Lilly Reports Fourth-Quarter 2022 Financial Results, Core Business Growth and Pipeline Advancements Support Strong Long-Term Outlook

On February 2, 2023 Eli Lilly and Company (NYSE: LLY) reported its financial results for the fourth quarter of 2022 (Press release, Eli Lilly, FEB 2, 2023, View Source [SID1234626764]).

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"2023 is an inflection point for Lilly – a chance to expand our impact on patients and growth potential as an R&D-driven biopharma company," said David A. Ricks, Lilly’s chair and CEO. "Over the course of this critical year, we hope to launch as many as four new medicines for challenging diseases, while advancing our next generation of molecules currently in Phase 3."

Anat Ashkenazi, Lilly’s executive vice president and chief financial officer added: "As we closed out 2022, Lilly demonstrated strong growth and achieved meaningful pipeline progress that included the launch for Mounjaro in type 2 diabetes. We expect to capitalize on this momentum and deliver mid-teen revenue growth for our core business in 2023 while remaining committed to investing in innovation, late-stage opportunities, manufacturing capacity, and our people."

Lilly shared numerous updates recently on key regulatory, clinical, business development and other events, including:

The U.S. Food and Drug Administration (FDA) approval of Jaypirca (pirtobrutinib) for adults with relapsed or refractory mantle cell lymphoma after at least two lines of systemic therapy, including a BTK inhibitor, under the accelerated approval pathway;
FDA issuance of a complete response letter for the accelerated approval submission of donanemab for early Alzheimer’s disease;
FDA and European Medicines Agency acceptance of regulatory submissions for Jardiance for adults with chronic kidney disease based on results from the EMPA-KIDNEY Phase 3 trial;
The initiation of a rolling submission in the U.S. for tirzepatide in obesity and FDA Fast Track designation for tirzepatide in obstructive sleep apnea;
The announcement that Jardiance is the first SGLT2 inhibitor to show statistically significant reduction in blood sugar levels in children and adolescents with type 2 diabetes;
Positive donanemab data from the first Phase 3 active comparator study in early Alzheimer’s disease, TRAILBLAZER-ALZ 4;
Plans to invest an additional $450 million and create at least 100 new jobs to expand manufacturing capacity at the company’s Research Triangle Park facility;
The acquisition of Akouos, Inc., which expands Lilly’s efforts in genetic medicines to include Akouos’s potential first-in-class adeno-associated viral gene therapies;
The fifth consecutive 15% annual increase in Lilly’s quarterly dividend, doubling since 2018;
A collaboration with EVA Pharma to establish local manufacturing capabilities to supply low-cost insulin to at least 1 million people by 2030, mostly in Africa; and
An initiative with Direct Relief to expand cold chain capacity in Africa, Latin America, the Caribbean and Southeast Asia.
For additional information on these and other important public announcements, visit the news section of Lilly’s website.

Financial Results

$ in millions, except

per share data

Fourth Quarter

%

2022

2021

Change

Revenue

$7,301.8

$7,999.9

(9) %

Net Income – Reported

1,937.7

1,726.1

12 %

EPS – Reported

2.14

1.90

13 %

Net Income – Non-GAAP

1,893.1

1,970.5

(4) %

EPS – Non-GAAP

2.09

2.17

(4) %

A discussion of the non-GAAP financial measures is included under "Reconciliation of GAAP Reported to Selected Non-GAAP Adjusted Information (Unaudited)."

Fourth-Quarter Reported Results

In Q4 2022, worldwide revenue was $7.30 billion, a decrease of 9% compared with Q4 2021, driven by a 4% decrease from the unfavorable impact of foreign exchange rates, a 3% decrease due to lower realized prices, and a 2% decrease in volume. Excluding COVID-19 antibodies, revenue in Q4 2022 increased 5% and total worldwide volume increased 13%. Key growth products, consisting of Verzenio, Mounjaro, Jardiance, Taltz, Trulicity, Retevmo, Emgality, Cyramza, Tyvyt and Olumiant, grew 21% and represented 70% of revenue for Q4 2022.

