MorphoSys AG Reports Preliminary Q2 2022 Monjuvi U.S. Sales and Updates Financial Guidance for 2022
MorphoSys AG reported preliminary Q2 2022 U.S. net product sales of Monjuvi amounting to US$ 23.3 million and US$ 41.9 million for the first half of 2022. The company has updated its 2022 financial guidance, projecting Monjuvi net sales between US$ 90 million and US$ 110 million, down from US$ 110 million to US$ 135 million. Additionally, R&D expenses are now estimated at €275 million to €300 million, and SG&A expenses at €150 million to €165 million. Full results will be published on August 3, 2022.
- Preliminary Q2 2022 Monjuvi U.S. net product sales of US$ 23.3 million.
- First half 2022 Monjuvi U.S. net product sales reached US$ 41.9 million.
- Updated financial guidance indicates expected R&D expenses reduction.
- Gross margin for Monjuvi remains stable at 75% to 80%.
- Reduced full-year net product sales guidance from US$ 110-135 million to US$ 90-110 million.
- Increased R&D expenses guidance range from €300-325 million to €275-300 million.
Publication of an inside information according to Article 17 para. 1 of the Regulation (EU) No. 596/2014
- Preliminary Q2 2022 Monjuvi U.S. net product sales of US
$ 23.3 million (€ 21.7 million) - Update of financial guidance ranges for 2022 Monjuvi U.S. net product sales (now US
$ 90 t o US$ 110 million ), R&D expenses (now € 275 to € 300 million) and SG&A expenses (now € 150 to € 165 million)
PLANEGG/MUNICH, GERMANY / ACCESSWIRE / July 26, 2022 / MorphoSys AG (FSE: MOR)(NASDAQ:MOR) announces today an update of its financial guidance for 2022, after preliminary completion of the latest evaluation of MorphoSys' half year 2022 financial performance.
MorphoSys updates its financial guidance based on the preliminary unaudited consolidated results for the first six months 2022 and following the recent licensing agreements with Human Immunology Biosciences, Inc. (HIBio) for felzartamab and MOR210. Preliminary Monjuvi® (tafasitamab-cxix) U.S. Net Product Sales are US
Full Year 2022 Financial Guidance:
Amounts in million
Updated 2022 Financial Guidance
Previous 2022 Financial Guidance
2022 Guidance Insights
Monjuvi U.S. Net Product Sales
US
US
Gross Margin for Monjuvi U.S. Net Product Sales
R&D expenses
€ 275m to 300m
€ 300m to 325m
Reduction in guidance range driven primarily by license agreement for felzartamab to HIBio executed on July 14, 2022.
SG&A expenses
€ 150m to 165m
€ 155m to 170m
Full results will be published on August 3, 2022, followed by a conference call on August 4, 2022.
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END OF AD HOC RELEASE
Information and Explanation of the Issuer to this News:
About MorphoSys
At MorphoSys, we are driven by our mission: More life for people with cancer. As a global commercial-stage biopharmaceutical company, we use groundbreaking science and technologies to discover, develop, and deliver innovative cancer medicines to patients. MorphoSys is headquartered in Planegg, Germany, and has its U.S. operations anchored in Boston, Massachusetts. To learn more, visit us at www.morphosys.com and follow us on Twitter and LinkedIn.
Monjuvi® is a registered trademark of MorphoSys AG.
Forward Looking Statements
This communication contains certain forward-looking statements concerning the MorphoSys group of companies. The forward-looking statements contained herein represent the judgment of MorphoSys as of the date of this release and involve known and unknown risks and uncertainties, which might cause the actual results, financial condition and liquidity, performance or achievements of MorphoSys, or industry results, to be materially different from any historic or future results, financial conditions and liquidity, performance or achievements expressed or implied by such forward-looking statements. In addition, even if MorphoSys' results, performance, financial condition and liquidity, and the development of the industry in which it operates are consistent with such forward-looking statements, they may not be predictive of results or developments in future periods. Among the factors that may result in differences are that MorphoSys' expectations may be incorrect, the inherent uncertainties associated with competitive developments, clinical trial and product development activities and regulatory approval requirements, MorphoSys' reliance on collaborations with third parties, estimating the commercial potential of its development programs and other risks indicated in the risk factors included in MorphoSys' Annual Report on Form 20-F and other filings with the U.S. Securities and Exchange Commission. Given these uncertainties, the reader is advised not to place any undue reliance on such forward-looking statements. These forward-looking statements speak only as of the date of publication of this document. MorphoSys expressly disclaims any obligation to update any such forward-looking statements in this document to reflect any change in its expectations with regard thereto or any change in events, conditions or circumstances on which any such statement is based or that may affect the likelihood that actual results will differ from those set forth in the forward-looking statements, unless specifically required by law or regulation.
For more information, please contact:
Dr. Julia Neugebauer
Senior Director Investor Relations
Tel: +49 (0)89 / 899 27 179
julia.neugebauer@morphosys.com
Myles Clouston
Senior Director Investor Relations
Tel: +1 857-772-0240
myles.clouston@morphosys.com
SOURCE: MorphoSys AG
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