#1B AstraZeneca J.P. Morgan 41st Annual Healthcare Conference Aradhana Sarin Executive Director and Chief Financial Officer 9 January 2023#2Forward-looking statements 2 AstraZeneca (hereafter 'the Group') provides the following cautionary statement: this document contains certain forward-looking statements with respect to the operations, performance and financial condition of the Group, including, among other things, statements about expected revenues, margins, earnings per share or other financial or other measures. Although the Group believes its expectations are based on reasonable assumptions, any forward-looking statements, by their very nature, involve risks and uncertainties and may be influenced by factors that could cause actual outcomes and results to be materially different from those predicted. The forward-looking statements reflect knowledge and information available at the date of preparation of this document and the Group undertakes no obligation to update these forward-looking statements. The Group identifies the forward-looking statements by using the words 'anticipates', 'believes', 'expects', 'intends' and similar expressions in such statements. Important factors that could cause actual results to differ materially from those contained in forward-looking statements, certain of which are beyond the Group's control, include, among other things: ability of the Group and CinCor to complete the transactions contemplated by the acquisition agreement, including the parties' ability to satisfy the conditions to the consummation of the offer contemplated thereby and the other conditions set forth in the merger agreement; statements about the expected timetable for completing the transaction; the Group's and CinCor's beliefs and expectations and statements about the benefits sought to be achieved in the Group's proposed acquisition of CinCor; the potential effects of the acquisition on both the Group and CinCor; the possibility of any termination of the acquisition agreement; the expected benefits and success of baxdrostat and any combination product, the possibility that the milestone related to the contingent value right will not be achieved; the risk of failure or delay in delivery of pipeline or launch of new medicines; the risk of failure to meet regulatory or ethical requirements for medicine development or approval; the risk of failure to obtain, defend and enforce effective IP protection and IP challenges by third parties; the impact of competitive pressures including expiry or loss of IP rights, and generic competition; the impact of price controls and reductions; the impact of economic, regulatory and political pressures; the impact of uncertainty and volatility in relation to the UK's exit from the EU; the risk of failures or delays in the quality or execution of the Group's commercial strategies; the risk of failure to maintain supply of compliant, quality medicines; the risk of illegal trade in the Group's medicines; the impact of reliance on third- party goods and services; the risk of failure in information technology, data protection or cybercrime; the risk of failure of critical processes; any expected gains from productivity initiatives are uncertain; the risk of failure to attract, develop, engage and retain a diverse, talented and capable workforce; the risk of failure to adhere to applicable laws, rules and regulations; the risk of the safety and efficacy of marketed medicines being questioned; the risk of adverse outcome of litigation and/or governmental investigations; the risk of failure to adhere to increasingly stringent anti-bribery and anti-corruption legislation; the risk of failure to achieve strategic plans or meet targets or expectations; the risk of failure in financial control or the occurrence of fraud; the risk of unexpected deterioration in the Group's financial position; and the impact that global and/or geopolitical events such as the COVID-19 pandemic and the Russia-Ukraine war, may have or continue to have on these risks, on the Group's ability to continue to mitigate these risks, and on the Group's operations, financial results or financial condition. Nothing in this document, or any related presentation/webcast, should be construed as a profit forecast. There can be no guarantees that the conditions to the closing of the proposed transaction with CinCor will be satisfied on the expected timetable or at all or that baxdrostat or any combination product will receive the necessary regulatory approvals or prove to be commercially successful if approved.