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    AstraZeneca Full year and Q4 2023 Financial Results

    2/8/24 2:03:00 AM ET
    $AZN
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Get the next $AZN alert in real time by email

    Strong growth and pipeline momentum with three new medicines approved since the third quarter

    AstraZeneca:

    Revenue and EPS summary

     

     

    FY 2023

    Q4 2023

     

     

     

    % Change

     

    % Change

    $m

    Actual

     

    CER1

     

    $m

    Actual

    CER

    - Product Sales

    43,789

    2

     

    4

     

    11,323

    5

    5

    - Alliance Revenue2

     

    1,428

    89

     

    89

     

    424

    69

    67

    - Collaboration Revenue2

    594

    (1

    )

    (1

    )

    277

    75

    74

    Total Revenue

     

    45,811

    3

     

    6

     

    12,024

    7

    8

    Total Revenue ex COVID-19

     

    45,488

    13

     

    15

     

    12,036

    16

    16

    Reported EPS

    $3.84

    81

     

    96

     

    $0.62

    7

    5

    Core3 EPS

    $7.26

    9

     

    15

     

    $1.45

    5

    7

    Financial performance for full year 2023 (Growth numbers at CER)

    • Total Revenue $45,811m, up 6% despite a decline of $3,736m from COVID-19 medicines4
    • Excluding COVID-19 medicines, Total Revenue increased 15% and Product Sales increased 14%
    • Double-digit Total Revenue growth from Oncology 21%, CVRM 18%, R&I 10%, and Rare Disease 12%
    • Core Product Sales Gross Margin5 of 82%, up two percentage points, reflecting the decline in sales of lower margin COVID‑19 medicines
    • Core Operating Margin of 32% increased by two percentage points including the previously announced gain from an update to the contractual relationships for Beyfortus, totalling $712m and recorded as Core Other operating income. In the quarter, higher SG&A expense drove lower operating margins, partly due to phasing of expenses and increased investment in launches for Airsupra, Wainua and Truqap
    • The Core Tax Rate for the year was 17%. In the fourth quarter, the tax rate was negatively impacted by reviews by tax authorities, administrative appeal processes and other adjustments, offset by a routine intragroup reorganisation of IP, leading to a tax rate of 10% in the quarter
    • Core EPS increased 15% to $7.26
    • Second interim dividend declared of $1.97 per share, making a total dividend declared for FY 2023 of $2.90 per share
    • Total Revenue and Core EPS in FY 2024 are each expected to increase by a low double-digit to low teens percentage at CER

    Pascal Soriot, Chief Executive Officer, AstraZeneca, said:

    "As AstraZeneca celebrates its 25th anniversary, we are pleased to report another year of strong financial performance and scientific progress, with double-digit earnings growth, and investment in exciting areas of science, including antibody drug conjugates and cell therapies, that lay the foundations for long-term success.

    We expect another year of strong growth in 2024, driven by continued adoption of our medicines across geographies. Our differentiated and growing portfolio of approved medicines, global reach and rich R&D pipeline give us confidence that we will continue to deliver industry-leading growth."

    Key milestones achieved since the prior results announcement

    • Three first approvals for new molecular entities: Truqap (capivasertib), Wainua (eplontersen), Voydeya (danicopan)
    • US approvals for Truqap plus Faslodex in HR-positive, HER2-negative advanced breast cancer with biomarker alterations (CAPItello-291), and Wainua for ATTRv-PN (NEURO-TTRansform). China approvals for Imfinzi in mBTC (TOPAZ-1) and Beyfortus for prevention of RSV in infants (MEDLEY/MELODY). First approval, in Japan, for Voydeya, as an add-on therapy to Ultomiris or Soliris for PNH with EVH (ALPHA)
    • Enhertu granted Priority Review in the US for patients with metastatic HER2-positive solid tumours

    Guidance

    The Company issues its Total Revenue and Core EPS guidance for FY 2024 at CER, based on the average foreign exchange rates through 2023.

     

    Total Revenue is expected to increase by a low double-digit to low teens percentage

    Core EPS is expected to increase by a low double-digit to low teens percentage

     
    • Collaboration Revenue is expected to increase substantially, driven by success-based milestones and certain anticipated transactions
    • Other operating income is expected to decrease substantially (FY 2023 included a $241m gain on the disposal of Pulmicort Flexhaler US rights, and a $712m one-time gain relating to updates to contractual arrangements for Beyfortus)
    • 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 2024 to December 2024 were to remain at the average rates seen in January 2024, it is anticipated that both FY 2024 Total Revenue and Core EPS would incur a low single-digit adverse impact versus the performance at CER. The Company's foreign exchange rate sensitivity analysis is provided in Table 19.