Revenue in the U.S. decreased 10% to $4.66 billion, driven by a 10% decrease in volume with prices remaining relatively flat. Excluding revenue from COVID-19 antibodies, revenue in the U.S. increased by 11%, primarily driven by volume from key growth products.

Revenue outside the U.S. decreased 6% to $2.64 billion, driven by a 12% decrease from the unfavorable impact of foreign exchange rates and a 7% decrease due to lower realized prices, partially offset by a 12% increase in volume. The lower realized prices were primarily driven by the impact of government pricing in China from the volume-based procurement (VBP) for Humalog and the National Reimbursement Drug List (NRDL) formulary for certain products, particularly Verzenio and Tyvyt. The increase in volume outside the U.S. was largely driven by key growth products and approximately $130 million of one-time revenue associated with the sale of the company’s rights to Alimta in Korea and Taiwan.

Gross margin decreased 3% to $5.75 billion in Q4 2022 compared with Q4 2021. Gross margin as a percent of revenue was 78.8%, an increase of 4.4 percentage points compared with Q4 2021. The increase in gross margin percent was primarily driven by lower sales of COVID-19 antibodies, partially offset by lower realized prices and increased expenses due to inflation and logistics costs.

In Q4 2022, research and development expenses increased 5% to $2.00 billion, or 27% of revenue, driven by higher development expenses for late-stage assets, partially offset by the favorable impact of foreign exchange rates and lower development expenses for COVID-19 antibodies.

Marketing, selling and administrative expenses increased 3% to $1.64 billion in Q4 2022, primarily driven by costs associated with launches of new products and indications, partially offset by the favorable impact of foreign exchange rates.

In Q4 2022, the company recognized acquired in-process research and development (IPR&D) and development milestone charges of $240.1 million. In Q4 2021, the company recognized acquired IPR&D and development milestone charges of $437.7 million, primarily related to a business development transaction with Foghorn Therapeutics Inc.

In Q4 2022, the company recognized asset impairment, restructuring and other special charges of $38.1 million, primarily related to acquisition and integration costs associated with the closing of our acquisition of Akouos, Inc. In Q4 2021, the company recognized asset impairment, restructuring and other special charges of $104.5 million, primarily related to impairment of an intangible asset from our acquisition of Loxo Oncology.

Operating income in Q4 2022 was $1.84 billion compared with $1.92 billion in Q4 2021. Operating margin percent, defined as operating income as a percent of revenue, was 25.1%, which includes a negative impact of approximately 330 basis points attributed to acquired IPR&D and development milestone charges.

Other income (expense) was income of $260.0 million in Q4 2022 compared with expense of $77.3 million in Q4 2021. The increase in other income (expense) was primarily driven by net gains on investments in equity securities in Q4 2022 compared with net losses on investments in equity securities in Q4 2021.

The effective tax rate was 7.6% in Q4 2022 compared with 6.2% in Q4 2021. The effective tax rate in Q4 2022 reflects the favorable tax impact of the implementation of the provision in the Tax Cuts and Jobs Act (the 2017 Tax Act) that requires capitalization and amortization of research and development expenses for tax purposes starting in 2022 and a net discrete tax benefit, partially offset by the tax impact of the mix of earnings in higher tax jurisdictions. The effective tax rate in Q4 2021 reflected a net discrete tax benefit and the tax impact of acquired IPR&D and development milestone charges.

In Q4 2022, net income and earnings per share (EPS) were $1.94 billion and $2.14, respectively, compared with $1.73 billion and $1.90 in Q4 2021. Q4 2022 EPS was inclusive of $0.23 of acquired IPR&D and development milestone charges compared with $0.39 in Q4 2021.

Fourth-Quarter Non-GAAP Measures

On a non-GAAP basis, Q4 2022 gross margin decreased 3% to $5.88 billion compared with Q4 2021. Gross margin as a percent of revenue was 80.5%, an increase of 4.4 percentage points compared with Q4 2021. The increase in gross margin percent was primarily driven by lower sales of COVID-19 antibodies, partially offset by lower realized prices and increased expenses due to inflation and logistics costs.

Operating income on a non-GAAP basis decreased $160.5 million, or 7%, to $2.00 billion in Q4 2022 compared with Q4 2021. Operating margin percent was 27.4% on a non-GAAP basis, which includes a negative impact of approximately 330 basis points attributed to acquired IPR&D and development milestone charges.

