Chugai Announces 2022 Full Year Results and Forecasts for 2023

On February 2, 2023 Chugai Pharmaceutical Co., Ltd. (TOKYO: 4519) reported its consolidated financial results for the fiscal year ended December 31, 2022, and forecasts for the fiscal year ending December 31, 2023 (Press release, Chugai, FEB 2, 2023, View Source [SID1234626762]).

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"In 2022, the second year of Chugai’s growth strategy TOP I 2030, Chugai’s revenue exceed ¥1 trillion for the first time, and we achieved record-high revenues and profits for the sixth consecutive year. Domestic sales were driven by steady market penetration of our new products, including Vabysmo, which is our first full-scale entry into the ophthalmology field. In addition, the supply of Ronapreve (an antibody cocktail for COVID-19) to the government also contributed. The mainstay product Hemlibra continued to drive growth in overseas sales. In R&D, the new drug discovery research center ‘Chugai Life Science Park Yokohama’ was completed in October, which will serve as the foundation to maximize our drug discovery capabilities. In addition, clinical studies have begun for several in-house projects applying Chugai’s proprietary antibody engineering technologies, which will further enhance our pipeline for medium to long-term growth. In 2023 we will enter a new phase in our financial performance, as we move away from the initial contribution of COVID-19-related drugs. However, excluding the temporary impact of those products, we expect revenue growth this fiscal year as our core business in Japan and overseas is solid, with a robust portfolio of products and projects that will support our future growth. ‘Chugai Life Science Park Yokohama’ will go into full-scale operation this April. From this new drug discovery research center, we will continue to pursue innovation in order to deliver innovative new drugs to patients as quickly as possible," said Dr. Osamu Okuda, Chugai’s President and CEO.

Chugai reported financial results for 2022 with revenues of ¥1,168.0 billion (+¥168.2 billion, +16.8), royalties and other operating income declined by approximately 30%, while sales increased by approximately 30%. Sales exceeded ¥1 trillion for the first time since Chugai’s foundation, with record-high revenue and core operating profit for the sixth consecutive year.

Domestic sales were ¥654.7 billion (+¥135.8 billion, +26.2%). Sales in the oncology field decreased by approximately 2% as the impact of the NHI drug price revision and biosimilars in mature products, including Avastin and Herceptin, exceeded the sales growth from a new product Polivy, and a mainstay product Kadcyla as well as Foundation Medicine business. Sales in the specialty field increased by more than 50% due to the significant increase in sales from the supply of Ronapreve to the government, as well as an approximately 20% increase in sales of the mainstay product Hemlibra, and the contributions from the steady market penetration of new products, including Evrysdi, Enspryng and Vabysmo. Overseas sales were ¥384.6 billion (+¥100.7 billion, +35.5%). Hemlibra increased significantly by approximately 70% owing to the full-scale export to Roche at regular shipping price, and Actemra also showed solid growth. Royalties and other operating income decreased by approximately 30%, mainly due to a significant decrease in royalty income related to the initial shipments of Hemlibra.

The cost to sales ratio rose by 3.9% points year-on-year to 45.7%, mainly due to changes in the product mix. Operating expenses grew by approximately 5% as marketing and distribution expenses slightly increased and research and development expenses increased, while general and administration expenses decreased. Marketing and distribution expenses slightly increased mainly due to the impact of foreign exchange. Research and development expenses increased mainly due to the progress of development projects under development and the effects of foreign exchange. General and administration expenses decreased mainly due to decreases in various expenses and recognizing gains on sales of property, plant and equipment. As a result, Core operating profit totaled ¥451.7 billion (+¥17.6 billion, +4.1%).

Reflecting the favorable results and based on our dividend policy, Chugai plans to pay year-end dividends of ¥40 per share. As a result, the annual dividend will be ¥78 per share, and the Core dividend payout ratio is 42.0% on a five-year average basis (40.4% on a single fiscal year basis).