    Investor Day

    AstraZeneca will host an Investor Day on 21 May 2024.

    For more information, see www.astrazeneca.com/investor-relations.html.

    Table 1: Key elements of Total Revenue performance in Q4 2023

     

    % Change

    Revenue type

     

    $m

    Actual %

     

    CER %

     

     

     

    Product Sales

    11,323

    5

     

    5

     

     

    * Excluding COVID-19 medicines, Q4 2023 Product Sales increased by 14%

    Alliance Revenue

     

    424

    69

     

    67

     

     

    * $281m for Enhertu (Q4 2022: $188m)

    * $80m for Tezspire (Q4 2022: $37m)

    * $41m for Beyfortus (Q4 2022: $nil)

    Collaboration Revenue

    277

    75

     

    74

     

     

    * $245m Lynparza regulatory milestone (Q4 2022: $105m)

    * $27m Beyfortus sales milestone (Q4 2022: $nil)

    Total Revenue

     

    12,024

    7

     

    8

     

     

    * Excluding COVID-19 medicines, Q4 2023 Total Revenue increased by 16%

    Therapy areas

    $m

    Actual %

     

    CER %

     

     

     

    Oncology

    4,989

    23

     

    24

     

     

    * Strong performance across all key medicines and regions

    CVRM

    2,702

    18

     

    18

     

     

    * Farxiga up 36% (35% at CER), Lokelma up 38%, roxadustat up 27%, Brilinta declined 5% (4% at CER)

    R&I

     

    1,675

    13

     

    13

     

     

    * Fasenra up 10% (9% CER), Breztri up 72%. Saphnelo and Tezspire also continue to grow rapidly, partially offset by a 16% decline in Symbicort following entry of a generic competitor in the US in the third quarter

    V&I

     

    413

    (64

    )

    (66

    )

     

    * $6m revenue from COVID-19 mAbs and ‑$17m for Vaxzevria, both resulting from historic contracts (Q4 2022: $734m and $95m respectively)

    * Beyfortus $122m, including $41m of Alliance Revenue for AstraZeneca's share of gross profits outside US, $27m of Collaboration Revenue for a sales milestone and $54m of Product Sales from product supplied to Sanofi

    Rare Disease

     

    1,971

    9

     

    9

     

     

    * Ultomiris up 39% (38% at CER), partially offset by decline in Soliris of 15% (13% at CER)

    * Strensiq up 12% (13% at CER) and Koselugo up 46% (48% at CER) reflecting strong patient demand

    Other Medicines

     

    274

    (33

    )

    (32

    )

     

    * Nexium generic competition in Japan

    Total Revenue

     

    12,024

    7

     

    8

     

     

     

    Regions inc. COVID-19

     

    $m

    Actual %

     

    CER %

     

     

     

    US

    5,101

    7

     

    6

     

     

     

    Emerging Markets

     

    2,783

    2

     

    8

     

     

     

    - China

    1,382

    16

     

    16

     

     

     

    - Ex-China Emerging Markets

     

    1,401

    (9

    )

    2

     

     

     

    Europe

     

    2,880

    25

     

    17

     

     

     

    Established RoW

     

    1,259

    (9

    )

    (6

    )

     

     

    Total Revenue inc. COVID-19

     

    12,024

    7

     

    8

     

     

    * Growth rates impacted by lower sales of COVID-19 medicines (see table below)

    Regions ex. COVID-19

     

    $m

    Actual %

     

    CER %

     

     

    US

     

    5,101

    12

     

    12

     

     

     

    Emerging Markets

     

    2,791

    15

     

    22

     

     

     

    - China

     

    1,382

    16

     

    16

     

     

     

    - Ex-China Emerging Markets

     

    1,409

    14

     

    27

     

     

     

    Europe

     

    2,884

    33

     

    25

     

     

     

    Established RoW

     

    1,259

    4

     

    8

     

     

     

    Total Revenue ex. COVID-19

     

    12,036

    16

     

    16

     

     

     

