OncoResponse Announces Presentation of Preclinical Data on Dual Antibodies Targeting LILRB1 and LILRB2 at American Association for Cancer Research Annual Meeting 2023 (AACR 2023)

On March 15, 2023 OncoResponse, a clinical-stage biotech company advancing immunotherapies derived from the immune systems of Elite Cancer Responders, reported a poster presentation at the upcoming American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting being held April 14-19, 2023, at the Orange County Convention Center in Orlando, Florida (Press release, OncoResponse, MAR 15, 2023, View Source [SID1234628838]).

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Details are as follows:

Title: Discovery and preclinical characterization of dual antagonist antibodies targeting both LILRB1 and LILRB2 that enhance innate and adaptive anti-cancer immune responses

Abstract Presentation Number: 6376

Session Category/Title: Immunology/Immune Checkpoints

Location/Poster Board#: Section 23 / 20

Session Date and Time: Wednesday Apr 19, 2023, 9:00 AM – 12:30 PM

"We are pleased to provide our first presentation of preclinical data regarding our dual targeting antibodies for LILRB1 and LILRB2 at the upcoming AACR (Free AACR Whitepaper) conference," said Kamal Puri, PhD, Chief Scientific Officer of OncoResponse. "The presentation will detail both our discovery and preclinical characterization efforts."

Invitae to Present Data at The American Clinical Genetics Meeting 2023 That Supports Removing Barriers to Genetic Testing

On March 15, 2023 Invitae (NYSE: NVTA), a leading medical genetics company, reported seven studies, including one oral presentation and six posters, to be presented at the 2023 American Clinical Genetics Meeting held in Salt Lake City from March 14-18, 2023 (Press release, Invitae, MAR 15, 2023, View Source [SID1234628837]). The research reinforces the importance of universal genetic testing for patients with cancer, with much of the data highlighting the need for increased representation in clinical genetic testing data across racial, ethnic and ancestry groups that have long been underrepresented in genetic studies and databases. Such inclusion can uncover unique insights and expand the clinical validity of genetic testing to more populations, helping inform health journeys and potentially improving health outcomes. Invitae will also be highlighting powerful innovative technological advances that include multiplex assays of variant effects, machine learning and big data approaches to address current challenges in variant classification and promote reduction of variants of uncertain clinical significance (VUS).

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Key data being presented at ACMG 2023 include several studies that underscore the importance of removing barriers to germline genetic testing, whether that means expanding NCCN guidelines to go beyond familial risk-associated gene variants, increasing testing rates, or utilizing new innovations in variant classification to help reduce VUS across racial and ethnic groups.

Diversifying clinical studies to reveal impact across various race, ethnicity and ancestry identities

One such study, conducted in collaboration with researchers from University of California, Davis, highlights the inconsistencies between clinician entries and patients’ self-identified race, ethnicity and ancestry, particularly for non-White groups. The role of such inaccuracies for the implementation of precision medicine in minority groups is an area for further investigation. Another study compares and contrasts the rates of VUS in cancer predisposition genes in Black and White individuals. Although the rate of VUS-only results is higher in Black compared to White individuals, the number of unique VUS decreases at a higher rate in Black individuals over time.

"We look forward to presenting data at ACMG this year that is reflective of a more diverse patient population, and are committed to expanding these research efforts in the year ahead," said Robert Nussbaum, M.D., Invitae’s chief medical officer. "We’re continuing to explore race, ethnicity and ancestry implications to ensure clinical guidelines advance inclusivity and uncover clinically-actionable insights to support traditionally underrepresented groups."

Support for the expansion of clinical guidelines to support universal genetic testing for all patients

Several studies being presented at ACMG will highlight evidence around the benefits of genetic testing insights to advance testing as a standard of care for all patients. One particular study, conducted in collaboration with the City of Hope, analyzes the limitations of cascade testing for only the familial risk-associated gene variant, which is traditionally the course of action. Additionally, an oral presentation from David R. Wise, M.D., Ph.D., from New York University will explore how germline genetic testing has impacted clinical decisions for patients with prostate cancer, one of the most common cancers for American men.

"Each year, ACMG serves as a leading forum to present our findings to clinical geneticists who can change medical practice by making genetic testing part of the standard of care. We’re thrilled to share more data this year to advance precision medicine for all," said Dr. Nussbaum.

The following is a guide to Invitae-affiliated presentations at ACMG 2023.

