Servier full year 2021/22 results confirm the
transformation trajectory of the Group

On February 2, 2023 Servier, an independent international pharmaceutical group, reported its financial results for the 2021/22 financial year and presents the main stages of its resolutely committed transformation (Press release, Servier, FEB 2, 2023, View Source [SID1234626809]).

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Extract from consolidated and audited results
(under IFRS [1] , ended September 30, 2022)

(in €m) 2021/22 2020/21 Variation Variation
at TCC [i]
Group turnover 4,876 4,441 +9.8% +6.6%
Turnover from the Princeps activity 3,694 3,282 +12.5% +8.9%
Revenue from the Generics business 1,182 1,159 +2.0% +0.0%
EBITDA 859 638 +34.6% –
EBITDA/turnover ratio 17.6% 14.4% +3.2pts –
Current operating income 442 251 +76% –
Net profit 192 (95) +287 –

"In a complex and unstable geopolitical and economic context, all of the Servier group’s business segments have progressed, confirming the trajectory of our transformation. I am proud of the work accomplished by our teams, which highlights our daily commitment to patients. Servier is now an international health player built around three balanced pillars: cardio-metabolism and venous diseases, oncology and generics. Our innovation capabilities have been strengthened and we now have a balanced and promising pipeline, in line with our ambition in oncology as well as in neurosciences and immuno-inflammation. The achievement of our 2025 objectives is on track and we are implementing our Servier 2030 strategic plan with determination and confidence."

Olivier Laureau, Chairman of Servier, declares
The Servier group’s consolidated revenue for the 2021/22 financial year increased by 9.8% compared to the 2020/21 financial year and reached 4.876 billion euros. This performance is notably driven by the growth in sales volume worldwide of 7.6% and a favorable exchange rate of 3.2% (+€140 million in fiscal year 2021/22 compared to a negative impact of
-€156 million the previous year). The complex context of pressure on prices had a negative effect on turnover growth of 1%, an impact of 45 million euros.

Sales of brand-name medicines amounted to €3.694 billion for the 2021/22 financial year, up 12.5% ​​compared to the 2020/21 financial year. Sales of generic drugs are up 2.0% compared to the previous financial year to reach 1.182 billion euros in 2021/22.

Top 3 of the strongest growth of the Group’s originator drugs in 2021/22

Medication 2021/22 revenue
(in €m) Progress
vs. 2020/21
(in €m at constant exchange rates i )
Tibsovo _ 256 +180
Daflon _ 552 +68
Triplixam _ 211 +37
EBITDA for the 2021/22 financial year amounted to 859 million euros, up 34.6%, and represents 17.6% of Group revenue compared to a ratio of 14.4% for the ‘Previous exercice. Current operating income for the 2021/22 financial year amounts to 442 million euros and corresponds to 9.1% of Group revenue. This performance is explained by the increase in international turnover, a favorable effect of exchange rates, coupled with very good control of expenses and the prioritization choices that were made during the financial year. . Net income, up, amounted to 192 million euros, or 3.9% of Group sales, compared to a loss of 95 million euros for the previous financial year.

"The results for the 2021/22 financial year confirm the Servier group’s trajectory and its ability to achieve its objectives of 6 billion euros in revenue and 1.3 billion euros in EBITDA in 2025. strong growth in sales in oncology as well as the major investments made in recent years confirm our strategy of becoming a focused and innovative player in oncology, projecting to achieve a turnover of 3 billion in this field in 2030. To enable the Group to invest in the long term, particularly in neurosciences and immuno-inflammation which constitute our growth drivers by 2030, our ambition is to increase the ratio of EBITDA to our turnover
to 30%. »

Pascal Lemaire, Executive Vice-President Finance of Servier
Strong growth in international sales
The share of turnover generated outside the European Union represents more than half of Group turnover, ie 56%, up 16% compared to the previous financial year. This strong growth can be explained in particular by the Group’s performance in the United States, which thus becomes the Group’s leading subsidiary, ahead of China, with revenue of 437 million euros compared to 255 million euros in 2020. /21. This 55% i growth is the result of the performance of the drug Tibsovo marketed by Servier in the United States since the second half of the 2020/21 financial year. In Japan, 2ndworld market in oncology, the subsidiary Nihon Servier achieved a turnover of 97 million euros in 2021/22 thanks to the sales of Onivyde , the marketing of which was initiated in June 2020.