The effective tax rate on a non-GAAP basis was 7.3% in Q4 2022 compared with 8.5% in Q4 2021. The lower effective tax rate for Q4 2022 reflects the favorable tax impact of the implementation of the 2017 Tax Act and a higher net discrete tax benefit compared to the same period in 2021, partially offset by the tax impact of the mix of earnings in higher tax jurisdictions.

On a non-GAAP basis, Q4 2022 net income and EPS were $1.89 billion and $2.09, respectively, compared with $1.97 billion and $2.17 in Q4 2021. Q4 2022 non-GAAP EPS was inclusive of $0.23 of acquired IPR&D and development milestone charges compared with $0.39 in Q4 2021.

For further detail on non-GAAP measures, see the reconciliation below as well as the "Reconciliation of GAAP Reported to Selected Non-GAAP Adjusted Information (Unaudited)" table later in this press release.

Fourth Quarter

2022

2021

% Change

Earnings per share (reported)

$ 2.14

$ 1.90

13 %

Amortization of intangible assets

.11

.19

Asset impairment, restructuring and other special charges

.03

.09

Net (gains) losses on investments in equity securities

(.19)

.06

Partial reversal of COVID-19 antibodies inventory charges

(.07)

Earnings per share (non-GAAP)

$ 2.09

$ 2.17

(4) %

Numbers may not add due to rounding.

Acquired IPR&D and development milestone charges

.23

.39

(41) %

Selected Revenue Highlights

(Dollars in millions)

Fourth Quarter

Full Year

Selected Products

2022

2021

% Change

2022

2021

% Change

Trulicity

$ 1,936.2

$ 1,883.7

3 %

$ 7,439.7

$ 6,471.9

15 %

Verzenio

808.0

404.1

100 %

2,483.5

1,349.9

84 %

Taltz

707.8

647.4

9 %

2,482.0

2,212.8

12 %

Jardiance(a)

612.3

431.9

42 %

2,066.0

1,490.8

39 %

Humalog(b)

548.3

601.7

(9) %

2,060.6

2,453.0

(16) %

COVID-19 antibodies(c)

38.0

1,063.1

(96) %

2,023.5

2,239.3

(10) %

Humulin

234.0

298.8

(22) %

1,019.4

1,222.6

(17) %

Cyramza

277.8

270.4

3 %

971.4

1,033.0

(6) %

Alimta

236.6

434.9

(46) %

927.7

2,061.4

(55) %

Olumiant(d)

205.8

306.0

(33) %

830.5

1,115.1

(26) %

Basaglar

201.7

242.4

(17) %

760.4

892.5

(15) %

Emgality

175.6

161.5

9 %

650.9

577.2

13 %

Forteo

160.0

184.0

(13) %

613.1

801.9

(24) %

Mounjaro

279.2

NM

482.5

NM

Tyvyt

57.5

77.8

(26) %

293.3

418.1

(30) %

Retevmo

64.6

38.6

67 %

191.9

114.7

67 %

Total Revenue

7,301.8

7,999.9

(9) %

28,541.4

28,318.4

1 %

(a) Jardiance includes Glyxambi, Synjardy and Trijardy XR

(b) Humalog includes Insulin Lispro

(c) COVID-19 antibodies include sales for bamlanivimab administered alone, for bamlanivimab and etesevimab
administered together, and for bebtelovimab, and were made pursuant to EUAs or similar regulatory authorizations

(d) Olumiant includes sales of baricitinib that were made pursuant to EUA or similar regulatory authorizations

NM – not meaningful

Trulicity

For Q4 2022, worldwide Trulicity revenue was $1.94 billion, an increase of 3% compared with Q4 2021. U.S. revenue increased 5% to $1.53 billion, driven by increased demand, partially offset by lower realized prices. Revenue outside the U.S. was $409.8 million, a decrease of 6%, driven by the unfavorable impact of foreign exchange rates and to a lesser extent, lower realized prices, partially offset by increased demand. On a constant currency basis, revenue outside the U.S. increased 8%. Lilly experienced intermittent delays in fulfilling certain U.S. Trulicity orders during Q4 2022. Actions to manage strong demand across the company’s incretin portfolio, including measures to minimize existing patient impact in international markets, also affected volume.