#3Science-led, patient-centered Developing innovative medicines for millions globally Science and innovation led 179 projects in our pipeline >35 major regulatory registrations events in 2022 13 new molecular entities in pipeline Diverse therapy area focus Oncology BioPharmaceuticals ● Cardiovascular, Renal & Metabolism (CVRM) ● Respiratory & Immunology (R&I) • Vaccines & Immune Therapies (V&I) Rare Disease Strength across primary, specialty and rare $33.1bn Total Revenue in 9M 2022 $5.28 Core EPS in 9M 2022 Committed to people, planet and society Environmental protection Scope 1 & 2: 98% reduction by 2026 Scope 3: 50% reduction by 2030¹ and 90% reduction by 2045 Access to healthcare to reach 50 million people² by 2025 Ethics and transparency with ambition of gender equality by 2025 1. Ambition Zero Carbon: to be carbon neutral across our global operations and fleet (Scope 1 and 2) by 2025 and carbon negative across our entire value chain by 2030, including offsets. Our net zero scope 1-3 science-based targets have been verified under the Science Based Targets initiative Net-Zero Corporate Standard: reducing our greenhouse gas emissions, Scope 1 and Scope 2, by 98% by early 2026, from 2015 baseline and reducing our 3 greenhouse gas emissions across Scope 3 by 50% by 2030, a 90% reduction by 2045, from 2019 baseline. 2. 50m people cumulatively reached through our flagship programmes: Healthy Heart Africa, Young Health Programme and Healthy Lung. B#4Entrepreneurial culture, focused on helping the world 4 LAAB = long-acting antibody. Our people and values We follow the science We put patients first We play to win We do the right thing We are entrepreneurial 83,000 employees worldwide 130 countries in which we operate Culture case study: our response to the COVID-19 pandemic test kit Drop of your We continued our clinical trials around the world and delivered medicines to patients We partnered with Oxford University to develop a vaccine made for the world at no profit during the pandemic Vaxzevria. COVID-19 Vaccine (ChAdOx1-S [recombinant]) We kept our employees safe through testing and bolstered the UK's national testing effort We mobilised our own research to advance the development of a LAAB, recognising that not everyone could receive a vaccine EVUSHELD tixagevimab, cilgavimab#5Strong financials Double digit growth in Oncology, BioPharmaceuticals and Rare Disease driving earnings growth and cash generation $24.4bn FY 2019 Total Revenue $26.6bn FY 2020 $37.4bn FY 2021 $33.1bn 9M 2022 +37% Growth¹ in 9M 2022 5 1. Growth rates for Total Revenue and Core EPS are at constant exchange rate. EPS = earnings per share. $3.50 FY 2019 Core EPS $4.02 FY 2020 $5.29 FY 2021 $5.28 9M 2022 +52% Growth¹ in 9M 2022 Net Cash Flow From Operating Activities $3.0bn FY 2019 $4.8bn FY 2020 $6.0bn FY 2021 $7.4bn 9M 2022 +16% Growth in 9M 2022#6Capital allocation priorities Effective deployment of capital to ensure opportunities for further growth S&P Global A A-2 Stable Long term: Short term: Outlook: Acquisitions Strong investment grade rating CINCOR ALEXION AstraZeneca Rare Disease THERAPEUTICS neo gene THERAPEUTICS TeneoTwo Inc Value-adding business development Collaborations Daiichi-Sankyo CAELUM BIOSCIENCES AMGEN IONIS GRAIL MOODY'S Long term: Short term: Outlook: mind MERCK AG sanofi ROBIO C 4 X D SCORPION A3 P-2 Stable "T'EMPUS In-licensing UNIVERSITY OF OXFORD VANDERBILT UNIVERSITY HARBOUR BIOMED neurimmune Reinvestment in the business R&D spend: low twenties percentage of Total Revenue¹ Late-stage development Discovery Medical Affairs and other Returning value Early-stage development 6 1. Core R&D Expense as a percentage of Total Revenue was 21.5% in 9M 2022. 