The originator sales in France represent 2.7% of the Group’s sales, when this territory concentrates 51% of the Group’s investments, in particular industrial and R&D, for this financial year; a figure that testifies to Servier’s continued desire to create value in France for all of its stakeholders.

Confirmed 2025 objectives and a new ambition for 2030
The 2021/22 annual results confirm the Group’s trajectory for 2025 and its ability to achieve its objectives: revenue of 6 billion euros, including 1 billion euros in oncology, and EBITDA of 1.3 billion euros. euros, i.e. approximately 20% of turnover in 2025.

Achieving the 2025 objectives is a key step for the Group in order to tackle the second stage of its transformation plan for 2030, which is based on three pillars:

Be a focused and innovative mid-size player in oncology, as well as in neurosciences and immuno-inflammation
Maintain the Group’s leadership in cardio-metabolism and in venous diseases
Pursue the profitable growth of the generics business
The Group wishes to accelerate its transformation dynamic in order to guarantee, over the long term, its independence and its creation of value, and to generate a significant societal impact to contribute to a sustainable world. Thus, Servier plans to achieve a turnover of 8 billion euros in 2030 with an EBITDA ratio above 30%.

Cardio-metabolism and venous diseases, consolidated leadership
Sales of originator drugs in cardio-metabolism and venous diseases (CMVD) amounted to 2.693 billion euros and now represent 55.2% of the Group’s consolidated sales.

The growth of 2.9% i compared to the 2020/21 financial year is notably attributable to the performance of Daflon . Marketed in more than 100 countries, Daflon is the Group’s leading drug with sales of 552 million euros. Servier has invested since 2021, more than 100 million euros on its Oril Industrie site in Normandy (France) in order to adapt the production of the active ingredient of Daflon and to meet growing international demand.

Servier also intends to assert its leadership in the field of cardio-metabolism – the Group is the world’s 3rd largest pharmaceutical player in cardiology and the 2nd in hypertension [ 2] – by relying on its expertise in incremental innovation (Single Pill Combinations) and digital services to improve diagnosis, knowledge of chronic diseases and treatment compliance. Triplixam thus reached a turnover of 211 million euros in 2021/22.

Servier involves patients and patient associations in all projects in order to optimize the effectiveness of the solutions proposed to improve therapeutic adherence. In this regard and in the field of hypertension, Servier works in particular with Global Heart Hub and Senior International Health Association. This collaboration resulted in initial study results, presented at the European Society of Hypertension (ESH) 2022 Congress . The Group thus aims to improve adherence to treatment for patients suffering from this chronic disease and thus their life expectancy by avoiding comorbidities.

Oncology, the realization of an ambitious strategy in 2021/22
The share of oncology in consolidated sales rose sharply compared to the previous year to reach 848 million euros (up 35.4% i ), representing 17.4% of sales. consolidated business, compared to 13.6% in 2020/21. This performance is notably driven by sales of Tibsovo for 256 million euros in 2021/22. Tibsovo joined Servier’s portfolio in mid-2020/21, following the acquisition of the oncology division of Agios Pharmaceuticals. In 2022, Servier submitted a marketing authorization application to the European Medicines Agency (EMA) for Tibsovo .

Sales of other oncology drugs also contributed to this performance, including Oncaspar , with sales of 290 million euros, up 2.8% i , and Onivyde which achieved sales of 145 million euros in 2021/22, up 13.7% i compared to the previous financial year.

All of these indicators support the Group’s growth strategy in oncology. With nearly 6 billion in investments made over the past five years, Servier now has a portfolio of 7 drugs available to patients targeting pathologies with a strong unmet medical need.