Verzenio

For Q4 2022, worldwide Verzenio revenue increased 100% compared with Q4 2021 to $808.0 million. U.S. revenue was $552.7 million, an increase of 119%, primarily driven by increased demand. Revenue outside the U.S. was $255.3 million, an increase of 69%, driven by increased demand, partially offset by the unfavorable impact of foreign exchange rates and lower realized prices primarily due to the impact of the NRDL formulary in China.

Taltz

For Q4 2022, worldwide Taltz revenue increased 9% compared with Q4 2021 to $707.8 million. U.S. revenue increased 9% to $512.0 million, driven by increased demand, partially offset by lower realized prices. Revenue outside the U.S. increased 11% to $195.8 million, driven by increased volume, partially offset by the unfavorable impact of foreign exchange rates and lower realized prices.

Jardiance

The company’s worldwide Jardiance revenue for Q4 2022 was $612.3 million, an increase of 42% compared with Q4 2021. U.S. revenue increased 51% to $363.1 million, primarily driven by increased demand and to a lesser extent, an increased Q4 2022 royalty from Boehringer Ingelheim for exceeding certain annual thresholds. Revenue outside the U.S. was $249.2 million, an increase of 30%, primarily driven by increased demand, partially offset by the unfavorable impact of foreign exchange rates.

Jardiance is part of the company’s alliance with Boehringer Ingelheim. Lilly reports as revenue royalties received on net sales of Jardiance.

Humalog

For Q4 2022, worldwide Humalog revenue decreased 9% compared with Q4 2021 to $548.3 million. U.S. revenue increased 8% to $336.0 million, driven by higher realized prices due to changes in estimates for rebates and discounts in both periods. Revenue outside the U.S. decreased 27% to $212.3 million, driven by lower realized prices due to the impact of VBP in China and the unfavorable impact of foreign exchange rates.

Alimta

For Q4 2022, worldwide Alimta revenue decreased 46% compared with Q4 2021 to $236.6 million. U.S. revenue decreased 83% to $53.2 million, driven by decreased demand due to generic competition. Revenue outside the U.S. increased 63% to $183.4 million, driven by approximately $130 million of one-time revenue associated with the sale of the company’s rights to Alimta in Korea and Taiwan, partially offset by decreased demand due to generic competition, lower realized prices, and the unfavorable impact of foreign exchange rates.

The company expects continued volume and revenue decline for Alimta as a result of generic competition due to the loss of patent exclusivity in major markets.

Olumiant

For Q4 2022, worldwide Olumiant revenue decreased 33% compared with Q4 2021 to $205.8 million. U.S. revenue decreased 50% to $43.5 million, driven by a decline in utilization for COVID-19 treatment, partially offset by increased utilization for the treatment of alopecia areata. Revenue outside the U.S. was $162.3 million, a decrease of 26%, driven by the unfavorable impact of foreign exchange rates and a decline in utilization for COVID-19 treatment.

Emgality

For Q4 2022, Emgality generated worldwide revenue of $175.6 million, an increase of 9% compared with Q4 2021. U.S. revenue was $132.0 million, an increase of 9%, driven by increased demand and higher realized prices, partially offset by wholesaler buying patterns. Revenue outside the U.S. was $43.7 million, an increase of 8%, primarily driven by increased volume, partially offset by the unfavorable impact of foreign exchange rates and lower realized prices.

Mounjaro

For Q4 2022, worldwide Mounjaro revenue was $279.2 million. U.S. revenue was $256.7 million. Mounjaro launched in the U.S. for the treatment of type 2 diabetes in June 2022.

Tyvyt

For Q4 2022, the company’s Tyvyt revenue in China was $57.5 million, a decrease of 26% compared with Q4 2021, driven by the impact of the NRDL formulary in China as well as increased competitive pressures and impacts from COVID-19 disruptions.

Tyvyt is part of the company’s alliance with Innovent. Lilly reports total sales of Tyvyt made by Lilly as revenue, with payments made to Innovent for its portion of the gross margin reported as cost of sales. Lilly also reports as revenue a portion of the gross margin for Tyvyt sales made by Innovent.

