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4052 Results:

Sponsor	Study ID ↑	Description	Created

Astellas	*ASTELLAS-9463-EC-0002	An Exploratory Study to Compare the Efficacy and Safety of Micafungin as a Pre-emptive Treatment of Invasive Candidiasis Versus Placebo in High Risk Surgical Subjects with Intra-abdominal Infections - A Multicentre, Randomized, Double-blind Study	7/31/2017

Bayer	*BAYER-B078	Five-year Clinical Performance of the New Formulation of the Levonorgestrel Intrauterine System and Serum Levonorgestrel Concentration with the New Formulation Compared to That with the Original One. Medicine: Levonorgestrel, Condition: Contraception, Phase: 3, Clinical Study ID: B078, Sponsor: Bayer	11/30/2016

Boehringer Ingelheim	*BI-1123.10	Full Dose Tenecteplase (TNK-tPA) Together With Heparin Sodium, Full Dose Tenecteplase With Enoxaparin, Half Dose Tenecteplase Together With Abciximab and Heparin Sodium in Patients With Acute Myocardial Infarction (AMI)	9/30/2014

Boehringer Ingelheim	*BI-1123.11	A Trial on Efficacy and Safety of Full Dose Tenecteplase Combined With Unfractionated Heparin (UFH) or Enoxaparin in Acute Myocardial Infarction (AMI) in the Prehospital Setting	9/30/2014

Boehringer Ingelheim	*BI-1123.12	A Trial Evaluating the Efficacy and Safety of Tenecteplase Together With Unfractionated Heparin Prior to Early Percutaneous Coronary Intervention (PCI) as Compared to Standard Primary PCI in Patients With Acute Myocardial Infarction (ASSENT 4 PCI)	9/30/2014

Boehringer Ingelheim	*BI-1123.18	Thrombolysis Using Tenecteplase (Metalyse®) in Cardiac Arrest - The TROICA Trial	9/30/2014

Boehringer Ingelheim	*BI-1123.28	STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction	10/26/2015

Boehringer Ingelheim	*BI-1123.8	Trial to Compare the Efficacy and Safety of a Single Bolus of TNK-tPA (Tenecteplase, Metalyse®) With Accelerated Infusion of Rt-PA (Alteplase, Actilyse®) in Asian Patients With Acute Myocardial Infarction	10/26/2015

Boehringer Ingelheim	*BI-1208.10	Study to Evaluate the Efficacy of Duloxetine in Outpatients With Major Depressive Disorder and Pain	1/2/2015

Boehringer Ingelheim	*BI-1208.22	A double-blind, stratified, randomised, parallel, placebo-controlled, multi-centre study to assess the efficacy and safety of duloxetine (20 mg bid for 2 weeks escalating to 40 mg bid) for up to 12 weeks, compared to placebo, in community-dwelling elderly women >= 65 years of age with symptoms of stress urinary incontinence or stress-predominant mixed urinary incontinence	1/2/2015

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