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Kusajili – Clinical trials directory
Result
of your search per sponsor: AstraZeneca AB
Woman and Man Max 99 years
AstraZeneca AB; Karlebyhus, Astraallén, Södertälje SE-151 85, Sweden
Update Il y a 4 ans
A randomised, double blind, placebo controlled, parallel study to assess the benefits of aclidinium bromide in the relief of COPD (Chronic obstructive pulmonary disease) symptoms including cough when administered to patients with COPD
1. To assess the effect of aclidinium bromide 400 µg administered twice a day on COPD symptoms including cough in patients with moderate COPD compared to placebo. 2. To assess the effects of aclidin...
Country
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organs
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Specialty
None
Closed trial
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Woman and Man Max 99 years
AstraZeneca AB
Update Il y a 4 ans
A 4-week, Double-Blind, Placebo-Controlled, Randomised, Parallel group, Multi-Centre, Phase IIa Study to Investigate the Tolerability and Safety of 100 mg Oral AZD2423 in Patients with Moderate to Severe COPD
To investigate the tolerability and safety of AZD2423 in patients with COPD
Country
None
organs
None
Specialty
None
Closed trial
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Woman Max 99 years
AstraZeneca AB
Update Il y a 4 ans
An Open Label, Single Arm, Multicentre Study of Lynparza (Olaparib) Capsules in Relapsed BRCA Mutated Ovarian Cancer Patients (ORZORA)
To assess the real world clinical effectiveness of olaparib maintenance monotherapy by investigator assessed progression free survival (PFS) according to modified Response Evaluation Criteria In Solid...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
AstraZeneca AB
Update Il y a 4 ans
A 52-Week International, Multi-centre, Randomised, Parallel-group, Double-blind, Active-controlled, Phase III study with a 52-Week Extension Period to Evaluate the Safety and Efficacy of Saxagliptin in Combination with Metformin compared with Sulphonylurea in Combination with Metformin in Adult Patients with Type 2 Diabetes who have Inadequate Glycaemic Control on Metformin Therapy Alone
To compare that after 52-week oral administration of double-blind treatment, the absolute change from baseline in glycosylated haemoglobin A1c (HBA1c) level with saxagliptin plus metformin is non-inf...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
AstraZeneca AB
Update Il y a 4 ans
A late stage clinical trial to investigate the efficacy and safety of AZD9291 versus Placebo in patients with stage IB-IIIA non-small cell lung carcinoma, following complete tumour resection with or without adjuvant chemotherapy
To assess the efficacy of AZD9291 compared to placebo as measured by disease free survival (DFS)
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
AstraZeneca AB
Update Il y a 4 ans
A 52-week, double-blind, randomised, multi-centre, phase III, parallel-group study in patients 12 years and older with asthma, evaluating the efficacy and safety of Symbicort (budesonide/formoterol) Turbuhaler 160/4.5 μg ‘as needed’ compared with Pulmicort (budesonide) Turbuhaler 200 μg twice daily plus terbutaline Turbuhaler 0.4 mg ‘as needed’
To demonstrate that Symbicort Turbuhaler 160/4.5 μg ‘as needed’ is non-inferior to Pulmicort Turbuhaler 200 μg twice daily plus terbutaline Turbuhaler 0.4 mg ‘as needed’
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
AstraZeneca AB
Update Il y a 4 ans
A Phase II, double-blind, randomized, cross-over, international, multicentre study to evaluate the analgesic efficacy of 3 weeks oral administration of AZD4282 300 mg b.i.d. compared with placebo in postherpetic neuralgia
To evaluate the analgesic efficacy of 3 weeks oral administration of AZD4282 compared with placebo in postherpetic neuralgia.
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
AstraZeneca AB
Update Il y a 4 ans
A 4-week, phase-II, double-blind, placebo-controlled, randomized, parallel group, multi-centre study to assess the efficacy and tolerability/safety of inhaled AZD3199 once daily compared to 9 μg formoterol bid and placebo in patients with moderate to severe COPD
Primary objective is: • To compare the clinical efficacy of AZD3199 inhaled once daily with 9 μg formoterol twice daily and placebo over a 4-week treatment period in adults with chronic obstructive pu...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
AstraZeneca AB
Update Il y a 4 ans
A phase II, double-blind, placebo-controlled, randomised, 6-way cross-over, single-dose study to investigate the local and systemic effects of 3 doses of inhaled AZD3199 (a β2-agonist) compared to formoterol in asthmatic patients
The primary objective of the study is to investigate the pharmacodynamics of AZD3199 inhaled via Turbuhaler compared to placebo and inhaled formoterol. The primary variable for local pulmonary effec...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
AstraZeneca AB
Update Il y a 4 ans
A Phase II, Randomised, Factorial, Double-blind Study to Investigate the Management of AZD2171-induced Hypertension and Efficacy of AZD2171 at Doses of 30 mg and 45 mg in Patients with Advanced Solid Tumours
In order to investigate the hypothesis that withdrawal of AZD2171 can be avoided by controlled anti-hypertensive therapy, the primary objective of the study is to identify a treatment strategy, consis...
Country
None
organs
None
Specialty
None
Closed trial
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