2023 Financial Guidance

The company has updated its tax rate and EPS guidance and reaffirmed all other elements of its 2023 financial guidance. The previous tax rate guidance of approximately 16% for 2023 assumed deferral or repeal of the 2017 Tax Act provision that requires capitalization of research and development expenses. Such a deferral or repeal did not occur in 2022. Given the uncertainty as to whether any change to this provision will be enacted in 2023, the company has updated the tax rate guidance to be approximately 13% and 2023 EPS guidance has been increased to the range of $7.90 to $8.10 on a reported basis and $8.35 to $8.55 on a non-GAAP basis. The company’s 2023 financial guidance reflects adjustments shown in the reconciliation table below.

2023

Expectations

Earnings per share (reported)

$7.90 to $8.10

Amortization of intangible assets

.45

Earnings per share (non-GAAP)

$8.35 to $8.55

Numbers may not add due to rounding

The company’s 2023 financial guidance does not include any acquired IPR&D and
development milestone charges either incurred or that may potentially be incurred in 2023.

The following table summarizes the company’s updated 2023 financial guidance:

2023 Guidance

Prior

Updated

Revenue

$30.3 to $30.8 billion

Unchanged

Gross Margin % of Revenue (reported)

Approx. 77%

Unchanged

Gross Margin % of Revenue (non-GAAP)

Approx. 79%

Unchanged

Marketing, Selling & Administrative

$6.9 to $7.1 billion

Unchanged

Research & Development

$8.2 to $8.4 billion

Unchanged

Other Income/(Expense)

$(200) to $(100) million

Unchanged

Tax Rate

Approx. 16%

Approx. 13%

Earnings per Share (reported)

$7.65 to $7.85

$7.90 to $8.10

Earnings per Share (non-GAAP)

$8.10 to $8.30

$8.35 to $8.55

Non-GAAP guidance reflects adjustments presented in the earnings per share table above.

Webcast of Conference Call

As previously announced, investors and the general public can access a live webcast of the Q4 2022 financial results conference call through a link on Lilly’s website at investor.lilly.com/webcasts-and-presentations. The conference call will begin at 10 a.m. Eastern time today and will be available for replay via the website.

Non-GAAP Financial Measures

Certain financial information for 2022 and 2021 is presented on both a reported and a non-GAAP basis. Some numbers in this press release may not add due to rounding. Reported results were prepared in accordance with U.S. generally accepted accounting principles (GAAP) and include all revenue and expenses recognized during the periods. Non-GAAP measures reflect adjustments for the items described in the reconciliation tables later in the release. This press release and related materials provide certain GAAP and non-GAAP figures excluding the impact of foreign exchange rates. Lilly recalculates current period figures on a constant currency basis by keeping constant the exchange rates from the base period. Beginning in 2022, presentations of non-GAAP financial measures do not include adjustments for upfront charges and development milestones related to acquired IPR&D. Non-GAAP financial measures for Q4 and fiscal year 2021 have been adjusted to reflect this updated presentation. The company’s 2023 financial guidance is being provided on both a reported and a non-GAAP basis. The non-GAAP measures are presented to provide additional insights into the underlying trends in the company’s business.

Deciphera Pharmaceuticals to Participate in Upcoming Investor Conferences

On February 2, 2023 Deciphera Pharmaceuticals, Inc. (NASDAQ: DCPH), a biopharmaceutical company focused on discovering, developing, and commercializing important new medicines to improve the lives of people with cancer, reported that members of the management team will participate in fireside chats at the following investor conferences (Press release, Deciphera Pharmaceuticals, FEB 2, 2023, View Source [SID1234626763]).

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Guggenheim Healthcare Talks Oncology Day on Thursday, February 9, 2023 at 10:45 AM ET in New York, NY
SVB Securities Global Biopharma Conference on Wednesday, February 15, 2023 at 3:00 PM ET (virtual)
A live webcast of both events will be available on the "Events and Presentations" page in the "Investors" section of the Company’s website at View Source A replay of both webcasts will be archived on the Company’s website for 90 days following the presentation.

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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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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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