| 2020-03-03 |
6-K |
ANNUAL FINANCIAL REPORT |
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| 2020-03-02 |
6-K |
TOTAL VOTING RIGHTS |
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| 2020-03-02 |
6-K |
ASTRAZENECA COMPLETES DIVESTMENT AGREEMENT WITH ATNAHS PHARMA FOR ESTABLISHED HY |
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| 2020-02-27 |
6-K |
DIRECTOR/PDMR SHAREHOLDING |
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| 2020-02-25 |
6-K |
ASTRAZENECA DIVESTS GLOBAL RIGHTS TO MOVANTIK |
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| 2020-02-19 |
6-K |
DIRECTOR/PDMR SHAREHOLDING |
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| 2020-02-14 |
6-K |
AZN: FULL-YEAR AND Q4 2019 RESULTS |
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| 2020-02-07 |
4 |
4 |
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| 2020-02-07 |
3 |
3 |
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| 2020-02-07 |
SC 13D |
SC 13D |
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| 2020-02-06 |
EFFECT |
|
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| 2020-02-05 |
SC 13G/A |
|
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| 2020-02-03 |
6-K |
TOTAL VOTING RIGHTS |
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| 2020-01-30 |
SC 13G |
SC 13G |
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| 2020-01-27 |
SC 13G/A |
SEC SCHEDULE 13G |
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| 2020-01-27 |
6-K |
PHASE II DESTINY-GASTRIC01 TRIAL OF ENHERTU VERSUS CHEMOTHERAPY MET PRIMARY ENDP |
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| 2020-01-27 |
6-K |
ASTRAZENECA TO RECOVER THE GLOBAL RIGHTS TO BRAZIKUMAB (MEDI2070) FROM ALLERGAN |
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| 2020-01-27 |
6-K |
BRILINTA MET PRIMARY ENDPOINT IN PHASE III THALES TRIAL IN STROKE |
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| 2020-01-27 |
6-K |
ASTRAZENECA DIVESTS RIGHTS TO ESTABLISHED HYPERTENSION MEDICINES |
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| 2020-01-22 |
F-6 |
FORM F-6 |
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| 2020-01-21 |
6-K |
LYNPARZA REGULATORY SUBMISSION GRANTED PRIORITY REVIEW IN THE US FOR HRR-MUTATED |
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| 2020-01-21 |
6-K |
IMFINZI AND TREMELIMUMAB GRANTED ORPHAN DRUG DESIGNATION IN THE US FOR LIVER CAN |
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| 2020-01-13 |
6-K |
LYNPARZA REGULATORY SUBMISSION GRANTED PRIORITY REVIEW IN THE US FOR 1ST-LINE MA |
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| 2020-01-13 |
6-K |
UPDATE ON PHASE III STRENGTH TRIAL FOR EPANOVA IN MIXED DYSLIPIDAEMIA |
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| 2020-01-06 |
6-K |
LOKELMA APPROVED IN CHINA FOR THE TREATMENT OF ADULT PATIENTS WITH HYPERKALAEMIA |
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| 2020-01-06 |
6-K |
FARXIGA GRANTED FDA PRIORITY REVIEW FOR PATIENTS WITH HEART FAILURE WITH REDUCED |
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| 2020-01-02 |
6-K |
TOTAL VOTING RIGHTS |
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| 2019-12-30 |
6-K |
LYNPARZAAPPROVED IN THE US AS A 1ST-LINE MAINTENANCE TREATMENT OF GERMLINE BRCA- |
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| 2019-12-23 |
6-K |
ASTRAZENECA'S TRIPLE-COMBINATION THERAPY APPROVED IN CHINA FOR PATIENTS WITH COP |
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| 2019-12-23 |
6-K |
ENHERTU (TRASTUZUMAB DERUXTECAN) APPROVED IN THE US FOR HER2-POSITIVE UNRESECTAB |
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| 2019-12-20 |
6-K |
ASTRAZENECA DIVESTS RIGHTS TO ARIMIDEX AND CASODEX IN EUROPE AND CERTAIN ADDITIO |
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| 2019-12-17 |
6-K |
FDA PANEL BACKS LYNPARZA USE FOR PANCREATIC CANCER |
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| 2019-12-16 |
6-K |
SEROQUEL RIGHTS AGREEMENT COMPLETE: EUROPE, RUSSIA |
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| 2019-12-12 |
6-K |
IMFINZI APPROVED IN CHINA FOR THE TREATMENT OF UNRESECTABLE, STAGE III NON-SMALL |
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| 2019-12-11 |