    Table 2: Key elements of financial performance in Q4 2023

    Metric

    Reported

    Reported

    change

    Core

    Core

    change

     

    Comments6

    Total Revenue

    $12,024m

    7% Actual

    8% CER

    $12,024m

    7% Actual

    8% CER

     

    * Excluding COVID-19 medicines, Q4 2023 Total Revenue increased by 16%

    * See Table 1 and the Total Revenue section of this document for further details

    Product Sales Gross Margin

    80%

    +6pp Actual

    +6pp CER

    80%

    +3pp Actual

    +2pp CER

     

    + In the prior year period, gross margins were reduced due to inventory write-downs and manufacturing contract terminations for Evusheld

    * Variations in Product Sales Gross Margin can be expected between periods due to product seasonality, foreign exchange fluctuations and other effects

    R&D expense

    $3,073m

    17% Actual

    15% CER

    $2,914m

    15% Actual

    14% CER

     

    + Increased investment in the pipeline

    * Core R&D-to-Total Revenue ratio of 24% (Q4 2022: 23%)

    + Quarterly phasing impact

    SG&A expense

    $5,371m

    16% Actual

    16% CER

    $4,034m

    13% Actual

    12% CER

     

    + Market development for recent launches and pre-launch activities

    * Core SG&A-to-Total Revenue ratio of 34% (Q4 2022: 32%)

    + Quarterly phasing impact

    Other operating income and expense7

    $107m

    -43% Actual

    -42% CER

    $107m

    -17% Actual

    -15% CER

     

    ‒ Discontinuation of brazikumab development

    Operating Margin

    10%

    +1pp Actual

    +1pp CER

    23%

    Stable

     

    * See Product Sales Gross Margin, expenses and Other operating income and expense commentary above

    Net finance expense

    $337m

    7% Actual

    3% CER

    $259m

    5% Actual

    1% CER

     

    + Higher rates on floating debt and bond issuances

    + Increased Interest expense on income tax balances

    ‒ Higher interest received on cash and short-term investments

    Tax rate

    -7%

    +9pp Actual

    +13pp CER

    10%

    Stable

     

    ‒ Intragroup purchase of intellectual property

    + Reviews by tax authorities, administrative appeals and changes to certain deferred tax balances

    * Variations in the tax rate can be expected between periods

    EPS

    $0.62

    7% Actual

    5% CER

    $1.45

    5% Actual

    7% CER

     

    * Further details of differences between Reported and Core are shown in Table 14

    Table 3: Pipeline highlights since prior results announcement

    Event

    Medicine

    Indication / Trial

    Event

    Regulatory approvals and other regulatory actions

    Truqap

    HR-positive HER2-negative advanced breast cancer with biomarker alterations (CAPItello-291)

    Regulatory approval (US)

     

    Imfinzi

    Biliary tract cancer (TOPAZ-1)

    Regulatory approval (CN)

     

    Wainua

    ATTRv-PN (NEURO-TTRansform)

    Regulatory approval (US)

     

    Beyfortus

    RSV (MELODY-MEDLEY)

    Regulatory approval (CN)

     

    Voydeya

    PNH with EVH (ALPHA)

    Regulatory approval (JP)

    Regulatory submissions or acceptances*

    Lynparza

    gBRCA breast cancer (adjuvant) (OlympiA)

    Regulatory submission (CN)

    Lynparza + Imfinzi

    Endometrial cancer (1st-line) (DUO-E)

    Regulatory submission (US, EU, JP)

    Enhertu

    HER2-expressing tumours (DESTINY-PanTumor02, DESTINY-Lung01, DESTINY-CRC02)

    Regulatory submission (US), Priority Review (US)

    Enhertu

    HER2+/HER2-low gastric (1st-line) (DESTINY-Gastric01)

    Regulatory submission (CN)

    Imfinzi + Imjudo

    NSCLC (neoadjuvant) (AEGEAN)

    Regulatory submission (EU)

    Wainua

    ATTRv-PN (NEURO-TTRansform)

    Regulatory submission (EU)

    Fasenra

    EGPA (MANDARA)

    Regulatory submission (US, EU, JP)

    Ultomiris

    NMOSD (CHAMPION-NMOSD)

    Regulatory submission (US)

    Ultomiris

    gMG

    Regulatory submission (CN)

    Major Phase III data readouts and other developments

    Imfinzi

    NSCLC (unresectable, Stg. III) (PACIFIC-2)

    Primary endpoint not met

     

    acoramidis 8

    ATTR-CM

    Primary endpoint met

    *US, EU and China regulatory submission denotes filing acceptance

    Upcoming pipeline catalysts

    For a table of anticipated timings of key trial readouts, please refer to page 3 of the Clinical Trials Appendix, available on www.astrazeneca.com/investor-relations.html.