Regarding research and development, the Company made good progress in both early and late-stage development toward achieving TOP I 2030. For in-house projects, applying Chugai’s proprietary antibody engineering technologies, DONQ52, RAY121, and ALPS12 entered the clinical development stage for celiac disease, autoimmune disease, and solid tumors, respectively. For crovalimab, the world’s first application for approval for the treatment of paroxysmal nocturnal hemoglobinuria (PNH), was filed in China and granted priority review designation. Also, Roche initiated overseas development for sickle cell disease. Simultaneous development for in-house products is also in progress, with new clinical studies initiated for Enspryng in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and autoimmune encephalitis (AIE), and GYM329 in spinal muscular atrophy (SMA), in combination with Evrysdi. Furthermore, Maruho, the licensee of nemolizumab (product name: Mitchga) in Japan, obtained approval and launched the new product in August to treat itching associated with atopic dermatitis. For NXT007, which is being developed as the next-generation project following Hemlibra, Chugai and Roche entered a license agreement. Among products in-licensed from Roche, Tecentriq and Polivy received approval for additional indications for adjuvant treatment of non-small cell lung cancer and previously untreated diffuse large B-cell lymphoma, respectively. Several new projects mainly in the oncology area, were added to the Company’s pipeline. In addition, the company has entered into a license agreement with Noile-Immune Biotech for its PRIME CAR-T Technology, progressing steadily to achieve its multi-modality strategy.

In 2023, Core revenues, Core operating profit, and Core net income are expected to be ¥1,070.0 billion (-¥97.8 billion, -8.4%), ¥415.0 billion (-¥36.7 billion, -8.1%), and ¥306.0 billion (-¥11.7 billion, -3.7%), all of which will be lower than those in the previous year respectively. Sales are expected to decrease both in Japan and overseas, totaling ¥920.0 billion (-¥119.2 billion, -11.5%). Domestic sales are expected to decrease due to the reduction in the supply of Ronapreve to the government and the effect of generics, while new products and mainstay products will grow in both oncology and specialty fields. The supply of Ronapreve to the government is expected to be ¥81.2 billion, and the domestic sales excluding Ronapreve are expected to increase steadily to ¥460.5 billion (+¥9.5 billion, +2.1%). Overseas sales are expected to decrease slightly to ¥378.3 billion (-¥6.3 billion, -1.6%) due to sales declines of Hemlibra and Actemra, while Alecensa will grow. Sales of Hemlibra are expected to decrease due to the effect of the optimization of inventory levels at Roche and the effects of lower export price. Actemra is expected to decrease mainly due to a decline in COVID-19 demand. Other revenue* is expected to increase to ¥150.0 billion (+¥21.4 billion, +16.6%), driven by an increase in royalty and profit-sharing income from Hemlibra and one-time income.

*The category "Royalties and other operating income" until the fiscal year ended December 31, 2022, has been renamed. In addition, income from disposal of product rights is excluded from this category.

For the fiscal year 2023, Chugai expects annual dividends per share of ¥80 with a Core dividend payout ratio of 41.8% on a five-year average basis (43.0% on a single fiscal year basis).

[2022 full year results]

Billion JPY 2022 2021 % Change
Core results
 Revenues 1,168.0 999.8 +16.8%
  Sales 1,039.2 802.8 +29.4%
  Royalties and other operating income 128.8 196.9 △34.6%
 Operating profit 451.7 434.1 +4.1%
 Net income 317.7 311.5 +2.0%
IFRS results*
 Revenues 1,259.9 999.8 +26.0%
 Operating profit 533.3 421.9 +26.4%
 Net income 374.4 303.0 +23.6%
*IFRS results include non-Core items, such as the income and other related items, which totaled ¥90.7 billion associated with the settlement agreement between Chugai and Alexion Pharmaceuticals, Inc., which are excluded from the Core results Chugai adopts to manage recurring business activities.

[2023 full year forecast]

Billion JPY 2023 Forecast 2022 Actual* % Change
Core-basis
 Revenues 1,070.0 1,167.8 △8.4%
 Operating profit 415.0 451.7 △8.1%
 Net income 306.0 317.7 △3.7%
*The amounts shown are after the reclassification of actual results following a partial change in the method of presentation starting in 2023.