6-K |
TRASTUZUMAB DERUXTECAN ACHIEVED A TUMOUR RESPONSE RATE OF 60.9% IN PIVOTAL PHASE |
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| 2019-12-05 |
6-K |
LYNPARZA APPROVED IN CHINA AS A 1ST-LINE MAINTENANCE THERAPY IN BRCA-MUTATED ADV |
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| 2019-12-03 |
6-K |
ASTRAZENECA DIVESTS RIGHTS TO SEROQUEL AND SEROQUEL XR IN THE US AND CANADA |
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| 2019-12-02 |
6-K |
BLOCK LISTING INTERIM REVIEW |
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| 2019-12-02 |
6-K |
TOTAL VOTING RIGHTS |
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| 2019-11-29 |
6-K |
IMFINZI GRANTED FDA PRIORITY REVIEW FOR THE TREATMENT OF PATIENTS WITH EXTENSIVE |
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| 2019-11-21 |
6-K |
CALQUENCE APPROVED IN THE US FOR ADULT PATIENTS WITH CHRONIC LYMPHOCYTIC LEUKAEM |
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| 2019-11-15 |
6-K |
QTRILMET APPROVED IN THE EU FOR TREATMENT OF T2D |
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| 2019-11-14 |
6-K |
FDA ACCEPTS REGULATORY SUBMISSION FOR SELUMETINIB |
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| 2019-11-12 |
6-K |
ANIFROLUMAB DEMONSTRATED SUPERIORITY ACROSS MULTIPLE EFFICACY ENDPOINTS IN PATIE |
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| 2019-11-12 |
6-K |
ROXADUSTAT PHASE III PROGRAMME POOLED ANALYSES SHOWED POSITIVE EFFICACY AND NO I |
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| 2019-11-08 |
6-K |
ROXADUSTAT SIGNIFICANTLY INCREASED HAEMOGLOBIN LEVELS FOR CHRONIC KIDNEY DISEASE |
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| 2019-11-08 |
F-3ASR |
FORM F-3ASR |
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| 2019-11-06 |
6-K |
CALQUENCE DATA TO SHOW IMPROVED PROGRESSION-FREE SURVIVAL IN PHASE III FRONT-LIN |
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| 2019-11-01 |
6-K |
TOTAL VOTING RIGHTS |
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| 2019-10-30 |
6-K |
ASTRAZENECA DIVESTS RIGHTS TO SEROQUEL AND SEROQUEL XR IN EUROPE AND RUSSIA |
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| 2019-10-28 |
6-K |
IMFINZI AND IMFINZI PLUS TREMELIMUMAB DELAYED |
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| 2019-10-25 |
SC 13D |
SC 13D |
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| 2019-10-24 |
6-K |
ASTRAZENECA YEAR-TO-DATE AND Q3 2019 RESULTS |
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| 2019-10-21 |
6-K |
FARXIGA APPROVED IN THE US TO REDUCE THE RISK OF HOSPITALISATION FOR HEART FAILU |
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| 2019-10-17 |
6-K |
TRASTUZUMAB DERUXTECAN GRANTED FDA PRIORITY REVIEW FOR TREATMENT OF PATIENTS WIT |
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| 2019-10-09 |
4 |
FORM 4 SUBMISSION |
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| 2019-10-09 |
3/A |
FORM 3/A SUBMISSION |
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| 2019-10-04 |
6-K |
HOLDING(S) IN COMPANY |
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| 2019-10-04 |
6-K |
HOLDING(S) IN COMPANY |
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| 2019-10-04 |
6-K |
FASENRA APPROVED IN THE US FOR SELF-ADMINISTRATION |
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| 2019-10-03 |
6-K |
DIRECTOR DECLARATION |
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| 2019-10-02 |
3 |
FORM 3 SUBMISSION |
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| 2019-10-01 |
6-K |
TOTAL VOTING RIGHTS |
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| 2019-10-01 |
6-K |
ASTRAZENECA DIVESTS RIGHTS FOR LOSEC TO CHEPLAPHAR |
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| 2019-10-01 |
6-K |
UPDATE ON US REGULATORY REVIEW OF PT010 IN COPD |
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| 2019-09-30 |
6-K |
LYNPARZA MORE THAN DOUBLED THE TIME WITHOUT RADIOGRAPHIC DISEASE PROGRESSION IN |
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| 2019-09-30 |
6-K |
LYNPARZA IMPROVED THE TIME WOMEN LIVED WITHOUT DISEASE PROGRESSION TO 22 MONTHS |
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| 2019-09-30 |