The Group devotes more than 50% of its R&D budget to oncology, with the ambition of being recognized as a focused and innovative player in the development of treatments targeting hard-to-treat cancers. Servier directs its R&D programs in oncology around two approaches: immuno-oncology and targeted therapies. In addition, this major investment by the Group is now reflected in a promising pipeline of 38 R&D projects in oncology (as of January 2023).

A balanced and innovative pipeline, reflecting the successful transformation of R&D
With 43 projects in clinical development and 32 research projects [3] , the result of significant and continuous investment in R&D (more than 20% of originator sales), Servier focuses its research and development efforts on all of its therapeutic areas where the needs are major. To date, 50% of the Group’s Research projects have the potential to become "first in class" (drug with a new and unique mechanism of action) and the quality of its projects should lead the Group to launch two to three first in human studies per year.

With 21 projects in neurosciences and immuno-inflammation, Servier has built a quality pipeline capable of constituting its next source of growth.

"The quality of our pipeline concretely attests to the transformation of our R&D in our three therapeutic areas. This year, we demonstrated our ability to accelerate the process of discovering and making innovative therapies available to patients, through strategic partnerships and increased use of digital technologies. »

Claude Bertrand, Executive Vice-President Research & Development of Servier
Thus, during the 2021/22 financial year, Servier entered into new partnerships and reached important milestones regarding studies carried out in collaboration with partners. The Group notably entered into a collaborative research agreement with Oncodesign Precision Medicine (OPM) for the identification of new targets in pancreatic cancer. Also with this partner, an exclusive worldwide license option was exercised for a drug candidate in the treatment of Parkinson’s disease. Finally, in Sjögren’s Syndrome, this year marked the end of the inclusion of patients in a phase 2a clinical study conducted by Servier in partnership with OSE Immunotherapeutics, the results of which are expected in 2023.

In order to accelerate the development and marketing of new drugs and services, the Group has also entered into a strategic collaboration with Google Cloud, centered on the use of data. Servier has also entered into a partnership with GNS in the digital twin aimed at accelerating the discovery and clinical development of new treatments through AI and biosimulation.

The opening of the Servier Research and Development Institute in Paris-Saclay, during the
1 sthalf of 2023, constitutes a major step in the transformation of R&D. The result of an investment of nearly 400 million euros, it illustrates Servier’s ambition to build open, dynamic, productive and innovative research for the benefit of patients. It will be the heart of the Group’s global R&D organization and will work cross-functionally with the other R&D centers located in Budapest in Hungary, Ballerup in Denmark and Boston in the United States, as well as with the 3 hubs ( Europe, Asia-Pacific, America) for clinical research. Servier has also joined forces with BioLabs, a leading American player in the management and management of start-up incubators, for the management of its "Spartners" incubator in Paris-Saclay. The latter will host young shoots in the field of health and life sciences.

During the summer of 2022, Servier inaugurated its first Research center in Boston. Located at the heart of the world’s largest health ecosystem, the center brings together nearly 200 employees who work every day to develop innovative cancer treatments.

Generics, a strategy of local champions confirmed
Over the 2021/22 financial year, revenue from the Servier group’s generics activity remained stable compared to the previous financial year at constant exchange rates and amounted to 1.182 billion euros (24.2% of consolidated turnover of the Group). The favorable impact of sales volume growth on sales was neutralized by very strong pressure on net prices, particularly at Biogaran, and a very significant increase in the safeguard clause in France.

Today, the Group has an offer of more than 1,500 generic drugs covering the majority of pathologies and which are distributed throughout the world by four subsidiaries: EGIS in Eastern Europe, Pharlab in Brazil, Swipha in Nigeria and Biogaran, leader in the generics market in France.

Biogaran has thus consolidated its leadership around its range of reimbursed drugs, reaching 32% market share for generic drugs and has begun to diversify its activity with the ambition of becoming the reference player in the daily health of French people in the pharmacy. Biogaran, for example, launched a new range of technical dressings for wound care, developed its OTC offer, and the company also marketed GSK’s flu vaccine. It also intends to capitalize on the opening of the right to substitute biosimilar drugs in pharmacies to develop its presence in this fast-growing market.