[Progress in R&D activities for Oct 25th, 2022-Feb 2nd, 2023]

2022 Q4 R&D Progress

About Core results

Chugai discloses its results on a Core basis from 2013 in conjunction with its decision to apply IFRS. Core results are the results after adjusting non-Core items to IFRS results. Chugai’s recognition of non-recurring items may differ from that of Roche due to the difference in the scale of operations, the scope of business and other factors. Core results are used by Chugai as an internal performance indicator, for explaining the underlying business performance both internally and externally, and as the basis for payment-by-results such as a return to shareholders.

Trademarks used or mentioned in this release are protected by law.

Cardinal Health Reports Second Quarter Fiscal Year 2023 Results and Raises Fiscal Year 2023 Non-GAAP EPS Guidance

On February 2, 2023 Cardinal Health (NYSE: CAH) treported second quarter fiscal year 2023 revenues of $51.5 billion, an increase of 13% from the second quarter of fiscal year 2022 (Press release, Cardinal Health, FEB 2, 2023, View Source [SID1234626761]). Second quarter GAAP operating loss was $119 million due to a non-cash, pre-tax goodwill impairment of $709 million related to the Medical segment. GAAP diluted loss per share was $0.50, primarily due to this impairment, net of tax effects. Second quarter non-GAAP operating earnings of $467 million were in-line with the second quarter of last year. Non-GAAP diluted earnings per share (EPS) increased 4% to $1.32, due to lower interest expense and a lower share count, partially offset by a higher non-GAAP effective tax rate.

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"Our second quarter results demonstrate continued momentum against our plans, led by better-than-expected performance in the Pharmaceutical segment and Medical results in-line with our prior commentary," said Jason Hollar, CEO of Cardinal Health. "With the first half of fiscal year 2023 behind us, we are pleased to raise our full year non-GAAP EPS guidance and outlook for the Pharmaceutical segment. In the Medical segment, we remain confident in our Medical Improvement Plan, including the actions we are taking to mitigate supply chain inflation and drive improved performance."

Q2 FY23 summary

Q2 FY23

Q2 FY22

Y/Y

Revenue

$51.5 billion

$45.5 billion

13 %

Operating loss

$(119) million

$(950) million

(87) %

Non-GAAP operating earnings

$467 million

$467 million

— %

Net earnings/(loss) attributable to Cardinal Health, Inc.

$(130) million

$49 million

N.M.

Non-GAAP net earnings attributable to Cardinal Health, Inc.

$346 million

$357 million

(3) %

Effective Tax Rate2

5.4 %

105.0 %

Non-GAAP Effective Tax Rate

23.0 %

19.4 %

Diluted EPS attributable to Cardinal Health, Inc.

$(0.50)

$0.17

N.M.

Non-GAAP diluted EPS attributable to Cardinal Health, Inc.

$1.32

$1.27

4 %

Segment results

Pharmaceutical segment

Q2 FY23

Q2 FY22

Y/Y

Revenue

$ 47.7 billion

$ 41.4 billion

15 %

Segment profit

$ 464 million

$ 426 million

9 %

Second-quarter revenue for the Pharmaceutical segment increased 15% to $47.7 billion, driven by brand and specialty pharmaceutical sales growth from existing and net new customers.

Pharmaceutical segment profit increased 9% to $464 million in the second quarter, driven by a higher contribution from brand and specialty products and generics program performance, partially offset by inflationary supply chain costs.

Medical segment

Q2 FY23

Q2 FY22

Y/Y

Revenue

$ 3.8 billion

$ 4.1 billion

(7) %

Segment profit

$ 17 million

$ 50 million

(66) %

Second-quarter revenue for the Medical segment decreased 7% to $3.8 billion, driven by lower Products and Distribution sales, including PPE pricing and volumes. Growth in at-Home Solutions partially offset this decline.

Medical segment profit decreased 66% to $17 million in the second quarter, primarily due to lower Products and Distribution volumes and net inflationary impacts, partially offset by an improvement in PPE margins.