6-K |
TAGRISSO IS THE ONLY 1ST-LINE TREATMENT FOR EGFR-MUTATED NON-SMALL CELL LUNG CAN |
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| 2019-09-23 |
6-K |
QTRILMET RECOMMENDED FOR APPROVAL IN EU BY CHMP |
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| 2019-09-18 |
25-NSE |
|
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| 2019-09-18 |
6-K |
ASTRAZENECA AMENDS COLLABORATION WITH IRONWOOD FOR LINZESS IN CHINA |
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| 2019-09-09 |
6-K |
IMFINZI IS FIRST IMMUNOTHERAPY TO SHOW BOTH SIGNIFICANT SURVIVAL BENEFIT AND IMP |
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| 2019-09-04 |
6-K |
TAGRISSO APPROVED IN CHINA AS A 1ST-LINE TREATMENT FOR EGFR-MUTATED NON-SMALL CE |
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| 2019-09-03 |
6-K |
TOTAL VOTING RIGHTS |
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| 2019-09-03 |
6-K |
DETAILED RESULTS FROM PHASE III DAPA-HF TRIAL SHOWED FARXIGA SIGNIFICANTLY REDUC |
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| 2019-09-03 |
6-K |
BRILINTA REDUCED THE RISK OF CARDIOVASCULAR EVENTS IN PATIENTS WITH CORONARY ART |
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| 2019-08-29 |
6-K |
ANIFROLUMAB PHASE III TRIAL MEETS PRIMARY ENDPOINT IN SYSTEMIC LUPUS ERYTHEMATOS |
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| 2019-08-28 |
6-K |
BREZTRI AEROSPHERE PHASE III ETHOS TRIAL MET ITS PRIMARY ENDPOINT IN CHRONIC OBS |
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| 2019-08-28 |
6-K |
FASENRA GRANTED US ORPHAN DRUG DESIGNATION FOR EOSINOPHILIC OESOPHAGITIS |
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| 2019-08-22 |
6-K |
ROXADUSTAT APPROVED IN CHINA FOR THE TREATMENT OF ANAEMIA IN NON-DIALYSIS-DEPEND |
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| 2019-08-22 |
6-K |
ASTRAZENECA AGREES TO BUY US FDA PRIORITY REVIEW |
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| 2019-08-21 |
6-K |
UPDATE ON THE PHASE III NEPTUNE TRIAL |
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| 2019-08-20 |
6-K |
FARXIGA MET PRIMARY ENDPOINT IN LANDMARK PHASE III |
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| 2019-08-19 |
6-K |
DIRECTORATE CHANGE |
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| 2019-08-14 |
6-K |
CALQUENCE GRANTED US BREAKTHROUGH THERAPY DESIGNATION |
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| 2019-08-14 |
6-K |
LYNPARZA PHASE III PAOLA-1 TRIAL MET PRIMARY ENDPOINT |
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| 2019-08-09 |
6-K |
TAGRISSO SIGNIFICANTLY IMPROVES OVERALL SURVIVAL |
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| 2019-08-07 |
6-K |
LYNPARZA PHASE III PROFOUND TRIAL IN HRR* |
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| 2019-08-05 |
6-K |
FORXIGA LABEL UPDATED IN THE EU IN TYPE-2 DIABETES |
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| 2019-08-01 |
6-K |
TOTAL VOTING RIGHTS |
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| 2019-07-25 |
6-K |
6-K |
View Document |
| 2019-07-15 |
6-K |
UPDATE ON US REGULATORY DECISION FOR FARXIGA |
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| 2019-07-12 |
6-K |
IMFINZI GRANTED US ORPHAN DRUG DESIGNATION FOR SMALL CELL LUNG CANCER |
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| 2019-07-01 |
6-K |
FASENRA RECEIVES POSITIVE EU CHMP OPINION FOR SELF |
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| 2019-07-01 |
6-K |
TOTAL VOTING RIGHTS |
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| 2019-07-01 |
6-K |
FORXIGA RECEIVES POSITIVE EU CHMP OPINION FOR |
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| 2019-06-27 |
11-K |
|
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| 2019-06-27 |
6-K |
IMFINZI IMPROVES OVERALL SURVIVAL AT INTERIM |
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| 2019-06-19 |
6-K |
BREZTRI AEROSPHERE (PT010) APPROVED IN JAPAN FOR PATIENTS WITH CHRONIC OBSTRUCTI |
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| 2019-06-19 |
6-K |
LYNPARZA APPROVED IN JAPAN FOR 1ST-LINE MAINTENANCE THERAPY IN BRCA-MUTATED ADVA |
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