AstraZeneca’s Full Year and Q4 2024 results
Strong momentum in FY 2024 with Total Revenue and Core EPS up 21% and 19% respectively
CAMBRIDGE, England–(BUSINESS WIRE)–
AstraZeneca:
Revenue and EPS summary
|
|
|
FY 2024 |
% Change |
Q4 2024 |
% Change |
||||
|
$m |
Actual |
CERi |
$m |
Actual |
CER |
||||
|
– Product Sales |
50,938 |
16 |
19 |
13,362 |
18 |
19 |
|||
|
– Alliance Revenue |
|
2,212 |
55 |
55 |
714 |
68 |
69 |
||
|
– Collaboration Revenue |
923 |
56 |
54 |
815 |
>2x |
>2x |
|||
|
Total Revenue |
|
54,073 |
18 |
21 |
14,891 |
24 |
25 |
||
|
Reported EPS |
$4.54 |
18 |
29 |
$0.97 |
56 |
71 |
|||
|
Coreii EPS |
$8.21 |
13 |
19 |
$2.09 |
44 |
49 |
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Financial performance for FY 2024 (Growth numbers at constant exchange rates)
Total Revenue up 21% to $54,073m, driven by a 19% increase in Product Sales, continued growth of partnered medicines (Alliance Revenue) and the achievement of sales-based milestones (Collaboration Revenue)
Total Revenue growth from Oncology was 24%, CVRM 20%, R&I 25%, V&I 8% and Rare Disease 16%
Core EPS increased 19% to $8.21
Second interim dividend declared of $2.10 per share, making a total annual dividend declared for FY 2024 of $3.10 per share, an increase of 7%. Dividend to be further increased in FY 2025
Guidance for FY 2025: Total Revenue is expected to increase by a high single-digit percentage and Core EPS is expected to increase by a low double-digit percentage, both at CER
Pascal Soriot, Chief Executive Officer, AstraZeneca, said:
“Our company delivered a very strong performance in 2024 with Total Revenue and Core EPS up 21% and 19% respectively. We also delivered nine positive high value Phase III studies in the year, which coupled with increasing demand for our medicines in all key regions, will help sustain our growth momentum into 2025.
This year marks the beginning of an unprecedented, catalyst-rich period for our company, an important step on our Ambition 2030 journey to deliver $80 billion Total Revenue by the end of the decade. In 2025 alone, we anticipate the first Phase III data for seven new medicines, along with several important new indication opportunities for our existing medicines.
We are also investing in and making significant progress with transformative technologies that have the potential to drive our growth well beyond 2030, many of which have now entered pivotal trials.”
Key milestones achieved since the prior results announcement
Positive read-outs for Truqap in combination with abiraterone and androgen deprivation therapy in PTEN-deficient de novo metastatic hormone-sensitive prostate cancer (CAPItello-281) and Tagrisso with or without chemotherapy in resectable early-stage EGFRm NSCLC (NeoADAURA)
US approvals for Imfinzi in limited-stage small cell lung cancer (ADRIATIC), Calquence in combination with bendamustine and rituximab in mantle cell lymphoma (ECHO), Datroway (datopotamab deruxtecan) in HR+ HER2- metastatic breast cancer (TROPION-Breast01) and Enhertu in chemotherapy-naïve HER2-low and -ultralow metastatic breast cancer (DESTINY-Breast06). EU approvals for Tagrisso in unresectable EGFRm NSCLC (LAURA) and Kavigale for prevention of COVID-19 (SUPERNOVA). Japan approvals for Imfinzi in endometrial cancer (DUO-E), Lynparza plus Imfinzi in pMMR endometrial cancer (DUO-E), Calquence tablet formulation in chronic / small lymphocytic leukaemia, Datroway in HR+ HER2- metastatic breast cancer, Fasenra in EGPA (MANDARA) and Kavigale for prevention of COVID-19. China approvals for Lynparza in gBRCAm HER2- early breast cancer (OlympiA), Orpathys in locally advanced or metastatic MET Exon 14 NSCLC (NCT04923945)
Guidance
The Company issues its Total Revenue and Core EPS guidance for FY 2025 at CER, based on the average foreign exchange rates through 2024.
|
|
Total Revenue is expected to increase by a high single-digit percentage
Core EPS is expected to increase by a low double-digit percentage
|
|
The Core Tax rate is expected to be between 18-22%
The Company is unable to provide guidance on a Reported basis because it cannot reliably forecast material elements of the Reported results, including any fair value adjustments arising on acquisition-related liabilities, intangible asset impairment charges and legal settlement provisions. Please refer to the cautionary statements section regarding forward-looking statements at the end of this announcement.
Currency impact
If foreign exchange rates for February 2025 to December 2025 were to remain at the average rates seen in January 2025, it is anticipated that Total Revenue in FY 2025 would incur a low single-digit percentage adverse impact compared to the performance at CER, and Core EPS would incur a mid-single-digit percentage adverse impact. The Company’s foreign exchange rate sensitivity analysis is provided in Table 17.
