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  • All Diseases and Conditions

The following clinical trials are associated with All diseases and conditions.

There are a number of ways to help you find trial information.  By using these filters you can find (i) recruiting status, (ii) therapy area, (iii) product and/or (iv) phase of drug development.  You can use one or all filters to identify your specific needs.

When a trial completes the results are reported here no later than one year after completion – this is why you may sometimes find that a Report is unavailable when you are searching through ‘closed’ trials.

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  • expand Drug utilization and safety events among children using esomeprazole, other proton pump inhibitors or H2-receptor antagonists
    Study Id
    D9612N00016
    Disease
    gastroesophageal reflux disease
    Drug Name
    Nexium
    Study Name
    D9612N00016
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand A Phase I, Randomized, Double-Blind, Placebo-Controlled, Two-Part, Multiple Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics and Effect on Biomarkers of AZD3293 in Plasma and Cerebrospinal Fluid in Healthy Male and Non-Fertile Female Elderly Volunteers and in Mild-to-Moderate Alzheimer Disease Patients.
    Study Id
    D5010C00002
    Disease
    Alzheimer's Disease
    Drug Name
    AstraZeneca Neuroscience Development Drugs
    Study Name
    D5010C00002
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand Observational retrospective Study to Describe the Management of Advanced or Metastatic EGFR Mutated Non-small Cell Lung Cancer Patients in Spain.
    Study Id
    NIS-OES-XXX-2012/1
    Disease
    non-small cell lung cancer
    Drug Name
    non drug study (oncology)
    Study Name
    NIS-OES-XXX-2012/1
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand A Phase III, Randomized, Multicenter, Double Blind, Double-Dummy, Parallel-Group, Comparative Study to Determine the Efficacy, Safety, and Tolerability of Ceftazidime Avibactam Plus Metronidazole Versus Meropenem in the Treatment of Complicated Intra-Abdominal Infections In Hospitalized Adults
    Study Id
    D4280C00018
    Disease
    infection
    Drug Name
    CAZ-104
    Study Name
    RECLAIM3
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand A diagnostic study to determine the prevalence of EGFR mutations in Asian and Russian patients with advanced NSCLC of Adenocarcinoma and Non-adenocarcinoma histologies
    Study Id
    D7913C00074
    Disease
    non-small cell lung cancer
    Drug Name
    non drug study (oncology)
    Study Name
    D7913C00074
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand Tolerability,Pharmacokinetics&Preliminary Antitumour Activity of Ascending Doses of AZD9291 in Patients With Advanced Non Small Cell LungCancer Who Have Progressed Following Prior Therapy With an Epidermal Growth FactorReceptorTyrosineKinaseInhibatoragent
    Study Id
    D5160C00001
    Disease
    non-small cell lung cancer
    Study Name
    D5160C00001
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand A Treatment With Fulvestrant and Exemestane in Postmenopausal Patients With Advanced Hormone Receptor-Positive (HR) + Breast Cancer (ACT-FASTER:)
    Study Id
    NIS-ODE-FAS-2009/1
    Disease
    advanced breast cancer
    Drug Name
    Faslodex
    Study Name
    NIS-ODE-FAS-2009/1
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand D1691C00007
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand D0490C00005
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
  • expand A multi-center, randomised, double-blind, parallel-group phase III study to assess high dose esomeprazole Na i.v. treatment (bolus infusion of 80 mg followed by a continuous infusion of 8 mg per hour administered for 72 hours) for prevention of rebleeding.
    Study Id
    D961DC00007
    Disease
    gastrointestinal bleeding, peptic ulcer
    Drug Name
    AstraZeneca Gastrointestinal Brands
    Study Name
    D961DC00007
    Recruiting Status
    Open
    Protocol Status
    Not Available
    Report Status
    Not Available
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