    Table 4: Phase III trials started since 1 January 2023

    Medicine

    Trial name

    Indication

    datopotamab deruxtecan

    AVANZAR

    NSCLC (1st-line)

     

    TROPION-Lung07

    Non-squamous NSCLC (1st-line)

     

    TROPION-Breast04

    Neoadjuvant/adjuvant triple-negative or HR-low/HER2-negative breast cancer

     

    TROPION-Breast05

    PD-L1-positive locally recurrent inoperable or metastatic TNBC

    camizestrant

    CAMBRIA-1

    HR-positive/HER2-negative adjuvant breast cancer

     

    CAMBRIA-2

    HR-positive/HER2-negative adjuvant breast cancer

    Truqap

    CAPItello-292

    HR-positive/HER2-negative advanced breast cancer

    volrustomig

    eVOLVE-Cervical

    High-risk locally advanced cervical cancer

    eVOLVE-Lung02

    mNSCLC (1st-line) with PD-L1 <50%

     

    eVOLVE-Meso

    Unresectable malignant pleural mesothelioma (1st-line)

     

    eVOLVE-HNSCC

    Unresected, locally advanced HNSCC

    rilvegostomig

    ARTEMIDE-Biliary01

    BTC with curative intent

    saruparib

    EvoPAR-PR01

    HRRm and Non-HRRm mCSPC

    zibo/dapa

    ZENITH High Proteinuria

    CKD with high proteinuria

    Saphnelo

    DAISY

    Systemic sclerosis

    baxdrostat

    BaxHTN

    Uncontrolled, including treatment-resistant, hypertension

    Tezspire

    CROSSING

    Eosinophilic oesophagitis

    Breztri

    LITHOS

    Mild to moderate asthma

     

    ATHLOS

    COPD

    pMDI portfolio

    HFO1234ze + Breztri

    COPD

     

    HFO1234ze

    Mucociliary clearance in healthy volunteers

     

    HFO1234ze

    Asthma

    tozorakimab

    MIRANDA

    COPD

    ipavibart (AZD3152)

    SUPERNOVA

    COVID-19 prophylaxis

    Ultomiris

    ARTEMIS

    Cardiac surgery-associated acute kidney injury

    ALXN2220

    DepleTTR-CM

    Transthyretin amyloid cardiomyopathy

    efzimfotase alfa (ALXN1850)

    HICKORY

    Hypophosphatasia

    Corporate and business development

    In November 2023, AstraZeneca launched Evinova, with an ambition to become a leading provider of digital health solutions to better meet the needs of healthcare professionals, regulators and patients. Evinova will prioritise bringing to market established and scaled digital technology solutions already being used globally by AstraZeneca to optimise clinical trial design and delivery. Globally-leading clinical research organisations Parexel and Fortrea have entered into agreements to offer Evinova digital health solutions to their wide customer base.

    In December 2023, AstraZeneca entered into a definitive agreement to acquire Icosavax, Inc (Icosavax). The acquisition strengthens AstraZeneca's late-stage pipeline with Icosavax's lead investigational vaccine candidate, IVX-A12, a potential first-in-class, Phase III-ready, combination VLP vaccine that targets both RSV and hMPV. RSV and hMPV are both leading causes of severe respiratory infection and hospitalisation in adults 60 years of age and older and those with chronic conditions such as cardiovascular, renal and respiratory disease. Subject to the satisfaction of the conditions in the merger agreement, the acquisition is expected to close in the first quarter of 2024.

    In December 2023, AstraZeneca entered into a definitive agreement to acquire Gracell Biotechnologies Inc. (Gracell), a global clinical-stage biopharmaceutical company developing innovative cell therapies for the treatment of cancer and autoimmune diseases. The proposed acquisition will enrich AstraZeneca's growing pipeline of cell therapies with GC012F, a novel, clinical-stage FasTCAR-enabled BCMA and CD19 dual-targeting CAR-T therapy, a potential new treatment for multiple myeloma, as well as other haematologic malignancies and autoimmune diseases including systemic lupus erythematosus. The transaction is expected to close in the first quarter of 2024, subject to customary closing conditions, including regulatory clearances, and Gracell shareholder approval.