2023 ACMG presentations:

Oral presentation: Titled: Real world impact of germline genetic testing on clinical decision making for prostate cancer patients. Presenter: David R. Wise, M.D., Ph.D. – Wednesday, March 15, 4:00–4:15 pm MST
Poster ID: P537: Titled: Reliability of clinician entries of patient self-identified race, ethnicity, and ancestry in clinical genetic testing. Presenter: Alice Popejoy Ph.D. – Thursday, March 16, 10:30 am–12:00 pm MST
Poster ID: P277: Titled: Modeling Cellular Evidence: Scalable Approaches for Generating, Validating and Incorporating Data from High-Throughput Functional Assays to Improve Clinical Variant Interpretation. Presented by Jason A. Reuter, Ph.D. – Thursday, March 16, 10:30 am–12:00 pm MST
Poster ID: P490: Titled: The impact of machine learning algorithms in reducing VUS for individuals from underrepresented populations compared to well studied populations. Presented by Britt Johnson, Ph.D., FACMG. – Friday, March 17, 10:30 am–12:00 pm MST
Poster ID: P088: Titled: What’s Trending: Comparing Variant of Uncertain Significance (VUS) Rates in Cancer Predisposition Genes Over Time in Black and White Individuals. Presented by Gail Tomlinson, M.D., Ph.D. – Friday, March 17, 10:30 am–12:00 pm MST
Poster ID: P058: Titled: Cascade testing with comprehensive multigene panels for hereditary cancer identifies unexpected findings in relatives. Presented by Brandie Heald, MS, CGC. – Friday, March 17, 10:30 am–12:00 pm MST
Poster ID: P244: Titled: Developing Probabilistic Graphical Models for Improved Variant Interpretation. Presented by Toby Manders, M.D. – Friday, March 17, 10:30 am–12:00 pm MST

Akeso Reported 2022 Annual Results

On March 15, 2023 Akeso Inc. (HKEX Code: 9926.HK, "Akeso", or the "Company") reported its 2022 annual report (Press release, Akeso Biopharma, MAR 15, 2023, View Source [SID1234628836]). During the reporting period, the company enjoyed booming business development and made breakthrough progress in drug innovation and development, commercialization and internationalization.

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开坦尼(cadonilimab, PD-1/CTLA-4 bispecific antibody)saw a strong start

With excellent safety and efficacy profile, a well-established commercialization platform and great efforts by the highly productive sales force, 开坦尼 recorded strong sales of RMB546.3 million for the financial year ended December 31, 2022.

On June 29, 2022, 开坦尼 , the first-in-class PD-1/CTLA-4 bi-specific antibody independently developed by the company, has been granted marketing approval by the NMPA for the treatment of recurrent or metastatic cervical cancer (R/M CC) patients who have progressed on or after platinum-based chemotherapy. 开坦尼 is the first approved dual immune checkpoint inhibitor bispecific antibody globally, addressing a huge unmet medical need for immunotherapy for advanced cervical cancer in China, and is also pioneering the development of bispecific antibodies in China.

安尼可(penpulimab injection, PD-1), jointly developed by Akeso and Sino Biopharmaceutical Limited (stock code: 1177.HK), recorded product sales of RMB558.1 million in 2022, increasing 164%. In April 2022, three indications were included in the 2022 CSCO Guideline, which are penpulimab for treatment of refractory/relapsed classic Hodgkin Lymphoma (r/r cHL), penpulimab in combination with chemotherapy as first-line treatment of squamous NSCLC, penpulimab as secondline treatment or salvage treatment of recurrent/metastatic nasopharyngeal carcinoma (r/m NPC). In January 2023, 安尼可 in combination with chemotherapy as first-line treatment of locally advanced or metastatic squamous non-small cell lung cancer was approved by NMPA.

Expediting global collaboration and development signified by landmark outlicensing transaction of ivonescimab (PD-1/VEGF, AK112)

Another breakthrough development was overseas licensing which set a new record for the transaction amount of a single innovative drug in China. In December 2022, exclusive development licensing rights were granted to Summit Therapeutics in the United States, Canada, Europe and Japan for ivonescimab, a breakthrough PD-1/VEGF bispecific antibody independently developed by Akeso. Akeso has received an upfront payment equivalent to US$500 million and the total potential deal value is up to US$5 billion, including regulatory and commercial milestone payments. Akeso will also receive a low double-digit percentage of royalties on net product sales.

Currently, the cooperation between the two sides has been deeply and completely carried out, which fully demonstrates the huge global commercialization potential of ivonescimab and paves a fast track for its globalization and commercialization.