Fiscal year 2023 outlook1
The company updated its fiscal year 2023 guidance range for non-GAAP diluted earnings per share attributable to Cardinal Health, Inc. to $5.20 to $5.50, from $5.05 to $5.40.

This guidance includes an update to fiscal year 2023 Pharmaceutical segment profit outlook to 4% to 6.5% growth, from 2% to 5% growth. Additionally, the company updated expectations for fiscal year 2023 interest and other to $115 million to $130 million, from $140 million to $160 million.

The company does not provide forward-looking guidance on a GAAP basis as certain financial information, the probable significance of which cannot be determined, is not available and cannot be reasonably estimated. See "Use of Non-GAAP Measures" following the attached schedules for additional explanation.

Investor Day
The company plans to host an Investor Day on June 8 in New York City to discuss its long-term financial outlook, growth strategies, and conclusions from the Business Review Committee’s comprehensive review. The event will be live-webcast and archived on Cardinal Health’s Investor Relations website.

Recent highlights

Cardinal Health and its board of directors announced that Aaron Alt will become the company’s new chief financial officer (CFO) effective February 10. Alt most recently served as EVP and CFO for Sysco Corporation, the leading global food service distribution company.
Cardinal Health released its fiscal year 2022 Environmental, Social, and Governance (ESG) report which reflects significant progress in ESG efforts and highlights the company’s commitment to helping build a more sustainable, equitable world, and a healthier future for employees, customers and communities.
Cardinal Health completed its $1 billion dollar accelerated share repurchase (ASR) program and initiated a new $250 million dollar ASR program in the second quarter, resulting in a total of $1.25 billion year-to-date share repurchases in fiscal year 2023.
Cardinal Health announced the launch of Velocare, a supply chain network and last-mile fulfillment solution capable of reaching patients in one to two hours with critical products and services required for hospital-level care at home. Through a strategic collaboration with Medically Home, Cardinal Health at-Home Solutions is now supporting a Medically Home health system customer with Velocare, collectively enabling scaled, high-acuity care in the home.
Cardinal Health’s U.S. Medical Products and Distribution business opened its expanded Sustainable Technologies facility in Riverview, Florida, doubling the manufacturing facility to roughly 100,000 square feet. Sustainable Technologies is a leading provider of single-use device collections, reprocessing and recycling services in the U.S., helping to deliver supply resiliency, sustainable solutions, and cost savings for customers.
Webcast
Cardinal Health will host a webcast today at 8:30 a.m. Eastern to discuss second-quarter results. To access the webcast and corresponding slide presentation, go to the Investor Relations page at ir.cardinalhealth.com. No access code is required.

Presentation slides and a webcast replay will be available on the Investor Relations page for 12 months.

ArcticZymes Technologies Q4, full year 2022 results and extended investor presentation

On February 2, 2023 ArcticZymes Technologies (OSE: AZT) reported sales of NOK 28.2 million (40.5) and an EBITDA of NOK 1.3 million (20.8) for the fourth quarter of 2022 (Press release, ArcticZymes Technologies, FEB 2, 2023, View Source [SID1234626759]).

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Highlights from Q4 and the full year 2022

ArcticZymes Technologies (AZT) had Q4 sales of NOK 28.2 million a reduction of 30% (Q4 2021: NOK 40.5 million) and sales for the full year of NOK 137.0 million growing by 7% (12M 2021: NOK 128.0 million)
AZT had a positive EBITDA for Q4 of NOK 1.3 million, a reduction of NOK 19.5 million (Q4 2021: NOK 20.8 million) and a positive EBITDA for 2022 of NOK 41.5 million, a reduction of 20.1 million (12M 2021: NOK 61.6 million).
Operating expenses for Q4 were 26.0 million (Q4 2021: NOK 18.4 million) impacted by one-off expenditure. Operating expenses for 2022 totalled NOK 91.0 (12M 2021: NOK 65.5 million)
Cash flow for Q4 was positive NOK 5.6 million (Q4 2021: NOK 14.0 million) giving a cash balance of NOK 244.2 million (Q4 2021: NOK 200.4 million)
Launched 3 new products: AZscriptTM Reverse Transcriptase; SAN HQ 2.0 ELISA kit & ArcticZymes Proteinase Glycerol FREE
Upscaled the manufacturing capacity of AZ Proteinase to meet growing demand
Signed exclusive license deal for a novel DNA assembly technology to expand offerings in both the molecular tools and biomanufacturing businesses
Conducted a comprehensive M&A process and engaged in negotiations with a European company. As a result of due diligence findings however, AZT terminated the acquisition process

