Continued strong commercial performance and 12 positive Phase III programme readouts in the year to date
Revenue and EPS summary
| 9M 2026 | % Change | Q3 2026 | % Change | ||
| $m | Actual | CER1 | $m | Actual | CER |
- Product Sales | 43,962 | 7 | 5 | 15,066 | 5 | 5 |
- Alliance Revenue | 2,806 | 33 | 32 | 1,107 | 36 | 36 |
Product Revenue | 46,768 | 8 | 6 | 16,173 | 7 | 7 |
Collaboration Revenue | 113 | 22 | 23 | 36 | >3x | >3x |
Total Revenue | 46,881 | 8 | 7 | 16,209 | 7 | 7 |
Reported EPS ($) | 5.62 | 10 | 11 | 2.02 | 23 | 26 |
Core2 EPS ($) | 8.00 | 14 | 14 | 2.79 | 17 | 19 |
Key performance elements for 9M 2026
(Growth numbers at constant exchange rates)
- Total Revenue up 7%, with double-digit growth in Oncology, R&I and Rare Disease offsetting headwinds from Farxiga and Brilinta loss of exclusivity and volume-based procurement in
China - Core Operating profit and Core EPS increased 14%
- 47 approvals in major regions since Q4 2025 results, including first approvals for four new medicines (Etcamah, Baxfendy, Klygefa and Amlypave)
- First Phase III data for three NMEs (tozorakimab, efzimfotase alfa and sonesitatug vedotin)
“In the first nine months we saw strong commercial momentum with total revenue up 7% and Core EPS up 14%, driven by our diverse therapy areas and global presence. We have had approvals for four new medicines and reported 12 positive Phase III programme readouts with a collective peak year revenue potential well in excess of
With multiple potential blockbuster assets in late-stage development and transformative technologies scaling rapidly, we are on track to deliver our 2030 ambition and to sustain growth through the next decade.”
Guidance
Total Revenue is expected to increase by a mid-to-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%
If foreign exchange rates for
Results highlights
Table 1: Milestones achieved since the prior results announcement
Phase III and other registrational data readouts
Medicine | Trial | Indication | Event |
Enhertu | DESTINY-Lung04 | 1L HER2m NSCLC | Primary endpoint met |
Etcamah | SERENA-4 | 1L HR+ HER2- advanced breast cancer | Primary endpoint not met |
Imfinzi + tarlatamab | DeLLphi-305 | 1L ES-SCLC (maintenance) | Primary endpoint met |
Lynparza | MONO-OLA1 | 1L BRCAwt ovarian cancer | Dual primary endpoints met |
Tagrisso + Orpathys | SAFFRON | 2L+ EGFRm, MET-overexpressed and/or amplified NSCLC | Primary endpoint met |
Tagrisso + Orpathys | SANOVO | 1L EGFRm, MET-overexpressed NSCLC | Primary endpoint met |
volrustomig | eVOLVE-Lung02 | 1L PD-L1 <50% mNSCLC | Discontinued due to futility |
Tezspire | CROSSING | Eosinophilic esophagitis | Co-primary endpoints met |
Ultomiris | AWAKE | Delayed Graft Function | Discontinued due to lack of efficacy |
Regulatory approvals
Medicine | Trial | Indication | Region |
Datroway | TROPION-Breast02 | 1L TNBC for patients where immunotherapy is not an option | EU, JP, CN |
Enhertu | DESTINY-Breast09 | 1L HER2+ mBC | EU, JP, CN |
Enhertu | DESTINY-Breast05 | High-risk HER2+ early breast cancer (post-neoadjuvant) | EU, CN |
Enhertu | DESTINY-PanTumor02 | HER2+ solid tumours | CN |
Etcamah | SERENA-6 | ESR1m HR+ HER2- 1L advanced breast cancer | US |
Imfinzi | POTOMAC | NMIBC | JP |
Breztri | KALOS / LOGOS | Asthma | EU, JP |
Klygefa (gefurulimab) | PREVAIL | Generalised myasthenia gravis | JP |
Amlypave (anselamimab) | CARES | Kappa light chain amyloidosis | JP |
Ultomiris | I CAN | IgAN | US |
Ultomiris | ALXN1210-PNH-323 | PNH | CN |
Regulatory submissions or acceptances* in major regions
Medicine | Trial | Indication | Region |
Calquence | AMPLIFY | 1L CLL (fixed duration) | CN |
Imfinzi | VOLGA | MIBC not candidates for cisplatin | US, EU, JP |
Truqap | CAPItello-281 | PTEN-deficient mHSPC | CN |
tozorakimab | OBERON / TITANIA / PROSPERO | COPD | US, JP |
Ultomiris | I CAN | IgAN | CN |
Ultomiris | ALXN1210-TMA-314 | HSCT-TMA (paediatric) | US |
efzimfotase alfa | MULBERRY / CHESTNUT / HICKORY | HPP | US, EU, CN |
* US, EU and | |||
Other pipeline updates
For recent trial starts and anticipated timings of key trial readouts, please refer to the Clinical Trials Appendix document in the financial results section of the
Table 2: Key elements of financial performance: Q3 2026
For the quarter | Reported | Change | Core | Change |
| ||
ended 30 September | $m | Act | CER | $m | Act | CER |
|
Product Revenue | 16,173 | 7 | 7 | 16,173 | 7 | 7 | * See Tables 3, 7, 23, 24 and 25 for further details of Product Revenue, Product Sales and Alliance Revenue |