Strong R&D efficiency contributed to six products in 14 Pivotal/Phase III studies

During the reporting period, Akeso’s new drug development entered the advanced stage in batches, and a total of 14 clinical studies were in the Pivotal/Phase III stage, six of which have completed enrollment and will soon submit marketing applications.

The Phase III clinical studies on 开坦尼 for major indications including first-line cervical cancer, first-line gastric cancer and hepatocellular cancer were advanced efficiently, while those for first-line cervical cancer and first-line gastric cancer were enrolled.

The patient enrollment of Phase III clinical trial of ivonescimab plus chemotherapy versus chemotherapy in EGFR mutated advanced non-squamous NSCLC that failed in prior EGFR-TKI therapy, has been completed. Ivonescimab monotherapy versus pembrolizumab monotherapy as the first-line treatment for NSCLC patients with positive PD-L1 expression is going well, and the Phase III trial of ivonescimab plus chemotherapy versus PD-1 inhibitor plus chemotherapy for advanced squamous NSCLC was approved. Ivonescimab has received Breakthrough Therapy Designation Status in China for three indications in lung cancer.

In the field of autoimmunity and metabolism, the first applications for new drug marketing are expected to be submitted in 2023 for two Phase III studies on ebdarokimab (IL-12/IL-23, AK101) for the treatment of moderate to severe psoriasis and ebronucimab (PCSK9, AK102) for the treatment of hypercholesterolemia.

"We are pleased to see our best performance since the company’s establishment, particularly the strong growth in sales of our two new drugs, as well as the record licensing agreements for our self-developed drug, which reflect the tremendous clinical and commercial value of our innovative drugs and demonstrate our robust commercialization capability in the first place. These achievements are mainly due to our strategic vision and R&D layout ability, its drug innovation R&D system at the forefront of science, a high standard and demanding production system, and our professional management and execution. These provide a solid foundation for us to fulfill our mission and embark on a new journey in biopharma," said Dr. Michelle Xia, co-founder, Chairwoman, CEO, and President of Akeso.

"Over the next five years, we will be launching more than six independently developed new drug varieties, covering a broad range of areas including cancer, autoimmunity and metabolism." Dr. Michelle Xia said.

MorphoSys AG Reports Fourth Quarter and Full Year 2022 Financial Results and Provides Corporate Update

On March 15, 2023 MorphoSys AG (FSE: MOR; NASDAQ: MOR) reported results for the fourth quarter and the full year 2022 (Press release, MorphoSys, MAR 15, 2023, View Source/en/news/morphosys-ag-reports-fourth-quarter-and-full-year-2022-financial-results-and-provides" target="_blank" title="View Source/en/news/morphosys-ag-reports-fourth-quarter-and-full-year-2022-financial-results-and-provides" rel="nofollow">View Source [SID1234628835]).

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"2022 was a defining year for MorphoSys. We made advances in our pipeline by progressing our Phase 3 clinical trials, including pelabresib in myelofibrosis and tafasitamab in lymphomas. We also out-licensed highly promising, early and mid-stage product candidates, enabling us to concentrate exclusively on our work in oncology," said Jean-Paul Kress, M.D., Chief Executive Officer of MorphoSys. "In 2023, we will continue to prioritize the Phase 3 study of pelabresib in myelofibrosis, on our way to sharing topline data in early 2024 and exploring its potential use in other myeloid diseases. We remain steadfast in our commitment to developing and delivering novel therapies that are safer and more effective for cancer patients, and we look forward to the future."

Pelabresib Highlights:

On January 9, 2023, MorphoSys announced that topline data from the ongoing Phase 3 MANIFEST-2 study are expected to be available in early 2024.

MorphoSys presented at ASH (Free ASH Whitepaper) 2022 results from analyses of the ongoing MANIFEST study in patients with myelofibrosis. The latest analyses include longer-term data showing durable improvements in both spleen volume and symptom score beyond 24 weeks, with pelabresib plus ruxolitinib in JAK inhibitor-naïve patients.

Monjuvi/Minjuvi Highlights:

Monjuvi (tafasitamab-cxix) U.S. net product sales of US$ 25.3 million (€ 24.7 million) for the fourth quarter 2022 (Q4 2021: US$ 23.6 million (€ 20.5 million)) and US$ 89.4 million (€ 84.9 million) for the full year of 2022 (2021: US$ 79.1 million (€ 66.9 million)).