Capital allocation
In FY 2025, the Company intends to increase the annual dividend declared to $3.20 per share. The Company also expects to increase capital expenditureiii by approximately 50%, driven by manufacturing expansion projects and investment in IT systems, to support portfolio growth and build capacity for transformative technologies.
China
In relation to the illegal drug importation allegations, in January 2025, AstraZeneca received a Notice of Transfer to the Prosecutor and an Appraisal Opinion from the Shenzhen City Customs Office regarding suspected unpaid importation taxes amounting to $0.9 million. To the best of AstraZeneca’s knowledge, the importation taxes referred to in the Appraisal Opinion relate to Imfinzi and Imjudo. A fine of between one and five times the amount of unpaid importation taxes may also be levied if AstraZeneca is found liable. AstraZeneca continues to fully cooperate with the Chinese authorities.
In December 2024 AstraZeneca announced the appointment of Iskra Reic as Executive Vice President, International, which encompasses China, Asian and Eurasian markets, Middle East & Africa, Latin America, Australia & New Zealand. Iskra succeeds Leon Wang who is on extended leave from the Company while under investigation in China.
Table 1: Key elements of Total Revenue performance in Q4 2024
|
% Change |
||||||
|
Revenue type |
|
$m |
Actual % |
CER % |
|
|
|
Product Sales |
13,362 |
18 |
19 |
|
|
|
|
Alliance Revenue |
|
714 |
68 |
69 |
|
$392m Enhertu (Q4 2023: $281m) $133m Tezspire (Q4 2023: $80m) $161m Beyfortus (Q4 2023: $41m) |
|
Collaboration Revenue |
815 |
>2x |
>2x |
|
$600m Lynparza (Q4 2023: $245m) $111m Beyfortus (Q4 2023: $27m) $100m Koselugo (Q4 2023: nil) |
|
|
Total Revenue |
|
14,891 |
24 |
25 |
|
|
|
Therapy areas |
$m |
Actual % |
CER % |
|
|
|
|
Oncology |
6,344 |
27 |
29 |
|
Tagrisso up 20% (21% at CER), Calquence up 20%, Enhertu up 48% (54% at CER) |
|
|
CVRM |
3,138 |
16 |
17 |
|
Farxiga up 21% (22% at CER),Lokelma up35% |
|
|
R&I |
|
2,127 |
27 |
28 |
|
Breztri up 29%. Saphnelo up 65%, Tezspire up 86% (85% at CER), Symbicort up 31% (33% CER) |
|
V&I |
|
651 |
58 |
55 |
|
Beyfortus Total Revenue up >3x |
|
Rare Disease |
|
2,377 |
21 |
22 |
|
Ultomiris up 32% (33% at CER), partially offset by decline in Soliris of 24% (22% at CER), Strensiq up 38% (37% at CER) and Koselugo up >3x |
|
Other Medicines |
|
254 |
(7) |
(6) |
|
|
|
Total Revenue |
|
14,891 |
24 |
25 |
|
|
|
Regions |
|
$m |
Actual % |
CER % |
|
|
|
US |
6,532 |
28 |
28 |
|
Product Sales up 25% |
|
|
Emerging Markets |
|
3,134 |
13 |
19 |
|
|
|
– China |
1,364 |
(1) |
(3) |
|
Decline primarily due to low rates of seasonal respiratory viral infections, and impact from year-end hospital budget dynamics |
|
|
– Ex-China Emerging Markets |
|
1,770 |
26 |
42 |
|
|
|
Europe |
|
3,948 |
37 |
35 |
|
Product Sales up 20% (18% at CER) |
|
Established RoW |
|
1,277 |
1 |
2 |
|
|
|
Total Revenue |
|
14,891 |
24 |
25 |
|
|
Key alliance medicines
Combined sales of Enhertu, recorded by Daiichi Sankyo Company Limited (Daiichi Sankyo) and AstraZeneca, amounted to $3,754m in FY 2024 (FY 2023: $2,566m)
Combined sales of Tezspire, recorded by Amgen and AstraZeneca, amounted to $1,219m in FY 2024 (FY 2023: $653m)
Table 2: Key elements of financial performance in Q4 2024
|
Metric |
Reported |
Reported |
Core |
Core |
|
Commentsiv |
|
Total Revenue |
$14,891m |
24% Actual |
$14,891m |
24% Actual |
|
See Table 1 and the Total Revenue section of this document for further details |
|
Product Sales Gross Margin |
80% |
Stable Actual |
79% |
-1pp Actual |
|
Variations in Product Sales Gross Margin can be expected between periods, due to product seasonality, foreign exchange fluctuations and other effects |
|
R&D expense |
$4,677m |
52% Actual |
$3,573m |
23% Actual |
|
Increased investment in the pipeline
Core R&D-to-Total Revenue ratio of 24% |
|
SG&A expense |
$5,410m |
1% Actual |
$4,275m |
6% Actual |
|
Market development for recent launches and pre-launch activities |
|
Other operating income and expensev |
$100m |
-7% Actual |
$101m |
-7% Actual |
|
|
|
Operating Margin |
14% |
+3pp Actual |
28% |
+5pp Actual |