2. Progressive dividend policy defined as dividend per share either stable or increasing in US dollar terms. R&D = Research & Development. illustrative split of R&D investment Progressive dividend policy² 3#7Strengthening scientific leadership Extensive R&D investment in cutting-edge platforms and technology 'Growth Through Innovation' investing in four areas to create the greatest and swiftest impact on disease ● ● ● ● ● Small molecules PROTACS Nanoparticles Epigenetics Cell-based therapeutics CAR-T therapy Macrophage therapy TReg stabilisation ● ● ● ● ● ● Enhancing our understanding of disease biology Antibody therapeutics Monoclonal ADCs Bispecifics ● ● Better predictions of clinical success Fragments T-cell engagers Peptide/protein therapeutics Therapeutic proteins Bicyclic peptides Anticalin proteins Pioneering new approaches to clinical interventions ● Nucleotide-based therapeutics Antisense oligonucleotides Oligonucleotide conjugates Therapeutic gene editing siRNA mRNA Creating the next generation of therapeutics ● Underpinned by advancements in Data, Al and Digital Health > in vivo-expressed biologics Viral vectors DNA vectors 7 PROTACS = proteolysis targeting chimeras; ADCs = antibody-drug conjugates; CAR-T = chimeric antigen receptor (CAR) T-cell therapy; Treg = regulatory T-cell; siRNA = small interfering ribonucleic acid; mRNA = modified ribonucleic acid; DNA = deoxyribonucleic acid; Al = artificial intelligence. B#8Continuing momentum in commercial execution across all therapy areas, into new diseases and geographies 9M 2022 2023 focus TAGRISSOⓇ IMFINZIⓇ osimertinib CALQUENCE (acalabrutinib) 100 mg capsules ENHERTUⓇ fam-trastuzumab deruxtecan-nxki 20 mg/mL INJECTION FOR INTRAVENOUS USE durvalumab Injection for Intravenous Use 50 mg/ml blockbusters with double digit growth IMFINZIⓇ durvalumab CIMJUDOⓇ tremelimumab-actl winning in Gl cancer Oncology TR: 24% GROWTH (CER) DENHERTU' tam-trastuzumab deruxtecan-nxki 20 mg/mL INJECTION FOR INTRAVENOUS USE redefining breast cancer Lynparza olaparib 77% growth 9M 2022 165% growth 9M 2022 TAGRISSO osimertinib expanding in adjuvant Lynparza olaparib s tablets 150 mg expanding into 1L mCRPC CALQUENCE (acalabrutinib) 100 mg capsules consolidating leadership in CLL BioPharmaceuticals TR: 16% GROWTH (CER) 90 farxiga fastest growing SGLT2i globally three consecutive blockbuster quarters in 2022 BREZTRI TEZSPIREⓇ (tezepelumab-ekko) injection 210 mg accelerating recent launches Beyfortus approved in the EU for RSV 9.0 farxiga expanding into HFpEF Saphnelo (anifrolumab-fnia) Intravenous Use 300 mg/vial PT027 launch/access prep Rare Disease TR: 10% GROWTH (CER)* SOLIRISⓇ (eculizumab) Injection for Intravenous Use 300 mg/30 mL vial aHUS and PNH launch in China ULTOMIRIS® (ravulizumab-cwvZ) injection for intravenous use 300 mg/3 mL vial growth in gMG and NMOSD¹ *Proforma growth. 1. Ultomiris NMOSD regulatory decision anticipated in H1 2023 in US and EU. GI = gastrointestinal; CLL = chronic lymphocytic leukaemia; SGLT2i = sodium-glucose co-transporter-2 inhibitor; aHUS = atypical 8 haemolytic uraemic syndrome; PNH = paroxysmal nocturnal haemoglobinuria; gMG = generalised myasthenia gravis; NMOSD = neuromyelitis optica spectrum disorder. Collaboration partners: Merck (Lynparza), Daiichi Sankyo (Enhertu), Sanofi (Beyfortus), Amgen (Teszpire), Avillion (PT027). ULTOMIRISⓇ (ravulizumab-cwvVZ) injection for intravenous use 300 mg/3 mL vial 35% growth 9M 2022 following gMG approval Strensio (asfotase alfa) for injection continued demand momentum 3#9AstraZeneca positioned to lead in CVRM AstraZeneca to acquire CinCor Pharma to strengthen cardiorenal pipeline Enhancing our position in CVRM Developing and delivering innovative, life-changing medicines and solutions for the millions of people affected by the complex spectrum of CVRM diseases Dyslipidaemia /Thrombosis ↓ Andexxa AZD0870 y Heart failure Farxiga mitiperstat balcinrenone G Chronic kidney disease ↓ Farxiga mitiperstat balcinrenone zibotentan Transthyretin amyloidosis ↓ eplontersen Metabolism ↓ zibotentan Early pipeline Hypertension ↓ baxdrostat CINCOR baxdrostat CINCOR Improving treatment and outcomes for patients; building on Farxiga's success 9 BP = blood pressure; ASIS = aldosterone synthase inhibitors; MRAs = mineralocorticoid receptor antagonists. Collaboration