate that we have projected.
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  • Motley Fool

    MorphoSys AG (MOR) Q1 2022 Earnings Call Transcript

    My name is Julia Neugebauer, senior director investor relations at MorphoSys, and it is my pleasure to welcome you to our first quarter 2022 financial results conference call. Joining me on the call today are Jean-Paul Kress, chief executive officer; Sung Lee, chief financial officer; Malte Peters, chief research and development officer; and Joe Horvat, U.S. general manager.

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    Wall Street Analysts Believe MorphoSys AG Unsponsored ADR (MOR) Could Rally 213%: Here's is How to Trade

    The mean of analysts' price targets for MorphoSys AG Unsponsored ADR (MOR) points to a 213.4% upside in the stock. While this highly sought-after metric has not proven reasonably effective, strong agreement among analysts in raising earnings estimates does indicate an upside in the stock.

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    MorphoSys-Incyte Partnered Minjuvi Temporarily Approved In Switzerland

    The Swiss agency for therapeutic products has granted temporary approval for MorphoSys AG (NASDAQ: MOR) and Incyte Corp's (NASDAQ: INCY) Minjuvi (tafasitamab) for relapsed or refractory diffuse large B-cell lymphoma (DLBCL). The approval comes for Minjuvi combined with lenalidomide, followed by Minjuvi monotherapy for adult patients, after at least one prior line of systemic therapy, who are not eligible for autologous stem cell transplant (ASCT). The approval is based on the results from the L-

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