Friday, July 10, 2026

pharma · Chronic Obstructive Pulmonary Disease (COPD) · Non-Small Cell Lung Cancer

AstraZeneca

AstraZeneca is a pharma organization headquartered in cambridge, GB. Primary therapeutic focus areas include Chronic Obstructive Pulmonary Disease (COPD), Non-Small Cell Lung Cancer, Asthma, Advanced Solid Tumors, Not ap

1 Francis Crick Avenue, Cambridge Biomedical Campus, Cambridgeshire CB2 0AA, GB HQ
79,242 Employees
EMA registrant Type
Company details
Status
Public
HQ
1 Francis Crick Avenue, Cambridge Biomedical Campus, Cambridgeshire CB2 0AA, GB
Employees
79,242
Programs
249
Drugs
238
Patents
2

Quick answer

AstraZeneca is a pharma organization headquartered in cambridge, GB. Primary therapeutic focus areas include Chronic Obstructive Pulmonary Disease (COPD), Non-Small Cell Lung Cancer, Asthma, Advanced Solid Tumors, Not applicable, healthy volunteers. NovaPharmaNews links 249 clinical program(s), 0 drug profile(s), and 0 patent record(s) to this entity from public FDA, EMA, ClinicalTrials.gov, and USPTO sources. Pipeline phase mix: phase 3 (120), phase 2 (79), phase 1 (46).

Company snapshot

AstraZeneca maintains 249 tracked programs across Chronic Obstructive Pulmonary Disease (COPD), Non-Small Cell Lung Cancer, Asthma, Advanced Solid Tumors, Not applicable, healthy volunteers, Chronic kidney disease (CKD) and hypertension., Metastatic Prostate Cancer, Locoregional Hepatocellular Carcinoma (HCC), Neurofibromatosis Type 1 (NF1) Related Plexiform Neurofibromas (PN), Breast Cancer, Chro

  • 249 active pipeline program(s) linked via ClinicalTrials.gov.
  • 2 US patent(s) indexed to this assignee profile.
  • 249 trial update(s) in the last 12 months.

Public regulatory, clinical, patent, and corporate records for AstraZeneca. Not investment advice.

Catalysts

Upcoming readouts, regulatory dates, and congress activity.

  • approval

    Daiichi and AstraZeneca's Enhertu: Early Breast Cancer Breakthrough

  • approval

    FDA Approval for Datroway: Implications for Breast Cancer Treatment

  • deal

    AstraZeneca's Breast Cancer Pill and ADAP Deal Insights

  • approval

    Imfinzi Receives FDA Approval for Bladder Cancer Treatment

  • approval

    IMFINZI® Approved for High-Risk Bladder Cancer: A Game Changer

  • approval

    FDA Delays AstraZeneca's Breast Cancer Drug Review: Key Insights

  • approval

    ASCO26: AstraZeneca's Camizestrant Data Aims to Sway FDA Approval

  • approval

    ASCO 2026: European Pharma's Quiet Showing and What AstraZeneca & Roche Must Address

  • approval

    Datroway Priority Review Fuels Hope for Metastatic Triple-Negative Breast Cancer Patients

  • approval

    AbbVie's Decnupaz Secures FDA Approval for Rare Blood Cancer

  • approval

    FDA Approves AstraZeneca's Imfinzi-BCG Combination for High-Risk NMIBC

  • approval

    FDA Approves Baxdrostat (Baxfendy) as First Aldosterone Synthase Inhibitor for Uncontrolled Hypertension

Recent coverage

Truqap gains US approval in PTEN-deficient metastatic prostate cancer
High impact Newsprostate cancerJun 13, 2026

Truqap gains US approval in PTEN-deficient metastatic prostate cancer

FDA · prostate cancer · 6 min

AstraZeneca’s Truqap (capivasertib) has been approved in the US with abiraterone and prednisone for PTEN-deficient metastatic prostate cancer. The move creates a first-in-class targeted option and a new catalyst to watch for BD teams, investors, and analysts.

Dr. Elena Rossi
AstraZeneca expands obesity push as it invests $125M in ultrasound medicine
High impact NewsobesityJun 11, 2026

AstraZeneca expands obesity push as it invests $125M in ultrasound medicine

FDA · obesity · 5 min

AstraZeneca’s obesity strategy widened after newly published data supported a sprawling late-stage program for its GLP-1 pill. The company also committed $125 million to ultrasound-aided genetic medicine, signaling continued platform investing.

Dr. Sarah Mitchell
PMDA approves ENHERTU for HER2-low breast cancer in Japan
High impact NewsJun 10, 2026

PMDA approves ENHERTU for HER2-low breast cancer in Japan

5 min

PMDA approved ENHERTU for unresectable or metastatic HER2-low breast cancer in Japan, marking a new regulatory catalyst for Daiichi Sankyo and AstraZeneca. The decision expands the drug’s labeled use in a major market and adds another milestone for investors tracking ENHERTU.

