TOP-LINE RESULTS FROM LYNPARZA GOLD TRIAL


ASTRAZENECA PROVIDES TOP-LINE RESULTS FROM LYNPARZA GOLD TRIAL IN ADVANCED
GASTRIC CANCER

18 May 2016

AstraZeneca today announced that Lynparza (olaparib) in combination with
paclitaxel chemotherapy, compared with paclitaxel chemotherapy alone, did not
meet the primary endpoint of overall survival (OS) in the Phase III GOLD trial
in advanced gastric cancer patients, in either the overall population or
patients whose tumour tested negative for Ataxia-Telangectasia Mutated (ATM)
protein. Whilst there was a numerical survival trend in the Lynparza plus
paclitaxel arm, it did not meet statistical significance.

Sean Bohen, Executive Vice President, Global Medicines Development and Chief
Medical Officer at AstraZeneca, said: "While there was a numerical trend for
survival benefit with Lynparza plus paclitaxel in the GOLD trial, we are
disappointed that this did not reach statistical significance. The particular
regimen in the GOLD study, at a low dose and in combination with chemotherapy,
differs from other Phase III trials in the Lynparza programme. We look forward
to presenting the GOLD data and remain confident in Lynparza's clinical activity
in a range of tumour types, including its approved use in BRCA-mutated ovarian
cancer."

GOLD was a randomised, double-blinded, placebo-controlled, multicentre Phase III
trial to assess the efficacy and safety of Lynparza in combination with
paclitaxel, compared with paclitaxel alone. The trial enrolled Asian patients
with advanced HER2-negative gastric cancer (including the gastro-oesophageal
junction) who had progressed following 1st-line therapy. The trial, conducted in
China, Japan, South Korea and Taiwan where gastric cancer is particularly
prevalent, enrolled a total of 525 patients - 18% of whom had tumours that
tested ATM negative by immunohistochemistry (IHC). Lynparza was given orally at
a dose of 100mg twice daily in combination with paclitaxel IV infusion over 1
hour at 80mg/m2 weekly on days 1, 8 and 15 of a 28 day schedule.

The reported incidence of adverse events for Lynparza in combination with
paclitaxel compared with paclitaxel alone was similar.

A full evaluation of the data is ongoing and the results will be submitted for
presentation at an upcoming medical meeting.

Lynparza is approved in over 40 countries for use as monotherapy for the
maintenance treatment of adult patients with platinum-sensitive relapsed BRCA
-mutated (germline and/or somatic) high grade serous epithelial ovarian,
fallopian tube or primary peritoneal cancer who are in response (complete or
partial) to platinum-based chemotherapy. It is approved in the US as monotherapy
in patients with deleterious or suspected deleterious germline BRCA-mutated
advanced ovarian cancer who have been treated with three or more prior lines of
chemotherapy.

About Gastric Cancer
Gastric and Gastroesophageal Junction (GEJ) adenocarcinomas account for around
84% of all cancers of the stomach. The incidence of gastric cancer (GC) is
disproportionally high in East Asia, where annual incidence is around 9 times
higher than those in the G6 countries combined.¹

About Lynparza
Lynparza (olaparib) is an innovative, first-in-class oral poly ADP-ribose
polymerase (PARP) inhibitor that exploits tumour DNA damage response (DDR)
pathway deficiencies to preferentially kill cancer cells. Lynparza is the
foundation of AstraZeneca's industry-leading portfolio of compounds targeting
DNA damage response (DDR) mechanisms in cancer cells. Lynparza is the first PARP
inhibitor to be approved by regulatory authorities in the EU and US for the
treatment of women with BRCA-mutated (BRCAm) ovarian cancer.

About AstraZeneca in Oncology
AstraZeneca has a deep-rooted heritage in Oncology and offers a quickly growing
portfolio of new medicines that has the potential to transform patients' lives
and the Company's future. With at least 6 new medicines to be launched between
2014 and 2020 and a broad pipeline of small molecules and biologics in
development, we are committed to advance New Oncology as one of AstraZeneca's
six Growth Platforms focused on lung, ovarian, breast and blood cancers. In
addition to our core capabilities, we actively pursue innovative partnerships
and investments that accelerate the delivery of our strategy, as illustrated by
our investment in Acerta Pharma in haematology.

By harnessing the power of four scientific platforms -- immuno-oncology, the
genetic drivers of cancer and resistance, DNA damage response and antibody drug
conjugates -- and by championing the development of personalised combinations,
AstraZeneca has the vision to redefine cancer treatment and one day eliminate
cancer as a cause of death.

About AstraZeneca
AstraZeneca is a global, innovation-driven biopharmaceutical business that
focuses on the discovery, development and commercialisation of prescription
medicines, primarily for the treatment of diseases in three main therapy areas -
respiratory, inflammation, autoimmune disease (RIA), cardiovascular and
metabolic disease (CVMD) and oncology - as well as in infection and
neuroscience. AstraZeneca operates in over 100 countries and its innovative
medicines are used by millions of patients worldwide. For more information
please visit: www.astrazeneca.com

CONTACTS

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|Eugenia Litz            |RIA                     |+44 7884 735627
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|Nick Stone              |CVMD, RIA               |+44 7717 618834
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|Lindsey Trickett        |Oncology, ING           |+1 240 543 7970
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Key: RIA - Respiratory, Inflammation and Autoimmunity, CVMD - Cardiovascular and
Metabolic Disease, ING - Infection, Neuroscience and Gastrointestinal

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18 May 2016

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