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format_facet:"Elektronische Ressource"
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publishDate:"[2010 TO 2019]"
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PubPharm (31.276)
1
A Study in Patients with Chronic Cluster Headache : A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study of LY2951742 with a Long-Term Open-Label Extension in Patients with Chronic Cluster Headache - I5Q-MC-CGAM
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| 2019
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2
Efficacy, Safety, and Tolerability of Fosmetpantotenate in patients with Pantothenate Kinase-associated Neurodegeneration (PKAN) : Efficacy, Safety, and Tolerability of Fosmetpantotenate (RE-024), a Phosphopantothenate replacement therapy, in patients with Pantothenate Kinase-associated Neurodegeneration (PKAN): A Randomized, Double-blind, Placebo-Controlled Study with an Open-Label Extension
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| 2019
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3
A Phase 3 Study to Compare the Efficacy and Safety of CT-P6 and Herceptin as Neoadjuvant and Adjuvant Treatment in Patients with HER2-Positive Early Breast Cancer : A Phase 3, Double-Blind, Randomized, Parallel-Group, Active-Controlled Study to Compare the Efficacy and Safety of CT-P6 and Herceptin as Neoadjuvant and Adjuvant Treatment in Patients with HER2-Positive Early Breast Cancer
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| 2019
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4
A phase 3 trial to evaluate the efficacy and safety of tralokinumab in combination with topical corticosteroid in adults with moderate to severe atopic dermatitis. ECZTRA 3 (ECZema TRAlokinumab trial no. 3) : A randomised, double-blind, placebo-controlled, phase 3 trial to evaluate the efficacy and safety of tralokinumab in combination with topical corticosteroid in subjects with moderate-to-severe atopic dermatitis who are candidates for systemic therapy - ECZTRA 3
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| 2019
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5
A double-masked study of SYL1001 in patients with moderate to severe dry eye disease : A double-masked study of SYL1001 in patients with moderate to severe dry eye disease (DED)
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| 2019
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6
This study will test an experimental drug called GS-9883/F/TAF (GS-9883/emtricitabine/tenofovir alafenamide) fixed dose combination (FDC) for the treatment of HIV-1 infection. The purpose of this study is to test the effectiveness of switching to GS-9883/F/TAF FDC versus continuing on DTG and ABC/3TC as the FDC ABC/DTG/3TC in HIV-1 infected adults who are virologically suppressed (HIV-1 RNA test <50 copies/mL) : A Phase 3, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of Switching from a Regimen of Dolutegravir and ABC/3TC, or a Fixed Dose Combination (FDC) of ABC/DTG/3TC to a FDC of GS-9883/F/TAF in HIV-1 Infected Subjects who are Virologically Suppressed
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| 2019
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7
A Study of Ibrutinib in Combination with Bendamustine and Rituximab in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma. : Randomized, Double-blind, Placebo-controlled Phase 3 Study of Ibrutinib, a Bruton's Tyrosine Kinase (BTK) Inhibitor, in Combination with Bendamustine and Rituximab (BR) in Subjects With Relapsed or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma.
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| 2019
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8
This study is being done to test the effectiveness and safety of an investigational drug called acalabrutinib (ACP-196) when taken with already marketed drugs called Venetoclax and Obinutzumab in comparison to chemotherapy that is already in wide use for treatment of patients who have chronic lymphocytic leukemia and who have never been treated before. : A Randomized, Multicenter, Open-Label, Phase 3 Study to Compare the Efficacy and Safety of Acalabrutinib (ACP-196) in Combination with Venetoclax with and without Obinutuzumab Compared to Investigator’s Choice of Chemoimmunotherapy in Subjects with Previously Untreated Chronic Lymphocytic Leukemia Without del(17p) or TP53 Mutation - Not available at this time
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| 2019
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9
An Efficacy and Safety Study of Alirocumab in Children and Adolescents with Heterozygous Familial Hypercholesterolemia : A Randomized, Double-Blind, Placebo-Controlled Study Followed by an Open Label Treatment Period to Evaluate the Efficacy and Safety of Alirocumab in Children and Adolescents with Heterozygous Familial Hypercholesterolemia
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| 2019
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10
VACCINATION ADJUVED AGAINST HEPATITIS B IN SACYL WORKERS TYPED AS NO RESPONDERS TO CONVENTIONAL VACCINES : VACCINATION ADJUVED AGAINST HEPATITIS B IN SACYL WORKERS TYPED AS NO RESPONDERS TO CONVENTIONAL VACCINES
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| 2019
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Medienart: E-Ressourcen
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Thema: Phase: Phase 3
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Erscheinungsjahr: 2010-2019
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31.276
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31.276
WHO International Clinical Trials Registry Plat...
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Phase: Phase 3
31.148
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Recruitment Status: Authorised-recruitment may ...
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Study Type: Observational
68
Medical Condition: Acute heart failure;Therapeu...
68
Medical Condition: Asthma MedDRA version: 20.0 ...
62
Medical Condition: ;Neoplasms
54
Medical Condition: Asthma MedDRA version: 20.0L...
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Medical Condition: Asthma MedDRA version: 18.1L...
44
Medical Condition: ;Endocrine, nutritional and ...
44
Medical Condition: ;Not Applicable
40
Medical Condition: ;Diseases of the digestive s...
38
Medical Condition: Hypertension
34
Medical Condition: Active Crohn's disease MedDR...
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Medical Condition: Diabetes Mellitus, Type 2 Me...
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Medical Condition: ;Diseases of the blood and b...
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2010-2019
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