Patient and CSR commitments at the heart of the Group’s strategy
Servier is committed to therapeutic progress for the benefit of patients. The Group thus works with patients at each stage of the drug’s life cycle. This reality was rewarded in June 2022 by a notable progression in the rankings resulting from the survey carried out by the organization PatientView in 2021 among patient associations around the world. Servier is notably ranked 7th out of 30 oncology laboratories.

During the year, Servier also acted to reduce its environmental footprint and contribute to the fight against climate change. The Group’s efforts have focused on all aspects of its business and have included in particular the eco-design of drugs, the decarbonization of its supply chain and the preservation of biodiversity. Beyond the Group’s desire to reduce its CO 2 emissions by 25% by 2030 (vs. 2015/16), more than 30,000 tonnes of CO 2 equivalent have been offset by Servier in 2022 thanks to projects capturing or limiting emissions.

A milestone in terms of diversity and inclusion, the Group launched "She is Servier", a female leadership program aimed at supporting and accompanying the women of the Group in their professional development. By 2024, Servier intends to reach a target of at least 40% women in top management.

Finally, and as part of its 2030 ambition, Servier plans to commit to a flagship CSR project every three years, in line with the Group’s vocation.

Repare Therapeutics to Participate in Two Upcoming Investor Conferences

On February 2, 2023 Repare Therapeutics Inc. ("Repare" or the "Company") (Nasdaq: RPTX), a leading clinical-stage precision oncology company, reported that members of its senior management team will participate at two investor conferences in February and March. Details for the fireside chats are as follows (Press release, Repare Therapeutics, FEB 2, 2023, View Source [SID1234626808]).

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Guggenheim Oncology Conference
Date: Thursday, February 9, 2023
Time: 3:20 p.m. Eastern Time
Location: New York, NY

Cowen 43rd Annual Health Care Conference
Date: Wednesday, March 8, 2023
Time: 9:50 a.m. Eastern Time
Location: Boston, MA

A live webcast of the fireside chats can be accessed in the Investor section of the Company’s website at View Source A replay of the webcasts will be archived on the Company’s website for at least 30 days.

Takeda Reinforces Long-term Growth Through Pipeline Advancement and Two Targeted Acquisitions; Delivers Another Strong Quarter in FY2022 Q3

On February 2, 2023 Takeda (TOKYO:4502/NYSE:TAK) reported financial results for the third quarter of fiscal year 2022 (period ended December 31, 2022) (Press release, Takeda, FEB 2, 2023, View Source [SID1234626807]).

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Takeda chief financial officer, Costa Saroukos, commented:
"Our third-quarter performance demonstrates sustained momentum as our Growth and Launch Products and solid commercial execution again drove strong revenue and core profit growth. We continue to advance our organic pipeline, including notable approvals in the EU and China, and in December announced a significant acquisition that will add a potentially best-in-class TYK2 inhibitor to our late-stage pipeline and enhance our long-term growth strategy. Our robust cash flow and strong financial position enabled us to make substantive progress in deleveraging even as we continued to invest for growth."

FINANCIAL HIGHLIGHTS

Results for FY2022 Q3 Ended December 31, 2022

(Billion yen,
except
percentages and
per share
amounts)

REPORTED

CORE(c)

(Non-IFRS)(a)

FY2022 Q3 YTD

vs. PRIOR YEAR

(Actual % change)

FY2022 Q3 YTD

vs. PRIOR YEAR

(Actual % change)

vs. PRIOR YEAR

(CER % change(d))

Revenue

3,071.3

+13.9%

3,071.3

+19.8%

+4.5%

Operating Profit

401.9

-13.1%

954.7

+26.0%

+9.7%

Margin

13.1%

-4.1pp

31.1%

+1.5pp

Net Profit

285.9

+18.4%

707.2

+35.6%

+15.9%

EPS (yen)

184

+19.6%

456

+37.0%

+17.1%

Operating Cash Flow

683.5

-8.6%

Free Cash Flow

(Non-IFRS)(a)(b)

585.2

-12.8%

(a) Further information regarding certain of Takeda’s Non-IFRS measures is posted on Takeda’s investor relations website at View Source

(b) We define Free Cash Flow as cash flows from operating activities, subtracting acquisition of property, plant and equipment ("PP&E"), intangible assets and investments as well as removing any other cash that is not available to Takeda’s immediate or general business use, and adding proceeds from sales of PP&E, as well as from sales of investments and businesses, net of cash and cash equivalents divested.