Dr. Yuki Tanaka
EMA backs datopotamab deruxtecan, but lung cancer access remains unclear
Critical impact Analysislung cancerJun 7, 2026

EMA backs datopotamab deruxtecan, but lung cancer access remains unclear

EMA · lung cancer · 9 min

EMA recommended datopotamab deruxtecan in Europe, but the supported EU approval in the evidence base is for HR-positive, HER2-negative breast cancer rather than lung cancer. In the U.S., DATROWAY has accelerated approval for EGFR-mutated NSCLC, making this a key catalyst-tracking update for BD teams and investors.

Dr. Sarah Mitchell

Lead pipeline drugs

Active clinical programs

  • ADAURA - D5164C00001 Stage IB-IIIA non-small cell lung carcinoma, with a centrally confirmed, common sensitising EGFR mutations (Ex19del and L858R either alone or in combination with other EGFR mutations), following complete tumour resection with or without adjuvant chemotherapy
    Phase 3
  • AZD0780 Placebo, AZD0780 Heterozygous familial hypercholesterolaemia
    Phase 3
  • AZD0780, AZD0780 Placebo Hyperlipidemia, Atherosclerotic cardiovascular disease
    Phase 3
  • AZD0780, AZD0780 placebo Atherosclerotic Cardiovascular Disease
    Phase 3

Momentum

Proprietary activity score for AstraZeneca.

2 active signals

25 /100 +0 vs 30 days ago

Signal breakdown

  • Clinical trials 0 30d
  • Nova articles 31 30d
  • Patents filed 0 30d
  • FDA actions 0 30d
  • SEC filings 0 30d
  • Conference presentations 14 90d
  • Pipeline advances 0 30d

Competitor landscape

Therapeutic-area overlap peers from registry and pipeline signals.

Recent activity

Latest pipeline, patent, and corporate events for AstraZeneca.

  1. Clinical update

    IRIS, D3466C00001 — Phase 3

  2. Clinical update

    D8530C00001 — Phase 1

  3. Clinical update

    D5180C00016 — Phase 3

  4. Clinical update

    D5162C00048 — Phase 2

  5. Clinical update

    D5084C00016 — Phase 1

View all clinical trial activity →

Quick answers

Common questions about this sponsor — for analysts and search.

  • What is AstraZeneca?

    AstraZeneca is a pharma organization headquartered in cambridge, GB. Primary therapeutic focus areas include Chronic Obstructive Pulmonary Disease (COPD), Non-Small Cell Lung Cancer, Asthma, Advanced Solid Tumors, Not applicable, healthy volunteers. NovaPharmaNews links 249 clini

  • Is AstraZeneca publicly traded?

    AstraZeneca appears in our database through regulatory marketing authorisation or clinical trial sponsor records; a US listed ticker is not shown for this entity.

  • What drugs does AstraZeneca develop or market?

    We link 238 drug profile(s) where AstraZeneca is an originator or marketer in FDA or regional approval metadata. See the drug portfolio table on https://novapharmanews.com/companies/astrazeneca-ab#company-drugs.

  • What are the latest developments for AstraZeneca?

    In the last 12 months our linked public records show 249 trial program update(s) and 0 US patent grant(s) tied to this profile.

  • What therapeutic areas does AstraZeneca focus on?

    AstraZeneca focuses on Chronic Obstructive Pulmonary Disease (COPD), Non-Small Cell Lung Cancer, Asthma based on our analysis of their pipeline programs and drug development activities.

Full intelligence profile

Registry synthesis

Grounded overview from trials, patents, coverage, and catalysts.

AstraZeneca maintains 249 tracked programs across Chronic Obstructive Pulmonary Disease (COPD), Non-Small Cell Lung Cancer, Asthma, Advanced Solid Tumors, Not applicable, healthy volunteers, Chronic kidney disease (CKD) and hypertension., Metastatic Prostate Cancer, Locoregional Hepatocellular Carcinoma (HCC), Neurofibromatosis Type 1 (NF1) Related Plexiform Neurofibromas (PN), Breast Cancer, Chronic Heart Failure, Triple-negative Breast Cancer. Momentum score: 25/100 (30-day delta: n/a).

Public registry data covers pipeline phase, clinical trials, patents, SEC filings, and Nova editorial coverage. HQ: cambridge GB. Ticker: EBA8A89.

Pipeline programs

D7632C00001 — phase phase_3, status active. Indication: Locally-advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) with high PD-L1 expression (TC ≥ 50%) and without actionable genomic alterations.. Next milestone: not disclosed (TBD).

D8991C00001 — phase phase_3, status active. Indication: Advanced Platinum-resistant Epithelial Ovarian Cancer. Next milestone: not disclosed (TBD).

D516FC00001(ADAURA2) — phase phase_3, status active. Indication: Stage IA2-IA3 non-small cell lung carcinoma, with EGFR mutation type (Ex19del, L858R), following complete tumour resection.. Next milestone: not disclosed (TBD).

D7402C00001 — phase phase_3, status active. Indication: Large B-cell Lymphoma. Next milestone: not disclosed (TBD).

