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Kusajili – Centralise les essais cliniques mondiaux
Résultat
de votre recherche par promoteur : AstraZeneca GmbH
Femme et Homme Max 99 ans
AstraZeneca GmbH
MAJ Il y a 4 ans
RACE : Rapid Dose Escalation of Quetiapine versus Conventional Escalation in the Treatment of Patients with Acute Schizophrenia – a Multicentre, Double-blind, Parallel group, Randomized Study
The primary objective for the study is to evaluate the safety and tolerability of IR (Immediate-Release) quetiapine in a rapid escalation scheme (300 mg on day 1, 600 mg on day 2 and 800 mg on day 3) ...
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Essai clos aux inclusions
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Femme Max 99 ans
AstraZeneca GmbH
MAJ Il y a 4 ans
Addition of vandetanib to standard therapy (pegliposomal doxorubicin) in patients with recurrent ovarian cancer. A multi-centre, non-randomized, open phase I/randomized phase II study
to evaluate the tolerability and safety of once daily oral Vandetanib 100 mg when added to standard therapy (pegliposomal doxorubicin 50 mg/m2 iv every 4 weeks) compared to standard therapy alone (peg...
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Essai clos aux inclusions
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Femme Max 99 ans
AstraZeneca GmbH
MAJ Il y a 4 ans
The Effect of the Atypical Antipsychotic Quetiapine in the Treatment of Postpartum Depressive Disorders with or without Psychotic Symptoms
The main (primary) objective of this study is to evaluate the efficacy of quetiapine in the treatment of postpartum depressive disorders in female patients with or without psychotic symptoms. The corr...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
AstraZeneca GmbH
MAJ Il y a 4 ans
A randomized, open, parallel-group, multi-centre, phase IV study to evaluate the efficacy of three different patient management strategies with and without esomeprazole 20 mg during a 3 months maintenance phase following an initial 4-weeks acute treatment phase in subjects with symptoms thought to be GERD related
To compare the efficacy of three different long-term treatment strategies in primary care setting, separately within different levels of symptom load according to clinical judgement at baseline (Visit...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
AstraZeneca GmbH
MAJ Il y a 4 ans
A One-Year Randomized, Prospective, Parallel, Open Comparison of Subjective Well-being in Schizophrenic Out-patients Treated with Quetiapine XR (SEROQUEL XR™) or Oral Risperidone at Flexible Dose in a Naturalistic Setting
The primary objective of this study is to demonstrate the non-inferiority of quetiapine XR to risperidone assessed at month 6 in terms of responder rate using the self-report instrument SWN-K.
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Essai clos aux inclusions
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