Skip to main content

Directors' Report:
Our performance

Pipeline

Compound Mechanism Areas under investigation Phase Estimated filing date
NCEs I II III Europe US
PN400 naproxen + esomeprazole signs and symptoms of OA, RA, and AS selected selected selected 1H 2009 1H 2009
AZD3480 neuronal nicotinic receptor agonist cognitive disorders in schizophrenia selected selected 2011 2011
AZD3480 neuronal nicotinic receptor agonist Alzheimer’s disease selected selected 2011 2011
AZD6765 NMDA receptor antagonist depression selected selected
AZD2327 enkephalinergic receptor modulator anxiety and depression selected
AZD5904 inhibitor of myeloperoxidase (MPO) multiple sclerosis selected
AZD3241 inhibitor of myeloperoxidase (MPO) Parkinson’s disease selected
AZD0328 selective neuronal nicotinic receptor agonist Alzheimer’s disease selected
AZD1940 CB receptor agonist nociceptive and neuropathic pain selected
AZD2624 NK receptor antagonist schizophrenia selected
AZD1386 vanilloid receptor antagonist chronic nociceptive pain selected
AZD2066 metabotropic glutamate receptors chronic nociceptive pain selected
AZD7325 GABA receptor subtype partial agonist anxiety selected
AZD6280 GABA receptor subtype partial agonist anxiety selected
TC-5619 (Targacept) neuronal nicotinic receptor agonist cognitive disorders in schizophrenia selected
 
Line extensions
Seroquel XR D2/5HT2 antagonist schizophrenia selected selected selected Approved Launched
Seroquel D2/5HT2 antagonist bipolar maintenance selected selected selected 2Q 2008 Filed
Seroquel D2/5HT2 antagonist bipolar depression selected selected selected 1Q 2008 Launched
Seroquel XR D2/5HT2 antagonist generalised anxiety disorder selected selected selected 4Q 2008 2Q 2008
Seroquel XR D2/5HT2 antagonist major depressive disorder selected selected selected 3Q 2008 1Q 2008
Seroquel XR D2/5HT2 antagonist bipolar mania selected selected selected 1Q 2008 Filed
Seroquel XR D2/5HT2 antagonist bipolar depression selected selected selected 1Q 2008 Filed

For discontinued projects see the Development Pipeline section.

Our product pipeline and life cycle management work is focused on the important areas of pain control, psychiatry, analgesia, neurology and anaesthesia. In 2007, we have significantly strengthened the early development pipeline by progressing 10 additional compounds into clinical testing. Although it was decided in 2006 not to start new discovery work in Parkinson’s disease (PD), multiple sclerosis (MS) and neuroprotection in stroke, current projects in development for PD and MS continue as planned.

Pain control

PN400 is a fixed-dose combination tablet of naproxen and esomeprazole which uses proprietary technology licensed from POZEN Inc. through a partnership established in August 2006. It is being developed for the relief of signs and symptoms of osteoarthritis, rheumatoid arthritis and ankylosing spondylitis in patients at risk for developing non-steroidal anti-inflammatory drug (NSAID)-associated gastric ulcers. At least 50% of the 60 million osteoarthritis patients in the US and the five largest European countries are at risk of developing NSAID-associated ulcers.

A phase III trial programme, which was initiated in the third quarter of 2007, is evaluating the incidence of gastric ulcers in at-risk patients with chronic pain taking PN400 versus the ulcer incidence in those taking naproxen alone. A regulatory submission for PN400 in the US is currently planned for the first half of 2009.

Psychiatry

We progressed four compounds, AZD6765, AZD2624, AZD6280 and AZD7325, into clinical development for the treatment of anxiety, schizophrenia and/or depression. We also entered into a collaboration with the University of Texas Southwestern Medical Center at Dallas, US to accelerate scientific discovery and therapeutic advancement for depression.

Analgesia

We have progressed three compounds, AZD2066, AZD1940 and AZD1386 into phase I clinical development for the treatment of nociceptive (caused by tissue damage) and/or neuropathic (caused by nerve damage) pain.

In October 2007, by mutual agreement with NPS Pharmaceuticals, Inc. we decided to end our collaborative efforts to discover and develop drugs targeting metabotropic glutamate receptors (mGluRs). As part of this agreement, we have acquired certain know-how, intellectual property and technology rights from NPS Pharmaceuticals for our exclusive use.

We have established a partnership with the University of Texas M. D. Anderson Cancer Center to develop platforms and clinical targets for new drugs in chronic pain.

Neurology

We continue to expand our research capabilities in positron emission tomography (PET) through our collaboration with the Karolinska Institute in Sweden, providing early signalling of potential efficacy for our Alzheimer’s compounds. In addition, we have established two Alzheimer’s alliances with key US centres, the Banner Alzheimer’s Institute in Phoenix, Arizona and Washington University in St. Louis. Both approaches are focused on the identification and progression of Alzheimer’s disease. We currently have eight development programmes, of which six are in clinical evaluation, in Alzheimer’s disease, cognitive disorders in schizophrenia (CDS) and specific segments of other neuro-degenerative diseases, multiple sclerosis and Parkinson’s disease.

AZD3480, the neuronal nicotinic receptor agent that we licensed from Targacept, Inc. in 2005, has successfully progressed into phase IIb clinical testing in both Alzheimer’s disease and cognitive disorders in schizophrenia (CDS). We have exercised a right to acquire an option from Targacept to take a licence of TC-5619, which Targacept is developing in CDS.

Back to top ↑