D8534C00001 — phase phase_3, status active. Indication: Estrogen Receptor-Positive, HER-2 negative Advanced Breast Cancer. Next milestone: not disclosed (TBD).

D8610C00001 — phase phase_3, status active. Indication: Respiratory Syncytial Virus and Human Metapneumovirus. Next milestone: not disclosed (TBD).

D6185C00001 — phase phase_3, status active. Indication: Patients with non-small cell lung cancer (NSCLC).. Next milestone: not disclosed (TBD).

D5241C00006 — phase phase_3, status active. Indication: Chronic obstructive pulmonary disease (COPD). Next milestone: not disclosed (TBD).

D6402C00012 — phase phase_3, status active. Indication: Chronic HF and comorbid impairment of kidney function who had a recent HF event to evaluate the effect of balcinrenone/dapagliflozin versus dapagliflozin alone on HF events and cardiovascular (CV) death. Next milestone: not disclosed (TBD).

D7310C00001 — phase phase_3, status active. Indication: Patients With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck Previously Treated With an Immune Checkpoint Inhibitor. Next milestone: not disclosed (TBD).

D8311C00001 — phase phase_3, status active. Indication: Relapsed or Refractory Multiple Myeloma. Next milestone: not disclosed (TBD).

D6900C00003 — phase phase_3, status active. Indication: B7-H4-Selected Advanced/Metastatic Endometrial Cancer.. Next milestone: not disclosed (TBD).

Recent Nova coverage

Nova coverage: Truqap gains US approval in PTEN-deficient metastatic prostate cancer (2026-06-13).

Nova coverage: AstraZeneca expands obesity push as it invests $125M in ultrasound medicine (2026-06-11).

Nova coverage: PMDA approves ENHERTU for HER2-low breast cancer in Japan (2026-06-10).

Nova coverage: EMA backs datopotamab deruxtecan, but lung cancer access remains unclear (2026-06-07).

Nova coverage: EMA backs datopotamab deruxtecan for advanced lung cancer (2026-06-07).

Nova coverage: AstraZeneca and Daiichi Sankyo datopotamab deruxtecan hits lung cancer endpoint (2026-06-07).

Nova coverage: 5 Notable Oncology FDA Approvals Granted in May: A B2B Analysis (2026-06-06).

Nova coverage: Pharma bets on PD-1/VEGF bispecifics: Is lung cancer the wrong target? (2026-06-06).

Registry facts

Registry profile: founded unknown; employees 79242; market cap n/a; revenue n/a; LEI 636700ITSLXVAJVLAY33; CIK n/a.

Company type: pharma; public/private: public. Data quality score: 0.833.

Catalyst calendar

Catalyst: Daiichi and AstraZeneca's Enhertu: Early Breast Cancer Breakthrough — type approval, date 2026-05-19.

Catalyst: FDA Approval for Datroway: Implications for Breast Cancer Treatment — type approval, date 2026-05-23.

Catalyst: AstraZeneca's Breast Cancer Pill and ADAP Deal Insights — type deal, date 2026-05-27.

Catalyst: Imfinzi Receives FDA Approval for Bladder Cancer Treatment — type approval, date 2026-05-30.

Catalyst: IMFINZI® Approved for High-Risk Bladder Cancer: A Game Changer — type approval, date 2026-05-30.

Catalyst: FDA Delays AstraZeneca's Breast Cancer Drug Review: Key Insights — type approval, date 2026-06-01.

Catalyst: ASCO26: AstraZeneca's Camizestrant Data Aims to Sway FDA Approval — type approval, date 2026-06-02.

Catalyst: ASCO 2026: European Pharma's Quiet Showing and What AstraZeneca & Roche Must Address — type approval, date 2026-06-02.

Catalyst: Datroway Priority Review Fuels Hope for Metastatic Triple-Negative Breast Cancer Patients — type approval, date 2026-06-02.

Catalyst: AbbVie's Decnupaz Secures FDA Approval for Rare Blood Cancer — type approval, date 2026-06-02.

Competitive peers

Peer: AstraZeneca (overlap score 50.0).

Peer: BEONE MEDICINES AUS (overlap score 50.0).

Peer: Novartis India (overlap score 40.0).

Peer: Sunshine Guojian Pharmaceutical (overlap score 40.0).

Peer: HOFFMANN-LA ROCHE (overlap score 40.0).

Peer: Amgen (overlap score 39.2).

Peer: Eli Lilly and (overlap score 32.4).

Peer: ADC Therapeutics (overlap score 26.0).

Competitive positioning reflects therapeutic-area overlap with peer sponsors and recent catalyst activity from trials, regulatory actions, and congress presentations. Data is assembled from ClinicalTrials.gov, SEC EDGAR, openFDA, and NovaPharmaNews articles — not third-party wire republication.

Therapeutic focus

Therapeutic area distribution

Pipeline concentration by therapeutic area from linked clinical programs.

Programs by therapeutic area

Others
166
Oncology
114
Cardiology
23
Infectious Disease
13
Neurology
6
Immunology
5
Rare Disease
1
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