partner: Ionis (eplontersen). The clinical burden of treatment resistant hypertension Hypertension, a silent killer: systolic blood pressure above 130/80 mm Hg 7 million patients in the US are on three or more anti- hypertensive medicines and are still not at BP goal - treatment resistant Current standard of care: ASIS and MRAS (spironolactone) target the aldosterone pathway to lower BP MRAS → undesirable androgenic side effects e.g., gynecomastia#10Baxdrostat: addresses a large unmet need in cardiorenal disease A potential best-in-class ASI for treatment resistant hypertension Baxdrostat (CIN-107) – a highly selective, aldosterone synthase inhibitor (ASI) Baxdrostat is highly selective for aldosterone synthase and spares the cortisol pathway BrigHTN Phase II trial: Baxdrostat significantly reduced systolic BP after 12-week treatment period, in treatment-resistant hypertensive patients (on diuretics, CCBS, BBs, ACES or ARBs) C Change in Systolic Blood Pressure over Time -Placebo - Baxdrostat, →→ Baxdrostat, 0.5 mg 1 mg LSM Change (mm Hg) 0- -5- -10- -15- -20- -25- -30+ 0 20 40 T 60 →Baxdrostat, 2 mg 80 100 Trial Day Well tolerated in Phase II trials, does not generate the same level of androgenic AEs as MRAs used for trHTN Hypertension: high-risk factor for stroke, CAD, heart attack and CKD; current treatment options limited Baxdrostat is a potential leading next-generation ASI: expected to help control blood pressure in patients with tough to control hypertension. Phase III to start H1 2023 Strong strategic fit to build leading cardiorenal portfolio: potential for combinations with Farxiga, aiming to provide both BP reduction and organ protection Deal terms $26 per share in cash at deal closing (upfront equity value of $1.3bn) - At transaction close, AstraZeneca will acquire CinCor's cash and marketable securities (~$0.5bn) A non-tradable contingent value right of $10 per share in cash payable upon a specified regulatory submission of baxdrostat 10 CCB = calcium channel blockers; BBs = beta blockers; ACE = angiotensin-converting enzyme; AE = adverse events; ARBS = angiotensin receptor blockers; ASI = aldosterone synthase inhibitors; MRAS = mineralocorticoid receptor antagonists; CAD = coronary arterial disease; CKD = chronic kidney disease; BP = blood pressure; trHTN = treatment-resistant hypertension.#1111 2022: An incredible year of clinical success Exceptional delivery of best-in-industry pipeline Positive Phase III data readouts, selected Enhertu DESTINY-Breast04 HER2-low breast cancer eplontersen - NEURO-TTRansform ATTRv-PN Lynparza - OlympiA early breast cancer (US, EU, JP) Regulatory approvals in major markets, including: Ultomiris - CHAMPION-MG gMG (US, EU, JP) Enhertu - DESTINY-Breast04 HER2-low breast cancer (US) Beyfortus - MELODY/MEDLEY RSV (EU) Tezspire - NAVIGATOR severe asthma (EU, JP) Ultomiris - CHAMPION-NMOSD neuromyelitis optica spectrum disorder Imfinzi/Imjudo - HIMALAYA unresectable liver cancer (US, JP) danicopan - ALPHA PNH with clinically significant EVH Lynparza - PROpel metastatic CRPC (EU) Evusheld-PROVENT/TACKLE COVID-19 prevention/treatment (EU, JP) Enhertu - DESTINY-Breast03 HER2-positive breast cancer (US, EU) Enhertu - DESTINY-Lung02 HER2-low breast cancer (US) Imfinzi - TOPAZ-1 biliary tract cancer (US, EU, JP) Lynparza - PAOLA-1 HRD-positive ovarian cancer (CN) Soliris - PNH and aHUS (CN) Farxiga - DELIVER HFpEF Imfinzi - POSEIDON NSCLC (JP) capivasertib - CAPItello-291 advanced breast cancer Ondexxya - ANNEXA-4 acute major bleeds (JP) Saphnelo - MUSE/TULIP1&2 lupus (EU) Enhertu - DESTINY-Gastric01/02 gastric cancer (EU) Calquence ELEVATE-TN CLL (JP) HER2-low = human epidermal growth factor receptor 2-low; NMOSD neuromyelitis optica spectrum disorder; HFpEF = heart failure with preserved ejection faction; ATTRv-PN = hereditary transthyretin-mediated amyloid polyneuropathy; PNH = paroxysmal nocturnal haemoglobinuria; EVH = extravascular haemolysis; gMG = generalised yasthenia gravis; HER2-positive = human epidermal growth factor receptor 2-positive; EGFRm = epidermal growth factor receptor mutated; RSV = respiratory syncytial virus; HRD-positive = homologous recombination deficiency-positive; NF1 = neurofibromatos type 1; PN = plexiform neurofibromas; aHUS = atypical haemolytic uraemic syndrome; CRPC = castrate-resistant cancer; chronic lymphocytic leukaemia; CLL = chronic lymphocytic leukaemia. Collaboration partners: Merck (Lynparza, Koselugo), Daiichi Sankyo (Enhetu), Sanofi (Beyfortus), Amgen (Teszpire). Tagrisso - ADAURA early EGFRm lung cancer (JP) Forxiga - DAPA-CKD chronic kidney disease (CN) Koselugo - SPRINT NF1-PN (JP)#12Key upcoming newsflow and selected next wave pipeline 12 sta Regulatory decision Key Phase III data readouts H1 2023 Imfinzi - biliary tract cancer (TOPAZ-1) (EU) Imfinzi - liver cancer (1L) (HIMALAYA) (EU) Enhertu - HER2-low breast cancer (3L) (DESTINY-Breast04) (EU) Enhertu - HER2+ gastric cancer (2L) (DESTINY-Gastric01) (EU) Enhertu - HER2+ breast cancer (2L) (DESTINY-Breast03) (CN) Enhertu - HER2-low breast cancer (3L) (DESTINY-Breast04) (JP, CN) Farxiga - HFpEF (DELIVER) PT027-asthma (MANDALA/DENALI) (US) Ultomiris - NMOSD (CHAMPION-NMOSD) Tagrisso - EGFRm NSCLC (1L) (FLAURA2) Imfinzi - SCLC (limited-stage) (ADRIATIC) Imfinzi - NSCLC (neoadjuvant) (AEGEAN) Imfinzi - liver cancer (adjuvant) (EMERALD-2) Lynparza - ovarian cancer (1L) (DUO-O) Dato-DXd - NSCLC (3L) (TROPION-Lung01) roxadustat - anaemia of myelodysplastic syndrome Oncology BioPharmaceuticals Rare Disease H2 2023 Beyfortus - RSV (US) Soliris-gMG (CN) Koselugo - NF1-PN (SPRINT) (CN) Tagrisso - EGFRm NSCLC (unresectable Stg. III) (LAURA) Imfinzi - NSCLC (unresectable, Stg. III) (PACIFIC-2) Imfinzi- bladder cancer (muscle invasive) (NIAGARA) Imfinzi - bladder cancer (1L) (NILE) Lynparza - endometrial cancer (1L) (DUO-E) Enhertu - HER2-low breast cancer (2L) (DESTINY-Breast06) Calquence - MCL (1L) (ECHO) capivasertib-TNBC (locally adv./met.) (CAPItello-290) Farxiga - myocardial infarction (DAPA-MI) Fasenra - EGPA (MANDARA) Fasenra-HES (NATRON) Next wave early pipeline AZD8205 - B7H4 Top1i ADC AZD0486-CD3xCD20 TCE AZD9592 - EGFR/CMET Top1i ADC volrustomig - PD1/CTLA4 bispecific AZD5851 GPC3 armoured CAR-T AZD2693- PNPLA3 AZD3427 - relaxin AZD0780oPCSK9 AZD6793 - IRAK4 AZD8630 - ITSLP vemircopan - oral Factor D gefurulimab - C5 mini-body ALXN1850 - ng asfotase alfa ALXN1820-anti-properdin 1L = 1st-line; 2L = 2nd-line; 3L = 3rd-line; HER2-low = human epidermal growth factor receptor 2-low; HER2+ = human epidermal growth factor receptor 2-positive; HFpEF = heart failure with preserved ejection faction; NMOSD = neuromyelitis optica spectrum disorder; EGFRm = epidermal growth factor receptor mutated; SCLC = small cell lung cancer; NSCLC = non-small cell lung cancer; Dato-DXd = datopotamab deruxtecan; RSV = respiratory syncytial virus; gMG = generalised myasthenia gravis; NF1= neurofibromatosis type 1; PN = plexiform neurofibromas; MCL = mantle cell lymphoma; TNBC = triple negative breast cancer; EGPA = eosinophilic granulomatosis with polyangiitis; HES = hyper eosinophilic syndrome; ADC = antibody-drug conjugate; TCE = T-cell engager; PD1 = programmed cell death protein 1; CTLA4 = cytotoxic T-lymphocyte associated protein 4; CAR-T = chimeric antigen receptor (CAR) T- cell therapy; PNPLA3 = patatin-like phospholipase domain-containing protein 3; PCSK9 = proprotein convertase subtilisin/kexin type 9; IRAK4 = interleukin-1 receptor-associated kinase 4; iTSLP = inhaled thymic stromal lymphopoietin; ng = next-generation. Collaboration partners: Merck (Lynparza), Daiichi Sankyo (Enhertu, Dato-DXd), Sanofi (Beyfortus), Amgen (Teszpire), Avillion (PT027).#13AstraZeneca: positioned to deliver industry-leading growth Optimised LoE profile Mid- and long-term durability Ultom iris Dato-Dxd En hertu Tagrisso Calquence Imfinzi Lynparza Soliris Farxiga Brilinta 2020 2025 2030 Growth from robust portfolio and an innovative pipeline All growth rates at CER¹ Low twenties % increase in 2022 1 2021 2022 2021-2025 low double digit CAGR² 2025 Total Revenue from COVID-19 medicines in 2021 and 2022 Industry-leading growth post 2025 Managed LOE • Diversified portfolio • Transition to next generation medicines 13 1. Constant Exchange Rates. 