Minjuvi royalty revenue of € 0.7 million for sales outside of the U.S. in the fourth quarter 2022 and € 3.0 million for the full year of 2022.

Tafasitamab Data:

At the ASH (Free ASH Whitepaper) conference in December 2022, final safety and efficacy results from firstMIND, a Phase 1b, open-label, randomized safety study combining tafasitamab or tafasitamab plus lenalidomide with standard R-CHOP were presented, showing no new safety signals and providing additional information on progression-free survival at 24 months for patients with newly diagnosed diffuse large B-cell lymphoma (DLBCL) treated with tafasitamab plus lenalidomide and R-CHOP. Two additional analyses also suggested that sensitive assays to detect minimal residual disease have prognostic value at the end of first-line therapy.

Corporate Developments:

On December 6, 2022, MorphoSys’ fully owned subsidiary Constellation Pharmaceuticals, Inc. entered into a global licensing agreement with Novartis to research, develop, and commercialize its preclinical inhibitors of a novel cancer target. Under the terms of the agreement, Novartis will assume full responsibility for all subsequent research, development, and commercialization activities for the program. As part of the agreement, MorphoSys received an immediate upfront payment of US$ 23 million. On achievement of development, regulatory, and commercial milestones, MorphoSys will be eligible to receive milestone payments from Novartis in addition to mid-single to low-double-digit royalties on program net sales.

On December 20, 2022, MorphoSys announced that Sung Lee, the company’s Chief Financial Officer and Management Board member, has decided to leave MorphoSys to move back to California. His last day with MorphoSys will be March 17, 2023.

Significant Events After the End of the Fourth Quarter of 2022:

On March 2, 2023, MorphoSys announced that it will stop work and operations on its pre-clinical research programs to optimize its cost structure. MorphoSys will reduce its workforce at the company’s headquarters in Planegg, Germany, by approximately 17%. This action, along with other steps taken over the past year, enables MorphoSys to focus resources on its mid- to late-stage oncology pipeline.

On March 14, 2023, MorphoSys announced that Lucinda Crabtree, Ph.D., will join as Chief Financial Officer and member of the Management Board. She will start in the third quarter 2023 at the latest.

Charlotte Lohmann was appointed as Chief Legal Officer on March 1, 2023 and will serve as a member of MorphoSys’ Management Board ad interim.

Financial Results for the Fourth Quarter of 2022 (IFRS):

Total revenues for the fourth quarter 2022 were € 81.6 million compared to € 52.9 million for the same period in 2021. This increase resulted mainly from higher revenues from the global licensing agreement with Novartis executed in the fourth quarter 2022.

in € million* Q4 2022 Q3 2022 Q4 2021 Q-Q Δ Y-Y Δ

Total revenues 81.6 95.8 52.9 (15) % 54 %
Monjuvi product sales 24.7 21.9 20.5 13 % 20 %
Royalties 29.1 29.7 23.2 (2) % 25 %
Licenses, milestones and other 27.9 44.1 9.3 (37) % > 100%
* Differences due to rounding.
Cost of Sales: In the fourth quarter of 2022, cost of sales was € 15.4 million compared to € 9.5 million for the same period in 2021. The fourth quarter of 2022 includes € 5.1 million of expenses related to activities to optimize the Monjuvi supply chain.

Research and Development (R&D) Expenses: In the fourth quarter 2022, R&D expenses were € 94.0 million compared to € 87.0 million for the same period in 2021. The increase is primarily due to clinical trial material expenses in the fourth quarter 2022 partially offset by lower personnel costs.

Selling, General and Administrative (SG&A) Expenses: Selling expenses in the fourth quarter 2022 were € 23.0 million compared to € 32.5 million for the same period in 2021. The decrease was driven by higher investments in 2021 made into the commercial organization, the first full year after the Monjuvi launch. General and administrative (G&A) expenses amounted to € 17.5 million compared to € 18.2 million for the same period in 2021.

Operating Loss: Operating loss amounted to € 68.4 million in the fourth quarter 2022 compared to a loss of € 325.0 million for the same period in 2021. The lower year-over-year operating loss was primarily driven by the impairment of goodwill amounting to € 230.7 million recognized in the fourth quarter 2021.

Consolidated Net Profit / Loss: For the fourth quarter 2022, consolidated net profit was € 329.4 million compared to a net loss of € 381.0 million for the same period in 2021. The consolidated net profit in the fourth quarter 2022 was driven mainly by the recognition of finance income triggered by the reduction in financial liabilities from collaborations.