Ashvattha Therapeutics to Present at Upcoming Investor Conferences

On February 2, 2023 Ashvattha Therapeutics ("Ashvattha"), a clinical-stage company leveraging its nanomedicine technology, hydroxyl dendrimers (HDs), to develop a new class of precision medicines, reported that the Company will provide a corporate overview at two upcoming investor conferences (Press release, Ashvattha Therapeutics, FEB 2, 2023, View Source [SID1234626758]). The corporate overview will highlight the company’s innovative approach to precision nanomedicine through its proprietary hydroxyl dendrimer therapies.

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Details for the presentations are as follows:

2023 BIO CEO & Investor Conference
Date: Monday, February 6, 2023
Time: 2:15 PM ET
Location: Palace Room, Marriott Marquis, New York, and virtual
Biocom California’s 13th Annual Global Life Science Partnering & Investor Conference
Date: Wednesday, March 1, 2023
Time: 4:09 PM PT
Location: Charles Fries Room, The Lodge at Torrey Pines, La Jolla, California
Jeffrey Cleland, Ph.D., Chairman, Chief Executive Officer, and President of Ashvattha will be available for one-on-one meetings onsite with registered attendees.

Anaveon doses first patient in a Phase I/II Study of ANV419 as monotherapy or in combination with check point inhibitors in patients with advanced melanoma

On February 2, 2023 Anaveon, a clinical stage, immuno-oncology company, reported the first patient has been dosed in the OMNIA-1 study – a Phase I/II study assessing the efficacy and safety of ANV419 for the treatment of advanced melanoma. ANV419 is a powerful, IL-2Rbeta selective IL-2 agonist, which has been specifically designed to enable the delivery of high dose IL-2 (Press release, Anaveon, FEB 2, 2023, View Source [SID1234626757]).

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"In the first-in-human study, the data demonstrate the ability of ANV419 to be delivered at high molar equivalents of IL-2 in a tolerable and convenient way, with preferential stimulation and expansion of NK and CD8+ T cells," said Eduard Gasal, MD, Chief Medical Officer at Anaveon. "We are excited to continue the development of our next-generation IL-2 in patients with advanced melanoma."

In the past decade, there has been steady progress in the development of targeted therapy and immunotherapy for metastatic cutaneous melanoma with a substantial increase in the 5‑year overall survival (OS) rates from less than 10% to up to 50%. Despite substantial progress, 30% to 70% of patients do not respond to initial anti-programmed death 1/ligand 1 (PD-1/L1) therapy, and approximately 25% eventually progress. Thus, the overall outlook for patients with metastatic cutaneous melanoma remains challenging and the development of new effective and tolerable therapy is needed1.

About the OMNIA-1 study
This global, open label, randomized, parallel arm, Phase I/II study (ANV419-101) will enrol up to 130 patients with advanced cutaneous melanoma. The study consists of a monotherapy dose expansion part, followed by a combination part of ANV419 with anti-PD1 or anti-CTLA-4 in patients who have progressed on or following standard of care immunotherapy2.

Anaveon expects to report initial safety and efficacy data of the OMNIA-1 study by early 2024.

Anaveon is conducting several Phase I/II trials in parallel in solid tumors and hematological malignancies. In addition, Anaveon continues its work in developing follow-on compounds to expand on the success of ANV419 by delivering the IL-2 agonist to tumor fighting cells and expand into less immunogenic tumors. The Company is building on its cytokine engineering expertise with preclinical-stage programs harnessing the power of cytokines for therapeutic purposes.