Collaboration Revenue | 36 | >3x | >3x | 36 | >3x | >3x | * See Tables 4 and 26 for further details of Collaboration Revenue |
Total Revenue | 16,209 | 7 | 7 | 16,209 | 7 | 7 | * See Tables 5 and 6 for Total Revenue by Therapy Area and by region |
Gross Margin (%) | 82 | - | +1pp | 82 | - | +1pp | + Positive product mix effects - Pricing headwinds, including those driven by loss of exclusivity and VBP in * Variations in Gross Margin can be expected between periods due to various factors, including fluctuations in foreign exchange rates, product seasonality and Collaboration Revenue |
R&D expense | 3,894 | 6 | 7 | 3,645 | 3 | 3 | * Core R&D: 22% of Total Revenue (23% for 9M 2026) + Increasing number of trials, and patients in those trials + Investments in transformative technologies + Addition of R&D projects from business development + Positive data readouts for high value pipeline opportunities that have ungated large late-stage trials * Variations in the year-on-year change in R&D expenses can be expected between periods due to the phasing of trial starts and completions |
SG&A expense | 5,108 | - | - | 3,909 | 2 | 2 | * Core SG&A: 24% of Total Revenue (25% for 9M 2026) + Investment to support ongoing and future launches * Variations in the year-on-year change in SG&A expenses can be expected between periods due to the phasing of product launches and other programmes |
Other operating income and expense4 | 277 | >3x | >3x | 277 | >2x | >2x | + Various partner milestones and royalties + Disposal of Zoryve interest |
Operating profit | 4,387 | 22 | 26 | 5,855 | 17 | 20 | + See commentary above on Gross Margin, R&D, SG&A and Other operating income and expense |
Operating Margin (%) | 27 | +3pp | +4pp | 36 | +3pp | +4pp | |
Net finance expense | 410 | 17 | 22 | 371 | 22 | 27 | + Lower interest income on short-term deposits and higher interest expense on short-term borrowings + Higher discount unwind on lease liabilities, principally due to the new strategic R&D centre in - Reported Net finance expense benefitted from a lower discount unwind on contingent consideration liabilities |
Tax rate (%) | 21 | -1pp | -1pp | 21 | - | -1pp | * Variations in the tax rate can be expected between periods |
EPS ($) | 2.02 | 23 | 26 | 2.79 | 17 | 19 | + See commentary above |
| |||||||
For dollar values in this table, the unit of change is percent. For Gross Margin, Operating Margin and Tax rate, the unit of change is percentage points (pp). | |||||||
| |||||||
In the table above, R&D expense, SG&A expense and Net finance expense are displayed as positive numbers. The plus and minus symbols next to comments denote the directional impact of the item being discussed. For example, a plus symbol next to a comment about an R&D item indicates that the item increased R&D expenditure relative to the prior year period. | |||||||
Corporate and business development
Summit Therapeutics
In October AstraZeneca completed a
Kendall Square R&D Centre
In October,
Reshaping for Sustainable Growth
insitro
In October,
Under the terms of the agreement, insitro will receive an upfront payment of
Dizal Pharmaceutical Co
In August,
Sustainability highlights
Reporting calendar
The Company intends to publish its FY and Q4 2026 results on
Conference call
A conference call and webcast for investors and analysts will begin today,
Notes
- Constant exchange rates. The differences between Actual Change and CER Change are due to foreign exchange movements between periods in 2026 vs. 2025. CER financial measures are not accounted for according to generally accepted accounting principles (GAAP) because they remove the effects of currency movements from Reported results.
- Core financial measures are adjusted to exclude certain items. The differences between Reported and Core measures are primarily due to costs relating to the amortisation of intangibles, impairments, legal settlements and restructuring charges. A full reconciliation between Reported EPS and Core EPS is provided in Tables 10 and 11 in the Financial Performance section of this document.
- 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.
- Income from disposals of assets and businesses, where the Group does not retain a significant ongoing economic interest, is recorded in Other operating income and expense in the Group’s financial statements.
To read AstraZeneca's 9M & Q3 2026 Financial Results press release in full, read here.
View source version on businesswire.com: https://www.businesswire.com/news/home/20261029477587/en/
Global Media Relations team
global-mediateam@astrazeneca.com
+44 (0)1223 344 800
Source: AstraZeneca