Financial Results for the Full Year 2022 (IFRS):

Total Revenues for the full year 2022 were € 278.3 million compared to € 179.6 million in 2021. The increase resulted mainly from higher revenues from licenses due to the out-licensing agreements with HI-Bio and Novartis. Royalties in 2022 include € 3.0 million from the sale of Minjuvi outside of the U.S. by our partner Incyte and € 96.9 million from Tremfya sales which is fully passed on to Royalty Pharma.

in € million* 2022 2021 Y-Y Δ

Total revenues 278.3 179.6 55 %
Monjuvi product sales 84.9 66.9 27 %
Royalties 99.9 65.6 52 %
Licenses, milestones and other 93.5 47.2 98 %
* Differences due to rounding.
Cost of Sales: For the full year 2022, cost of sales were € 48.6 million compared to € 32.2 million in 2021. The increase was primarily driven by higher sales of Monjuvi in the U.S. and Minjuvi outside of the U.S. and expenses related to activities to optimize the Monjuvi supply chain.

R&D Expenses: For the full year 2022, R&D expenses were € 297.8 million compared to € 225.2 million in 2021. The R&D expenses increased primarily due to higher development activity and the inclusion of expenses from the Constellation acquisition since Q3 2021.

SG&A Expenses: Selling expenses for the full year 2022 were € 92.4 million compared to € 121.5 million in 2021. The decrease was primarily driven by higher investments made into the commercial organization in 2021, the first full year after the Monjuvi launch. G&A expenses amounted to € 60.1 million for 2022 compared to € 78.3 million in 2021. The decrease was driven primarily by the transaction costs related to the Constellation and Royalty Pharma agreements in 2021.

Operating Loss: Operating loss amounted to € 220.7 million for the full year 2022 compared to a loss of € 508.3 million in 2021. The lower year-over-year operating loss was primarily driven by the impairment of goodwill amounting to € 230.7 million recognized in 2021.

Consolidated Net Loss: For the full year 2022, consolidated net loss was € 151.1 million compared to a net loss of € 514.5 million in 2021. The lower consolidated net loss in 2022 was driven mainly by the recognition of finance income triggered by the reduction in financial liabilities from collaborations.

Cash and Other Financial Assets: As of December 31, 2022, the Company had cash and other financial assets of € 907.2 million compared to € 976.9 million on December 31, 2021.

Number of shares: The number of shares issued totaled 34,231,943 on December 31, 2022, no change compared to December 31, 2021.

Full Year 2023 Financial Guidance:

Amounts in million 2023 Financial Guidance 2023 Guidance Insights
Monjuvi U.S. net product sales US$ 80m to 95m 100% of Monjuvi U.S. net product sales are recorded on MorphoSys’ income statement and related profit/loss is split 50/50 between MorphoSys and Incyte.
Gross margin for Monjuvi U.S. net product sales 75% to 80% 100% of Monjuvi U.S. product cost of sales are recorded on MorphoSys’ income statement and related profit/loss is split 50/50 between MorphoSys and Incyte.
R&D expenses € 290m to 315m 2023 anticipated to be incrementally higher than 2022 due to the expansion of the pelabresib development program.
SG&A expenses € 140m to 155m 45% to 50% of mid-point of SG&A expenses represent Monjuvi U.S. selling costs of which 100% are recorded in MorphoSys’ income statement. Incyte reimburses MorphoSys for half of these selling expenses.
Additional information related to 2023 Financial Guidance:

Tremfya royalties will continue to be recorded as revenue without any cost of sales in MorphoSys’ income statement. These royalties, however, will not contribute any cash to MorphoSys, as 100% of the royalties will be passed on to Royalty Pharma.
MorphoSys anticipates receiving royalties for Minjuvi sales outside of the U.S.
MorphoSys does not anticipate any significant cash-accretive revenues from the achievement of milestones in 2023.
MorphoSys anticipates sales of commercial and clinical supply of tafasitamab outside of the U.S. to its partner Incyte. Revenue from this supply is recorded in the "Licenses, milestones and other" category in MorphoSys’ income statement. These sales result in a zero gross profit/margin. As such, MorphoSys does not provide guidance for these sales
Operational Outlook:

