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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:330
Completed:2652

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 (2762 trials with phase data)• Click on a phase to view related trials

Phase 1
1084 (39.2%)
Phase 3
893 (32.3%)
Phase 2
527 (19.1%)
Phase 4
194 (7.0%)
Not Applicable
45 (1.6%)
Early Phase 1
10 (0.4%)
phase_1_2
5 (0.2%)
phase_2_3
4 (0.1%)

Safety Of DAPAGLIFLOZIN (FORXIGA) in Patient With Type 2 Diabetes Mellitus (T2dm) In Vietnam From A Post-Marketing Surveillance Program

Completed
Conditions
Safety Outcomes
First Posted Date
2025-10-07
Last Posted Date
2025-10-07
Lead Sponsor
AstraZeneca
Target Recruit Count
1001
Registration Number
NCT07210307
Locations
🇻🇳

HCMC Heart Institute, Ho Chi Minh City, Vietnam

The Eplontersen Pregnancy and Lactation Outcomes Study

Not yet recruiting
Conditions
Transthyretin Amyloidosis
First Posted Date
2025-10-03
Last Posted Date
2025-10-03
Lead Sponsor
AstraZeneca
Target Recruit Count
10
Registration Number
NCT07205666

A Study of Dato-DXd in Inoperable or Metastatic Hormone Receptor-positive, HER2 IHC 0 Breast Cancer

Not Applicable
Not yet recruiting
Conditions
Breast Cancer
Interventions
First Posted Date
2025-10-03
Last Posted Date
2025-10-03
Lead Sponsor
AstraZeneca
Target Recruit Count
100
Registration Number
NCT07205822
Locations
🇪🇸

Research Site, Valencia, Spain

Study Evaluating Safety, Tolerability, PK/PD of Surovatamig in Adult RA or SLE Participants

Not Applicable
Not yet recruiting
Conditions
Rheumatoid Arthritis
Systemic Lupus Erythematosus
Interventions
Biological: Surovatamig
First Posted Date
2025-10-01
Last Posted Date
2025-10-01
Lead Sponsor
AstraZeneca
Target Recruit Count
48
Registration Number
NCT07201558

A Study to Learn How Safe AZD6621 is, How Well it Works, and How it Moves Throughout the Body Over Time, in Adult Male Participants With Metastatic Prostate Cancer

Not Applicable
Not yet recruiting
Conditions
Prostate Cancer
Interventions
Drug: AZD6621
First Posted Date
2025-09-25
Last Posted Date
2025-09-25
Lead Sponsor
AstraZeneca
Target Recruit Count
52
Registration Number
NCT07192614
Locations
🇰🇷

Research Site, Seoul, South Korea

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News

Algen Biotechnologies Partners with AstraZeneca in $555M AI-Driven Drug Discovery Deal for Immunology Targets

Algen Biotechnologies announced a multi-target partnership with AstraZeneca worth up to $555 million to accelerate discovery of novel therapeutic targets in immunology using AI-powered drug discovery.

Amgen's Repatha Demonstrates Long-Term Cardiovascular Benefits in Phase III VESALIUS-CV Trial

Amgen's Phase III VESALIUS-CV trial met both primary endpoints, demonstrating that Repatha significantly reduces major adverse cardiovascular events in high-risk patients without prior heart attack or stroke.

Thermo Fisher Scientific Partners with AstraZeneca BioVentureHub for Collaborative R&D Innovation

Thermo Fisher Scientific's PPD clinical research business has established a new R&D partnership with AstraZeneca BioVentureHub in Gothenburg, Sweden, focusing on collaborative innovation in life sciences.

Aerska Raises $21M to Develop RNA Therapies for Brain Diseases Using Novel Delivery Platform

Irish biotech startup Aerska has secured $21 million in seed funding to develop RNA interference therapies targeting degenerative neurological diseases including Alzheimer's and Parkinson's disease.

Crystalys Therapeutics Emerges with $205M Series A to Advance Gout Treatment Dotinurad

Crystalys Therapeutics launched with $205 million in Series A funding to develop dotinurad, a URAT1 blocker for gout treatment that is already approved in Japan, China, Philippines, and Thailand.

Novartis Launches Direct-to-Patient Platform for Cosentyx with 55% Discount in US

Novartis will launch a direct-to-patient platform on November 1, 2025, offering Cosentyx at a 55% discount off list price to cash-paying patients in the US.

Combination Inhaler Reduces Asthma Attacks in Children by 45% in Landmark Trial

A randomized controlled trial of 360 children aged 5-15 found that a budesonide-formoterol combination inhaler reduced asthma attacks by 45% compared to standard salbutamol treatment.

Factor Bioscience Sues AstraZeneca and Cellectis Over Gene-Editing Patent Infringement

Factor Bioscience filed a patent lawsuit against Cellectis and AstraZeneca in Delaware federal court, alleging infringement of three foundational gene-editing patents related to mRNA TALEN technology.

AstraZeneca Launches Direct-to-Consumer Platform with Up to 70% Drug Discounts Following Trump Administration Pressure

AstraZeneca announced it will offer its diabetes drug Farxiga and asthma drug Airsupra at discounts of up to 70% through a new direct-to-consumer platform launching October 1, 2025.

AIM ImmunoTech Secures Japanese Patent for Ampligen Combination Therapy in Oncology Through 2039

AIM ImmunoTech has secured a Japanese patent covering Ampligen (rintatolimod) in combination with checkpoint inhibitors for cancer treatment, valid until December 20, 2039.

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