    In February 2024, AstraZeneca announced that it is investing $300 million in a state-of-the-art facility in Rockville, Maryland to establish life-saving cell therapy platforms for critical cancer trials and future commercial supply. To align with clinical trial timelines, the site will initially focus on pivotal clinical trial manufacturing of CAR-T cell therapies to meet current clinical supply demand. More than 150 new highly skilled jobs will be created to initially focus on manufacturing T-cell therapies to enable clinical trials to be conducted around the world. Over time, the site may expand its focus to support other therapy areas.

    Sustainability highlights

    Through the Sustainable Markets Initiative Health Systems Task Force, AstraZeneca announced an industry-first renewable power agreement in China together with four global healthcare leaders and renewable energy company Envision Energy, resulting in potential annual emissions savings of approximately 120,000 tonnes, the equivalent of taking 25,000 cars off the road. See the Sustainability section in this document for further details.

    Conference call

    A conference call and webcast for investors and analysts will begin today, 8 February 2024, at 11:45 UK time. Details can be accessed via astrazeneca.com.

    Reporting calendar

    The Company intends to publish its Q1 2024 results on 25 April 2024.

    To read AstraZeneca's Full Year and Q4 2023 Financial Results press release in full, click here.

    ______________________________

    1

    Constant exchange rates. The differences between Actual Change and CER Change are due to foreign exchange movements between periods in 2023 vs. 2022. 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.

    2

    Effective 1 January 2023, the Group has updated the presentation of Total Revenue. For further details of the presentation of Alliance Revenue and Collaboration Revenue, see the Basis of preparation and accounting policies section of the Notes to the Condensed consolidated financial statements section.

    3

    Core financial measures are adjusted to exclude certain items. The differences between Reported and Core measures are primarily due to costs relating to the acquisition of Alexion, amortisation of intangibles, impairments, legal settlements and restructuring charges. A full reconciliation between Reported EPS and Core EPS is provided in Table 13 and Table 14 in the Financial performance section of this document.

    4

    The COVID-19 medicines are Vaxzevria, Evusheld, and sipavibart (AZD3152) – the COVID-19 antibody currently in development.

    5

    The calculation of Reported and Core Product Sales Gross Margin (formerly termed as Gross Margin) excludes the impact of Alliance Revenue and Collaboration Revenue.

    6

    In Table 2, the plus and minus symbols denote the directional impact of the item being discussed, e.g. a ‘+' symbol next to an R&D expense comment indicates that the item increased the R&D expense relative to the prior year.

    7

    Income from disposals of assets and businesses, where the Group does not retain a significant ongoing economic interest, continue to be recorded in Other operating income and expense in the Company's financial statements.

    8

    Partnered with BridgeBio Pharma Inc (BridgeBio) – AstraZeneca has rights to commercialise acamoridis in Japan

     

    View source version on businesswire.com: https://www.businesswire.com/news/home/20240207868410/en/

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    2/3/26 7:01:06 AM ET
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    Biotechnology: Pharmaceutical Preparations
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    Large Ownership Changes

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    SEC Form SC 13G/A filed by AstraZeneca PLC (Amendment)

    SC 13G/A - ASTRAZENECA PLC (0000901832) (Subject)

    2/4/22 9:06:48 AM ET
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    SEC Form SC 13G/A filed

    SC 13G/A - ASTRAZENECA PLC (0000901832) (Subject)

    2/3/21 1:13:21 PM ET
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    Walmart Inc. to Join the Nasdaq-100 Index® Beginning January 20th, 2026

    NEW YORK, Jan. 09, 2026 (GLOBE NEWSWIRE) -- Nasdaq (NASDAQ:NDAQ) today announced that Walmart Inc. (NASDAQ:WMT), will become a component of the Nasdaq-100 Index® (NDX®), the Nasdaq-100 Equal Weighted™ Index (NDXE™), and the Nasdaq-100 Ex-Tech Sector™ Index (NDXX™) prior to market open on Tuesday, January 20, 2026 - the first trading day following the third Friday of the month. Walmart Inc. will replace AstraZeneca PLC (NASDAQ:AZN) in the Nasdaq-100 Index®, the Nasdaq-100 Equal Weighted Index, and the Nasdaq-100 Ex-Tech Sector Index. AstraZeneca PLC will also be removed from the Nasdaq-100 ESG™ Index (NDXESG™), Nasdaq-100 ex Top 30™​ (NDX70™), Nasdaq-100 ex Top 30​ UCITS™ (NDX70U™), Nasdaq