The following events and development activities planned for 2023 and beyond include the following:

full patient enrollment for the pivotal Phase 3 study (MANIFEST-2) of pelabresib in myelofibrosis (MF) in 2023 with topline results anticipated in early 2024;
primary analysis data from the Phase 3 study (inMIND) of tafasitamab in patients with indolent lymphoma (r/r FL/MZL) in 2024;
primary analysis data from the pivotal Phase 3 study (frontMIND) of tafasitamab in previously untreated DLBCL in the second half of 2025.
MorphoSys Group Key Figures (IFRS, end of financial year: December 31, 2022)

in € million Q4 2022 Q4 2021 Δ 2022 2021 Δ
Revenues 81.6 52.9 54 % 278.3 179.6 55 %
Product Sales 24.7 20.5 20 % 84.9 66.9 27 %
Royalties 29.1 23.2 25 % 99.9 65.6 52 %
Licenses, Milestones and Other 27.9 9.3 >100% 93.5 47.2 98 %
Cost of Sales (15.4) (9.5) 62 % (48.6) (32.2) 51 %
Gross Profit 66.2 43.4 53 % 229.6 147.4 56 %
Total Operating Expenses (134.6) (368.4) (63) % (450.4) (655.8) (31) %
Research and Development (94.0) (87.0) 8 % (297.8) (225.2) 32 %
Selling (23.0) (32.5) (29) % (92.4) (121.5) (24) %
General and Administrative (17.5) (18.2) (4) % (60.1) (78.3) (23) %
Impairment of Goodwill — (230.7) (100) % — (230.7) (100) %
Operating Profit / (Loss) (68.4) (325.0) (79) % (220.7) (508.3) (57) %
Other Income (7.8) 3.4 >(100)% 12.0 8.2 46 %
Other Expenses 7.4 (1.7) >(100)% (15.6) (6.4) >100%
Finance Income 325.0 (2.7) >(100)% 412.1 96.6 >100%
Finance Expenses 249.5 (89.0) >(100)% (165.9) (181.5) (9) %
Income from Reversals of Impairment Losses / (Impairment Losses) on Financial Assets 0.4 (0.2) >(100)% — 0.3 (100) %
Share of Loss of Associates accounted for using the Equity Method (4.0) — n/a (4.3) — n/a
Income Tax Benefit / (Expenses) (172.7) 34.4 >(100)% (168.6) 76.6 >(100)%
Consolidated Net Profit / (Loss) 329.4 (381.0) >(100)% (151.1) (514.5) (71) %
Earnings per Share, Basic and Diluted (in €) — (11.16) n/a (4.42) (15.40) (71) %
Earnings per Share, Basic 9.64 — n/a — — n/a
Earnings per Share, Diluted 8.93 — n/a — — n/a
Cash and other financial assets (end of period) 907.2 976.9 * (7) % 907.2 976.9 * (7) %

* Value as of December 31, 2021

MorphoSys will hold its conference call and webcast tomorrow, March 16, 2023, at 1:00pm CET (12:00pm GMT/8:00am EDT) to present the results for the fourth quarter and the full year 2022.

Participants for the conference call and webcast may pre-register and will receive dedicated dial-in details to easily and quickly access the call:

View Source;linkSecurityString=469447192

Please dial in 10 minutes before the beginning of the conference.

A live webcast and slides will be made available at the Investors section under "Events & Conferences" on MorphoSys’ website, View Source and after the call, a slide-synchronized audio replay of the conference will be available at the same location.

Consolidated Financial Statements 2022 (IFRS) are available for download at:

View Source/en/investors/financial-information

Medigene AG to report full year 2022 financial results on March 29, 2023

On March 15, 2023 Medigene AG (Medigene, FSE: MDG1, Prime Standard), an early-stage immuno-oncology platform company focusing on the discovery and development of T cell immunotherapies for solid tumors, reported its financial results and provide a corporate update for the fiscal year ended December 31, 2022 on Wednesday, March 29, 2023 (Press release, MediGene, MAR 15, 2023, View Source [SID1234628834]).

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Following the release of the full year 2022 financial results on Medigene’s website, the company will host a conference call that same day at 3 p.m. CET (9 a.m. ET).

Full details for the conference call and webcast are as follows:

Date March 29, 2023
Time 3:00 p.m. CET (9 a.m. ET)
U.S. Dial-in Number: +1 877-451-6152
Int’l Dial-in Number: +1 201-389-0879
Conference ID: 13736670
Webcast: Join the live webcast here or at View Source
Please dial in 10 minutes ahead of time to ensure a timely start of the conference call.

Following the call, an archived webcast will be accessible on the Investors & Media section of the Medigene website: View Source