(c) Core results adjust our reported results calculated and presented pursuant to IFRS to exclude the effect of items unrelated to Takeda’s core operations, such as, to the extent applicable for each line item, non-recurring items, purchase accounting effects and transaction related costs, as well as amortization and impairment of intangible assets and other operating income and expenses.

(d) CER (Constant Exchange Rate) change eliminates the effect of foreign exchange rates from year-over-year comparisons by translating Reported or Core results for the current period using corresponding exchange rates in the same period of the previous fiscal year.

COMMERCIAL UPDATES ACROSS FIVE KEY BUSINESS AREAS
Growth in our key business areas in FY2022 Q3 YTD was driven largely by Growth & Launch Products1, which delivered reported revenue of 1,199.6 billion yen, marking a +20% increase on a CER basis.

Gastroenterology (GI), with 857.5 billion yen in reported revenue, grew +11% on a CER basis, driven by ENTYVIO (for ulcerative colitis and Crohn’s disease; +17% on a CER basis) and by TAKECAB/VOCINTI (for acid-related diseases), whose strong uptake in China was also a key contributor to growth.
Rare Diseases, with 553.6 billion yen in reported revenue, grew +5% on a CER basis. Sales of TAKHZYRO (for hereditary angioedema) grew +25% on a CER basis due to expansion of the prophylactic market, continued geographic expansion and strong patient uptake. LIVTENCITY (for post-transplant cytomegalovirus) continues to generate high interest and strong uptake since its launch in the U.S. in December 2021, with 87% of U.S. transplant centers having initiated therapy with at least one patient.
Plasma-Derived Therapies (PDT) Immunology, with 502.4 billion yen in reported revenue, delivered outstanding growth of +18% on a CER basis. Growth was driven by higher sales of immunoglobulin products (for primary immunodeficiency and multifocal motor neuropathy), with +19% growth on a CER basis, particularly in the U.S. amid easing of pandemic pressures coupled with increasing supply. Robust growth for albumin products (primarily used for hypovolemia and hypoalbuminemia), at +20% on a CER basis, was driven by strong demand in the U.S. and in China. We added 5 donation centers as planned in the U.S. in FY2022 Q3, bringing us to 21 new centers YTD, and our global donation network to 225 centers.
Oncology, with 345.0 billion yen in reported revenue, declined -13% on a CER basis as a result of the expected entry of VELCADE generics (for multiple myeloma) that began in the U.S. in May 2022. Besides VELCADE, all other revenue totaled 320.2 billion yen, a year-over-year increase of +7% on a CER basis, driven by strong demand for ALUNBRIG (for non-small cell lung cancer; +39% growth on a CER basis) in Europe and Growth & Emerging Markets, and China. ADCETRIS (for malignant lymphomas) grew +18% on a CER basis, driven by increased access and uptake in frontline indications, while increased awareness of positive OPTIC trial results and label update contributed to +13% growth of ICLUSIG (for Leukemia) on a CER basis. Sales of EXKIVITY (for non-small cell lung cancer), which was first launched in the U.S. in September 2021 followed by several other countries, also contributed.
Neuroscience, with 477.1 billion yen in reported revenue, grew +10% on a CER basis, driven by an expanding ADHD adult market in the U.S., Europe and Canada for VYVANSE/ELVANSE. Sales of TRINTELLIX were 79.7 billion yen (+5% growth on a CER basis), due to continued recovery of the Major Depressive Disorder market in the U.S. and strong market share gains in Japan.
PIPELINE UPDATE
Takeda has continued to deliver on its ability to bring new therapies to patients and capitalize on momentum within its innovative pipeline. Updates since the FY2022 H1 announcement include:

