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AstraZeneca

AstraZeneca logo
🇬🇧United Kingdom
Ownership
Public
Employees
89.9K
Market Cap
$270.3B
Website
http://www.astrazeneca.co.uk
Introduction

AstraZeneca Plc is a holding company, which engages in the research, development, manufacture, and commercialization of prescription medicines. The company was founded on June 17, 1992 and is headquartered in Cambridge, the United Kingdom.

Clinical Trials

3.8k

Active:326
Completed:2666

Trial Phases

6 Phases

Early Phase 1:10
Phase 1:1084
Phase 2:527
+3 more phases

Drug Approvals

31

SFDA:31

Drug Approvals

FORXIGA 5 mg film-coated tablet

Approval Date
Jul 18, 2025
SFDA

TAGRISSO 40 mg Film-Coated Tablet

Approval Date
Jul 18, 2025
SFDA

INDERAL AMPULES 1MG-ML

Approval Date
Jul 18, 2025
SFDA

INDERAL TABLETS 40 MG.

Approval Date
Jul 18, 2025
Company
astrazeneca pharmaceutical ltd
SFDA

BRILINTA 90 MG FILM COATED TABLET

Approval Date
Jul 18, 2025
Company
ASTRAZENECA AB
SFDA

ATACAND 32MG TABLETS

Approval Date
Jul 18, 2025
SFDA

SEROQUEL 300MG F-C TABS

Approval Date
Jul 18, 2025
SFDA

SEROQUEL XL 50MG FILM COATED TABLET

Approval Date
Jul 18, 2025
SFDA

SYMBICORT 80 MCG/4.5 MCG TURBOHALER

Approval Date
Jul 18, 2025
SFDA

RHINOCORT AQUA 64MCG NASAL SPRAY

Approval Date
Jul 18, 2025
SFDA
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Clinical Trials

Distribution across different clinical trial phases (2772 trials with phase data)• Click on a phase to view related trials

Phase 1
1084 (39.1%)
Phase 3
893 (32.2%)
Phase 2
527 (19.0%)
Phase 4
194 (7.0%)
Not Applicable
55 (2.0%)
Early Phase 1
10 (0.4%)
phase_1_2
5 (0.2%)
phase_2_3
4 (0.1%)

An Open-label Study of AZD0120 in Adults With Multiple Sclerosis

Not Applicable
Not yet recruiting
Conditions
Multiple Sclerosis
Interventions
Biological: AZD0120 - Regimen 1
Biological: AZD0120 - Regimen 2
First Posted Date
2025-11-04
Last Posted Date
2025-11-04
Lead Sponsor
AstraZeneca
Target Recruit Count
18
Registration Number
NCT07224373
Locations
🇺🇸

Research Site, Milwaukee, Wisconsin, United States

A Phase IIb Study to Evaluate the Effect of Dapagliflozin in Combination With Baxdrostat Compared With Baxdrostat on Albuminuria in Participants With Chronic Kidney Disease and High Blood Pressure.

Not Applicable
Not yet recruiting
Conditions
Chronic Kidney Disease and Hypertension
Interventions
Drug: Baxdrostat/dapagliflozin
Drug: Baxdrostat/Placebo
First Posted Date
2025-10-30
Last Posted Date
2025-10-30
Lead Sponsor
AstraZeneca
Target Recruit Count
218
Registration Number
NCT07222917
Locations
🇬🇧

Research Site, London, United Kingdom

A Study to Assess the Safety, Tolerability, and Pharmacokinetics of a Single Ascending Dose of AZD0292 in Healthy Japanese Participants

Not Applicable
Not yet recruiting
Conditions
Healthy Participants
Interventions
Drug: Placebo
First Posted Date
2025-10-29
Last Posted Date
2025-10-29
Lead Sponsor
AstraZeneca
Target Recruit Count
18
Registration Number
NCT07222254

Study of Patient With Frequent COPD Exacerbations

Recruiting
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
First Posted Date
2025-10-29
Last Posted Date
2025-10-29
Lead Sponsor
AstraZeneca
Target Recruit Count
2000
Registration Number
NCT07221981
Locations
🇷🇺

Research site, Yekaterinburg, Russia

🇷🇺

Research site "OOO Energy of health", Saint Petersburg, Russia

Prevalence, Clinical Characteristics, Progression, and Management of Neurofibromatosis Type 1 in Egypt (NF1-Egy)

Not yet recruiting
Conditions
Neurofibromatosis Type 1
First Posted Date
2025-10-27
Last Posted Date
2025-10-27
Lead Sponsor
AstraZeneca
Target Recruit Count
200
Registration Number
NCT07221331
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News

Neok Bio Emerges with $75M to Develop Dual-Targeting ADCs for Cancer Treatment

Neok Bio launched with $75 million in Series A funding to develop bispecific antibody-drug conjugates that simultaneously target two distinct cancer proteins.

BioInvent Reports Promising Safety and Efficacy Data for Triple Combination Therapy in Relapsed/Refractory Non-Hodgkin's Lymphoma

BioInvent will present early Phase 2a data at ASH 2025 showing that the triple combination of BI-1206, rituximab, and acalabrutinib is safe and well-tolerated in relapsed/refractory NHL patients.

FDA Proposes Streamlined Biosimilar Approval Process to Reduce Drug Costs by 50%

The FDA announced new draft guidance to simplify biosimilar approval by reducing clinical testing requirements and shortening development timelines.

Alembic Pharmaceuticals Receives FDA Approval for Generic Ticagrelor 60mg Tablets for Acute Coronary Syndrome

Alembic Pharmaceuticals Limited received final FDA approval for its generic ticagrelor tablets 60mg, therapeutically equivalent to AstraZeneca's Brilinta.

AstraZeneca Establishes Sixth Global R&D Center in Beijing to Accelerate AI-Driven Drug Discovery

AstraZeneca officially opened its sixth global strategic R&D center in Beijing's BioPark, marking the company's second facility in China alongside its Shanghai center.

Trump Administration Secures Deal with EMD Serono to Cut Fertility Drug Prices by Up to 84%

President Trump announced a deal with EMD Serono to reduce fertility medication costs, with Gonal-f available at an 84% discount for IVF patients.

Cellectis Reports Promising Phase 1 Results for Lasme-cel in Relapsed/Refractory B-ALL, Advances to Pivotal Phase 2

Cellectis' allogeneic CAR-T therapy lasme-cel demonstrated a 100% overall response rate in the target Phase 2 population of heavily pretreated relapsed/refractory B-cell acute lymphoblastic leukemia patients.

Takeda Expands AI Drug Discovery Partnership with Nabla Bio in $1B+ Deal

Takeda Pharmaceutical has signed a second multi-year AI partnership with Nabla Bio, potentially worth over $1 billion including milestone payments, to accelerate early-stage drug discovery using artificial intelligence.

Activist Investor Shah Capital Calls for Novavax Sale Amid COVID Vaccine Market Share Struggles

Shah Capital, Novavax's second-largest shareholder with a 7.2% stake, has urged the company's board to pursue a sale, citing three consecutive years of poor COVID-19 vaccine performance.

Ona Therapeutics Appoints ADC Development Veteran Dr. Antoine Yver as Board Chair to Advance Breast Cancer Pipeline

Ona Therapeutics has appointed Dr. Antoine Yver, a veteran with over 35 years of oncology drug development experience, as Chair of its Board of Directors to guide the company's transition to clinical-stage operations.

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