2. CAGR = compound annual growth rate. Double-digit CAGR of non-COVID-19 Total Revenue from 2021 (Alexion proforma) to 2025, assuming Constant Exchange Rates. Pipeline • Indication expansion Geographic expansion • Future launches of NMES with validated mechanisms Bar charts are illustrative only, not to scale B#14AstraZeneca: a sustainable, long-term growth opportunity Multiple organic levers drive momentum and sustain attractive growth profile 14 CAGR = compound annual growth rate. 1 Industry-leading execution 2 3 Strong track-record across key therapy areas Late-stage pipeline success Robust breadth and depth of Phase II and Phase III programmes including several high potential medicines Investment in early-stage Advancing key assets with blockbuster-potential and investing in new platforms and technology to unlock the next waves of growth Committed to delivering Low double-digit revenue CAGR through 2025 AND industry-leading growth 2025+ B#1515 Closing comments and Q&A M#1616 Investor Relations Andy Barnett Head of Investor Relations [email protected] Morgan Sanford Oncology [email protected] Philip Sparks BioPharmaceuticals (R&I, V&I), Other medicines [email protected] Rachel Korolyshun Rare Disease, ESG [email protected] Josie Afolabi Oncology [email protected] Christer Gruvris BioPhamaceuticals (CVRM), Finance and Fixed Income [email protected] Lauren Swales Rare Disease, ESG [email protected] B#17Important information about the tender offer 17 The tender offer described in this presentation has not yet commenced. This presentation is for informational purposes only and is neither an offer to purchase nor a solicitation of an offer to sell any shares of the common stock of CinCor or any other securities, nor is it a substitute for the tender offer materials described herein. At the time the planned tender offer is commenced, a tender offer statement on Schedule TO, including an offer to purchase, a letter of transmittal and related documents, will be filed by AstraZeneca PLC (AstraZeneca), AstraZeneca Finance and Holdings Inc. and Cinnamon Acquisition, Inc., a wholly-owned indirect subsidiary of AstraZeneca, with the Securities and Exchange Commission (the SEC), and a solicitation/recommendation statement on Schedule 14D-9 will be filed by CinCor with the SEC. INVESTORS AND SECURITY HOLDERS ARE URGED TO CAREFULLY READ BOTH THE TENDER OFFER MATERIALS (INCLUDING AN OFFER TO PURCHASE, A RELATED LETTER OF TRANSMITTAL AND CERTAIN OTHER TENDER OFFER DOCUMENTS) AND THE SOLICITATION/RECOMMENDATION STATEMENT ON SCHEDULE 14D-9 REGARDING THE OFFER, AS THEY MAY BE AMENDED FROM TIME TO TIME, WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION THAT INVESTORS AND SECURITY HOLDERS SHOULD CONSIDER BEFORE MAKING ANY DECISION REGARDING TENDERING THEIR SECURITIES. Investors and security holders may obtain a free copy of the Offer to Purchase, the related Letter of Transmittal, certain other tender offer documents and the Solicitation/Recommendation Statement (when available) and other documents filed with the SEC at the website maintained by the SEC at www.sec.gov or by directing such requests to the information agent for the tender offer, which will be named in the tender offer statement. In addition, CinCor files annual, quarterly and current reports and other information, and AstraZeneca files annual reports and other information with the SEC, which are available to the public from commercial document-retrieval services and at the SEC's website at www.sec.gov. Copies of the documents filed with the SEC by AstraZeneca may be obtained at no charge on AstraZeneca's internet website at www.astrazeneca.com/investors. Copies of the documents filed with the SEC by CinCor may be obtained at no charge under the "Investors" section of CinCor's internet website at www.cincor.com. B#1818 Confidentiality Notice This file is private and may contain confidential and proprietary information. If you have received this file in error, please notify us and remove it from your system and note that you must not copy, distribute or take any action in reliance on it. Any unauthorized use or disclosure of the contents of this file is not permitted and may be unlawful. AstraZeneca PLC, 1 Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge, CB2 OAA, UK, T: +44(0)203 749 5000, www.astrazeneca.com B