Takeda announced that it has entered into an exclusive licensing agreement with HUTCHMED for the further development and commercialization of fruquintinib worldwide (ex-China, Hong Kong, and Macau). Fruquintinib is a highly selective inhibitor of vascular endothelial growth factor receptors (VEGFR) -1, 2 and 3. It is orally administered and offers a potential new treatment option for patients with refractory metastatic colorectal cancer, regardless of biomarker status.
Additional information related to this announcement is available here.
Takeda announced that it will acquire NDI-034858, an oral selective allosteric TYK2 inhibitor being evaluated for the potential treatment of multiple autoimmune diseases, from Nimbus Therapeutics. With Phase 3 studies in psoriasis expected to begin this year, NDI-034858 has the potential to demonstrate best-in-class efficacy and safety and convenience in psoriasis as well as other immune-mediated diseases including psoriatic arthritis, inflammatory bowel disease and systemic lupus erythematosus. The acquisition is expected to strengthen Takeda’s growing late-stage pipeline in alignment with the company’s therapeutic area strategy and expertise in immune-mediated diseases. Takeda will pay Nimbus USD 4 billion upfront in addition to two milestone payments of USD 1 billion each upon achieving annual net sales of USD 4 billion and USD 5 billion for products developed from the NDI-034858 program. The upfront payment will be primarily funded by cash on hand. The transaction is expected to be finalized before the end of FY2022.
Additional information related to this announcement is available here.
QDENGA, Takeda’s dengue vaccine, was approved by the European Commission (EC) in December 2022 for use in individuals four years of age and older. With the EC approval, QDENGA becomes the only dengue vaccine approved in the EU for use in individuals regardless of previous dengue exposure. In November, the U.S. FDA granted priority review of the Biologics License Application.
Additional information related to the EC and U.S. FDA announcements is available here and here.
China’s National Medical Products Administration (NMPA) approved EXKIVITY (mobocertinib) for the treatment of adult patients with locally advanced or metastatic non-small cell lung cancer with epidermal growth factor receptor Exon20 insertion mutations, whose disease has progressed on or after platinum-based chemotherapy. EXKIVITY is now the first and only treatment available for this patient population in China and was reviewed as part of the NMPA’s Breakthrough Therapy program.
Additional information related to this announcement is available here.
LIVTENCITY (maribavir) was approved by the European Commission (EC) for the treatment of adults with post-transplant cytomegalovirus (CMV) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies. This approval makes LIVTENCITY the first and only treatment approved for this indication by the EC. CMV is one of the most common and serious post-transplant infections and can lead to loss of transplanted organ and failure of graft.
Additional information related to this announcement is available here.
Takeda announced favorable safety and efficacy results of TAK-755 from the first and only Phase 3 trial in congenital thrombotic thrombocytopenic purpura (cTTP), an ultra-rare disease with limited treatment options. Based on this data, Takeda aims to seek marketing authorization for TAK-755 as the first recombinant ADAMTS13 replacement therapy for cTTP, a disorder with considerable unmet patient need.
Additional information related to this announcement is available here.
Takeda and Arrowhead Pharmaceuticals Inc. announced topline results from the SEQUOIA Phase 2 study of investigational fazirsiran (TAK-999/ARO-AAT) in patients with liver disease associated with alpha-1 antitrypsin deficiency (AATD-LD). Takeda has initiated a Phase 3 study to evaluate the safety and efficacy of fazirsiran in the treatment of patients with AATD-LD with METAVIR stage F2 to F4 fibrosis.
Additional information related to this announcement is available here.
Results from Takeda’s Phase 3 AURORA trial provided evidence of maribavir’s clinically meaningful and durable effect in cytomegalovirus infection in hematopoietic stem cell transplant patients despite missing the primary endpoint. Full data results will be submitted for publication in a peer-reviewed journal and are being shared with relevant regulatory agencies.
Additional information related to this announcement is available here.
Takeda’s Phase 3 PhALLCON trial met its primary endpoint, demonstrating that adult patients with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) treated with ICLUSIG (ponatinib) plus reduced-intensity chemotherapy achieved higher rates of minimal residual disease-negative complete remission compared to imatinib. There are currently no targeted treatments approved for Ph+ ALL in the U.S.
Additional information related to this announcement is available here.
TAK-861, Takeda’s oral orexin agonist for narcolepsy, met pre-specified criteria set to advance the program into two Phase 2b studies in narcolepsy type 1 and narcolepsy type 2. Both Phase 2b trials are currently enrolling patients.
Additional information related to this update is available here.
FY2022 Outlook

