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                   1350 records for 323 trials found!
Trials are sometimes recorded in more than one registry. These records can refer to each other using the 'Secondary ID' field. The search portal uses these Secondary IDs to group records about the same trial together in the search results.
Each group of records referring to a trial is displayed in table that is seen by pressing the + symbol. The record with the earliest date of registration is always shown first.
 
 
 
 
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Recruitment statusMain ID Public TitleDate of Registration
Not recruitingNCT02567006
SMS Mobile Technology to Improve Early Childhood Vaccine Coverage in Guatemala
30/09/2015
Not recruitingNCT02563054
A Study of Capecitabine (Xeloda) in Participants With Advanced or Metastatic Gastric Cancer
28/09/2015
AuthorisedEUCTR2014-002208-26-NO
Study to assess the efficacy and safety of a new contraceptive vaginal ring containing etonogestrel and estradiol and a marketed oral contraceptive pill containing levonorgestrel and ethinyl-estradiol.
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2014-002208-26-NLStudy to assess the efficacy and safety of a new contraceptive vaginal ring containing etonogestrel and estradiol and a marketed oral contraceptive pill containing levonorgestrel and ethinyl-estradiol.20/10/2015
AuthorisedEUCTR2014-002208-26-FIStudy to assess the efficacy and safety of a new contraceptive vaginal ring containing etonogestrel and estradiol and a marketed oral contraceptive pill containing levonorgestrel and ethinyl-estradiol.15/09/2015
AuthorisedEUCTR2014-002208-26-ESStudy to assess the efficacy and safety of a new contraceptive vaginal ring containing etonogestrel and estradiol and a marketed oral contraceptive pill containing levonorgestrel and ethinyl-estradiol.13/10/2015
AuthorisedEUCTR2014-002208-26-DEStudy to assess the efficacy and safety of a new contraceptive vaginal ring containing etonogestrel and estradiol and a marketed oral contraceptive pill containing levonorgestrel and ethinyl-estradiol.07/09/2015
AuthorisedEUCTR2014-002208-26-HUStudy to assess the efficacy and safety of a new contraceptive vaginal ring containing etonogestrel and estradiol and a marketed oral contraceptive pill containing levonorgestrel and ethinyl-estradiol.22/10/2015
AuthorisedEUCTR2014-002208-26-SEStudy to assess the efficacy and safety of a new contraceptive vaginal ring containing etonogestrel and estradiol and a marketed oral contraceptive pill containing levonorgestrel and ethinyl-estradiol.27/08/2015
26/08/2015
AuthorisedEUCTR2015-001020-27-DE
A Study of Single Agent Pembrolizumab versus Single Agent Chemotherapy for Metastatic Triple Negative Breast Cancer. 20/08/2015
AuthorisedEUCTR2015-000114-22-EE
Evaluation of the efficacy and safety of QVA149 (110/50 µg o.d.) vs tiotropium (18 µg o.d.) + salmeterol/fluticasone propionate FDC (50/500 µg b.i.d.) in patients with moderate to severe COPD
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2015-000114-22-LVEvaluation of the efficacy and safety of QVA149 (110/50 µg o.d.) vs tiotropium (18 µg o.d.) + salmeterol/fluticasone propionate FDC (50/500 µg b.i.d.) in patients with moderate to severe COPD27/08/2015
AuthorisedEUCTR2015-000114-22-HUEvaluation of the efficacy and safety of QVA149 (110/50 µg o.d.) vs tiotropium (18 µg o.d.) + salmeterol/fluticasone propionate FDC (50/500 µg b.i.d.) in patients with moderate to severe COPD16/09/2015
AuthorisedEUCTR2015-000114-22-ESEvaluation of the efficacy and safety of QVA149 (110/50 ?g o.d.) vs tiotropium (18 ?g o.d.) + salmeterol/fluticasone propionate FDC (50/500 ?g b.i.d.) in patients with moderate to severe COPD30/10/2015
AuthorisedEUCTR2015-000114-22-LTEvaluation of the efficacy and safety of QVA149 (110/50 µg o.d.) vs tiotropium (18 µg o.d.) + salmeterol/fluticasone propionate FDC (50/500 µg b.i.d.) in patients with moderate to severe COPD31/08/2015