|
See commentary above on Gross Margin, R&D, SG&A and Other operating income and expense |
|
Net finance expense |
$365m |
9% Actual |
$310m |
20% Actual |
|
Recent debt issued at higher interest rates |
|
Tax rate |
10% |
+17pp Actual |
16% |
+7pp Actual |
|
Variations in the tax rate can be expected between periods |
|
EPS |
$0.97 |
56% Actual |
$2.09 |
44% Actual |
|
Further details of differences between Reported and Core are shown in Table 12 |
Table 3: Pipeline highlights since prior results announcement
|
Event |
Medicine |
Indication / Trial |
Event |
|
Regulatory approvals and other regulatory actions |
Tagrisso |
EGFRm NSCLC (Stage III unresectable) (LAURA) |
Regulatory approval (EU, CN) |
|
Imfinzi |
Limited-stage SCLC (ADRIATIC) |
Regulatory approval (EU) |
|
|
Imfinzi |
Advanced endometrial cancer |
Regulatory approval (JP) |
|
|
Calquence |
Tablets for chronic lymphocytic leukaemia |
Regulatory approval (JP) |
|
|
Calquence |
Mantle cell lymphoma (1st-line) (ECHO) |
Regulatory approval (US) |
|
|
Lynparza + Imfinzi |
Advanced endometrial cancer with mismatch repair proficiency (DUO-E) |
Regulatory approval (JP) |
|
|
Lynparza |
gBRCAm HER2- eBC (OlympiA) |
Regulatory approval (CN) |
|
|
Enhertu |
HR+ HER2-low and -ultralow mBC (DESTINY-Breast06) |
Regulatory approval (US) |
|
|
Datroway |
HR+ HER2- mBC (TROPION-Breast01) |
Regulatory approval (JP, US) |
|
|
Orpathys |
MET exon 14 skipping altered NSCLC (NCT04923945) |
Regulatory approval (CN) |
|
|
Fasenra |
EGPA (MANDARA) |
Regulatory approval (JP) |
|
|
Kavigale |
Prevention of COVID-19 (SUPERNOVA) |
Regulatory approval (EU, JP) |
|
|
|
|
|
|
|
Regulatory submissions or acceptances* |
Imfinzi |
Muscle-invasive bladder cancer (NIAGARA) |
Regulatory submission (US, JP) |
|
Imfinzi + Imjudo |
NSCLC (1st-line) (POSEIDON) |
Regulatory submission (CN) |
|
|
Calquence |
Chronic lymphocytic leukaemia (1st-line) (AMPLIFY) |
Regulatory submission (EU) |
|
|
Datroway |
EGFRm NSCLC (later line) (TROPION-Lung05) |
Regulatory submission (US) |
|
|
Tezspire |
Severe uncontrolled asthma (NAVIGATOR/ DIRECTION) |
Regulatory submission (CN) |
|
|
Koselugo |
Neurofibromatosis type 1 adult (KOMET) |
Regulatory submission (EU, JP) |
|
|
|
|
|
|
|
Phase III / registrational data readouts and other developments |
Tagrisso |
Resectable early-stage EGFRm NSCLC(NeoADAURA) |
Primary endpoint met |
|
Truqap |
PTEN-deficient de novo metastatic hormone-sensitive prostate cancer (CAPItello-281) |
Primary endpoint met |
|
|
|
|
|
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|
*US, EU and China regulatory submission denotes filing acceptance |
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Other pipeline updates
In January 2025, the vemircopan (ALXN2050) Phase II development programme was terminated. The decision was based on safety and efficacy data from Phase II trials.
Upcoming pipeline catalysts
For recent trial starts and anticipated timings of key trial readouts, please refer to the Clinical Trials Appendix, available on www.astrazeneca.com/investor-relations.html.
Sustainability highlights
The Company convened an event on health equity for investors and analysts in November that detailed AstraZeneca’s health equity strategy, which is embedded from the Company’s science through to healthcare delivery and community engagement.
At the end of 2024, the Company’s cumulative reduction in Scope 1 and 2 greenhouse gas (GHG) emissions was 77.5% from the 2015 baseline.
Conference call
A conference call and webcast for investors and analysts will begin today, 6 February 2025, at 11:00 UK time. Details can be accessed via astrazeneca.com.
Reporting calendar
The Company intends to publish its Q1 2025 results on 29 April 2025.
To read AstraZeneca’s Full Year and Q4 2024 Financial Results press release in full, click here.
View source version on businesswire.com: https://www.businesswire.com/news/home/20250205200649/en/
Global Media Relations team
[email protected]
+44 (0)1223 344 800
KEYWORDS: United Kingdom Europe
INDUSTRY KEYWORDS: Oncology Health Infectious Diseases Pharmaceutical Cardiology Biotechnology
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