On track towards full-year FY2022 Management Guidance

(Billion yen)

FY2022
FORECAST
(Upgraded
October 2022)

FY2022
MANAGEMENT GUIDANCE
Core Growth at CER
(Non-IFRS)
(Unchanged from May 2022)

Revenue

3,930.0

Core Revenue

3,930.0

Low-single-digit growth

Reported Operating Profit

530.0

Core Operating Profit

1,180.0

High-single-digit growth

Reported Net Profit

307.0

Reported EPS (Yen)

198

Core EPS (Yen)

525

High-single-digit growth

Free Cash Flow

650.0 – 750.0

Annual Dividend per Share (Yen)

180

Free Cash Flow forecast does not include the impact of the upfront cash payment for the acquisition of NDI-034858 from Nimbus Therapeutics, LLC for USD 4 billion, as the exact timing of cash payment is dependent upon deal close.

For more details on Takeda’s FY2022 Q3 results and other financial information including key assumptions in FY2022 forecast and management guidance, please visit: View Source

ADC Therapeutics Announces Pricing of Underwritten Offering by a Selling Shareholder

On February 2, 2023 ADC Therapeutics SA ("ADCT" or the "Company") (NYSE: ADCT), a commercial-stage biotechnology company helping to improve the lives of those affected by cancer with its next-generation, targeted antibody drug conjugates, reported the pricing of an underwritten offering of 12,000,000 common shares of the Company currently owned by A.T. Holdings II Sàrl (the "Selling Shareholder"), an affiliate of Auven Therapeutics Holdings L.P., at a price of $5.00 per share (before underwriting discounts and commissions) (Press release, ADC Therapeutics, FEB 2, 2023, View Source [SID1234626806]). ADCT is not selling any common shares and will not receive any proceeds from the sale of the common shares in the offering. The offering is expected to close on February 6, 2023, subject to customary closing conditions.

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The offering included participation from Redmile Group, Perceptive Advisors, Frazier Life Sciences and Surveyor Capital (a Citadel company) along with other institutional investors.

Jefferies is acting as sole book-running manager for the offering.

The offering is being made pursuant to an effective registration statement (including a prospectus) on Form F-3 previously filed with the Securities and Exchange Commission ("SEC"). A final prospectus supplement and accompanying prospectus relating to the offering will be filed with the SEC and will be available on the SEC’s website located at www.sec.gov. Copies of the final prospectus supplement and accompanying prospectus relating to this offering, when available, may be obtained from Jefferies LLC, Attention: Equity Syndicate Prospectus Department, 520 Madison Avenue, New York, NY 10022, telephone: (877) 821-7388, email: [email protected].

This press release shall not constitute an offer to sell or a solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification of these securities under the securities laws of any such state or other jurisdiction.

Flare Therapeutics to Present at Guggenheim Healthcare Talks 2023 Oncology Day

On February 2, 2023 Flare Therapeutics, a biotechnology company targeting transcription factors to discover precision medicines for cancer and other diseases, reported that management will present a company overview at the upcoming Guggenheim Healthcare Talks 2023 Oncology Day on Thursday, February 9, 2023 at 2:45 p.m. ET in New York, NY (Press release, Flare Therapeutics, FEB 2, 2023, View Source [SID1234626805]).

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