AuthorisedEUCTR2015-000114-22-ATEvaluation of the efficacy and safety of QVA149 (110/50 µg o.d.) vs tiotropium (18 µg o.d.) + salmeterol/fluticasone propionate FDC (50/500 µg b.i.d.) in patients with moderate to severe COPD05/11/2015
AuthorisedEUCTR2015-000114-22-SKEvaluation of the efficacy and safety of QVA149 (110/50 µg o.d.) vs tiotropium (18 µg o.d.) + salmeterol/fluticasone propionate FDC (50/500 µg b.i.d.) in patients with moderate to severe COPD22/09/2015
RecruitingNCT02603393Evaluation of the Efficacy and Safety of QVA149 (110/50 µg o.d.) vs Tiotropium (18 µg o.d.) + Salmeterol/Fluticasone Propionate FDC (50/500 µg b.i.d.) in Patients With Moderate to Severe COPD17/09/2015
AuthorisedEUCTR2015-000114-22-DEEvaluation of the efficacy and safety of QVA149 (110/50 µg o.d.) vs tiotropium (18 µg o.d.) + salmeterol/fluticasone propionate FDC (50/500 µg b.i.d.) in patients with moderate to severe COPD10/09/2015
AuthorisedEUCTR2015-000114-22-HREvaluation of the efficacy and safety of QVA149 (110/50 µg o.d.) vs tiotropium (18 µg o.d.) + salmeterol/fluticasone propionate FDC (50/500 µg b.i.d.) in patients with moderate to severe COPD01/02/2016
11/08/2015
RecruitingNCT02509936
Promoting Physical Growth and Positive Development in Severely Stunted Guatemalan Children
17/07/2015
AuthorisedEUCTR2015-000972-88-LT
Ph III Trial of Pembrolizumab (MK-3475), pembrolizumab+FP/XP vs. Placebo+FP/XP in Biomarker Select, Advanced Gastric or GEJ Adenocarcinoma
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2015-000972-88-NLPh III Trial of Pembrolizumab (MK-3475), pembrolizumab+FP/XP vs. Placebo+FP/XP in Biomarker Select, Advanced Gastric or GEJ Adenocarcinoma07/07/2015
AuthorisedEUCTR2015-000972-88-HUPh III Trial of Pembrolizumab (MK-3475), pembrolizumab+FP/XP vs. Placebo+FP/XP in Biomarker Select, Advanced Gastric or GEJ Adenocarcinoma13/08/2015
AuthorisedEUCTR2015-000972-88-LVPh III Trial of Pembrolizumab (MK-3475), pembrolizumab+FP/XP vs. Placebo+FP/XP in Biomarker Select, Advanced Gastric or GEJ Adenocarcinoma30/06/2015
AuthorisedEUCTR2015-000972-88-ESPh III Trial of Pembrolizumab (MK-3475), pembrolizumab+FP/XP vs. Placebo+FP/XP in Biomarker Select, Advanced Gastric or GEJ Adenocarcinoma10/07/2015
AuthorisedEUCTR2015-000972-88-ATPh III Trial of Pembrolizumab (MK-3475), pembrolizumab+FP/XP vs. Placebo+FP/XP in Biomarker Select, Advanced Gastric or GEJ Adenocarcinoma07/08/2015
AuthorisedEUCTR2015-000972-88-PLPh III Trial of Pembrolizumab (MK-3475), pembrolizumab+FP/XP vs. Placebo+FP/XP in Biomarker Select, Advanced Gastric or GEJ Adenocarcinoma01/10/2015
RecruitingNCT02494583Study of Pembrolizumab (MK-3475) as First-Line Monotherapy and Combination Therapy for Treatment of Advanced Gastric or Gastroesophageal Junction Adenocarcinoma (MK-3475-062/KEYNOTE-062)08/07/2015
AuthorisedEUCTR2015-000972-88-CZPh III Trial of Pembrolizumab (MK-3475), pembrolizumab+FP/XP vs. Placebo+FP/XP in Biomarker Select, Advanced Gastric or GEJ Adenocarcinoma31/07/2015
26/06/2015
RecruitingNCT02486237
Complications in Central American Diabetic Patients: Historic Cohort
22/06/2015
AuthorisedEUCTR2014-005663-32-LV
Study of efficacy and safety of secukinumab in pediatric patients with severe plaque psoriasis. 12/06/2015
AuthorisedEUCTR2014-002807-10-DE
Pediatric PK Study (POS IV and PFS)
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2014-002807-10-ESPediatric PK Study (POS IV and PFS)15/06/2015
AuthorisedEUCTR2014-002807-10-SEPediatric PK Study (POS IV and PFS)19/05/2015
AuthorisedEUCTR2014-002807-10-CZPediatric PK Study (POS IV and PFS)08/06/2015
RecruitingNCT02452034Safety and Pharmacokinetics of Intravenous and Oral Posaconazole in Immunocompromised Children (MK-5592-097)20/05/2015
13/05/2015
    
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