    1/9/26 8:00:00 PM ET
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    Vistagen Appoints Nick Tressler as Chief Financial Officer

    Vistagen (NASDAQ:VTGN), a late clinical-stage biopharmaceutical company pioneering neuroscience with nose-to-brain neurocircuitry to develop and commercialize a new class of intranasal product candidates called pherines, today announced the appointment of Nick Tressler as Chief Financial Officer (CFO), effective today, December 1, 2025. "I am excited to welcome Nick to Vistagen as our CFO. His financial and strategic acumen and extensive operational experience in the biopharmaceutical industry will be instrumental as we accelerate into our next phase," said President and Chief Executive Officer of Vistagen, Shawn Singh. "I look forward to his contributions to our leadership team and the po

    12/1/25 8:30:00 AM ET
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    Biotechnology: Pharmaceutical Preparations
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    I-Mab Appoints Phillip Dennis, MD, PhD, as Chief Medical Officer

    ROCKVILLE, Md., June 6, 2024  /PRNewswire/ -- I-Mab (NASDAQ:IMAB) (the "Company"), a U.S.-based, global biotech company, exclusively focused on the development and potential commercialization of highly differentiated immunotherapies for the treatment of cancer, today announced the appointment of Dr. Phillip Dennis as Chief Medical Officer. Dr. Dennis, who will join I-Mab effective June 17, 2024, will lead the Company's global clinical development efforts and serve as a member of I-Mab's Executive Leadership Team. "I am pleased to welcome Dr. Phillip Dennis as our Chief Medical

    6/6/24 7:00:00 AM ET
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    AstraZeneca results: FY and Q4 2025

    Strong commercial performance and excellent pipeline delivery in a continuing catalyst-rich period AstraZeneca: Revenue and EPS summary   FY 2025 % Change Q4 2025 % Change   $m Actual CER1 $m Actual CER - Product Sales 55,573 9 9 14,538 9 7 - Alliance Revenue 3,067 39 38 959 34 33 Product Revenue2 58,640 10 10 15,497 10 8 Collaboration Revenue 99 (89) (89) 6 (99) (99) Total Revenue 58,739 9 8 15,503 4

    2/10/26 7:00:00 AM ET
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    Baxdrostat New Drug Application accepted under FDA Priority Review in the US for patients with hard-to-control hypertension

    Submission based on positive BaxHTN Phase III trial results which demonstrated statistically significant and clinically meaningful reduction in systolic blood pressure in patients with resistant or uncontrolled hypertension If approved, baxdrostat could be the first aldosterone synthase inhibitor to receive regulatory authorization AstraZeneca's New Drug Application (NDA) for baxdrostat has been accepted for Priority Review by the US Food and Drug Administration (FDA) in the US for the treatment of adult patients with hard-to-control (uncontrolled or treatment resistant) hypertension as an add-on to other antihypertensive medicines when these do not provide adequate lowering of blood pres

    12/2/25 9:18:00 AM ET
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    Biotechnology: Pharmaceutical Preparations
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    Baxdrostat demonstrated a statistically significant and highly clinically meaningful placebo-adjusted reduction of 14.0 mmHg in 24-hour ambulatory systolic blood pressure in patients with resistant hypertension in the Bax24 Phase III trial

    Baxdrostat demonstrated a statistically significant placebo-adjusted reduction of 13.9 mmHg in night-time ambulatory systolic blood pressure at 12 weeks with a safety profile consistent with the BaxHTN trial Full results presented at the American Heart Association Scientific Sessions 2025 Positive full results from the Bax24 Phase III trial showed baxdrostat demonstrated a statistically significant and highly clinically meaningful reduction in ambulatory 24-hour average systolic blood pressure (SBP) compared with placebo at 12 weeks. Patients with treatment-resistant hypertension (rHTN) received baxdrostat 2mg or placebo on top of standard of care.1 Efficacy was observed throughout the

    11/9/25 4:33:00 PM ET
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    Biotechnology: Pharmaceutical Preparations
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