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                   236 records for 85 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 recruitingNCT02367040
Copanlisib and Rituximab in Relapsed Indolent B-cell Non-Hodgkin's Lymphoma (iNHL)
12/02/2015
Not recruitingNCT02282176
TINN2: Treat Infection in NeoNates 2
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2013-003889-14-HUTreat Infections in Neonates 211/12/2014
17/10/2014
RecruitingNCT02236637
A Registry to Observe the Treatment of Prostate Cancer Under Routine Medical Care
08/09/2014
RecruitingNCT02156804
A Single-Arm, Open-Label, Multicenter Clinical Trial With Nivolumab (BMS-936558) for Subjects With Histologically Confirmed Stage III (Unresectable) or Stage IV Melanoma Progressing Post Prior Treatment Containing an Anti-CTLA4 Monoclonal Antibody (CheckMate 172)
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2014-001286-28-ATA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.06/08/2014
AuthorisedEUCTR2014-001286-28-BEA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.23/07/2014
AuthorisedEUCTR2014-001286-28-ESA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.06/08/2014
AuthorisedEUCTR2014-001286-28-DEA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.01/08/2014
AuthorisedEUCTR2014-001286-28-NLA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.06/08/2014
AuthorisedEUCTR2014-001286-28-PTA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.29/08/2014
AuthorisedEUCTR2014-001286-28-SEA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.30/09/2014
AuthorisedEUCTR2014-001286-28-FIA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.17/10/2014
AuthorisedEUCTR2014-001286-28-DKA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.13/08/2014
AuthorisedEUCTR2014-001286-28-ITA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.31/07/2014
AuthorisedEUCTR2014-001286-28-IEA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.11/09/2014
AuthorisedEUCTR2014-001286-28-GBA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.04/08/2014
AuthorisedEUCTR2014-001286-28-HUA multicenter clinical study with Nivolumab for subjects with confirmed stage III or stage IV melanoma post treament with an Anti-CTLA-4 antibody.29/12/2014
Not RecruitingDRKS00006730A Single-Arm, Open-Label, Multicenter Clinical Trial With Nivolumab (BMS-936558) for Subjects With Histologically Confirmed Stage III (Unresectable) or Stage IV Melanoma Progressing Post Prior Treatment Containing an Anti-CTLA4 Monoclonal Antibody08/12/2014
29/05/2014
RecruitingNCT02149108
Nintedanib (BIBF 1120) vs Placebo in Refractory Colorectal Cancer
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2012-000095-42-SENintedanib (BIBF 1120) vs placebo in refractory colorectal cancer11/08/2014
AuthorisedEUCTR2012-000095-42-BENintedanib (BIBF 1120) vs placebo in refractory colorectal cancer25/08/2014
AuthorisedEUCTR2012-000095-42-NLNintedanib (BIBF 1120) vs placebo in refractory colorectal cancer28/08/2014
AuthorisedEUCTR2012-000095-42-DENintedanib (BIBF 1120) vs placebo in refractory colorectal cancer25/08/2014
AuthorisedEUCTR2012-000095-42-DKNintedanib (BIBF 1120) vs placebo in refractory colorectal cancer21/08/2014
AuthorisedEUCTR2012-000095-42-ATNintedanib (BIBF 1120) vs placebo in refractory colorectal cancer13/08/2014
AuthorisedEUCTR2012-000095-42-PLNintedanib (BIBF 1120) vs placebo in refractory colorectal cancer18/11/2014
AuthorisedEUCTR2012-000095-42-PTNintedanib (BIBF 1120) vs placebo in refractory colorectal cancer27/08/2014
26/05/2014
RecruitingNCT02141438
Observational Study for the Evaluation of Long-term Safety of Radium-223 Used for the Treatment of Metastatic Castration Resistant Prostate Cancer
Recruitment statusMain IDPublic titleDate of registration
RecruitingDRKS00006475Radium-223 Alpha Emitter Agent in Non-intervention Safety Study in mCRPC popUlation for Long-teRm Evaluation04/11/2014
15/05/2014
RecruitingDRKS00006153
QUIPS - Quality improvement in post operative pain treatment
12/05/2014
Not recruitingNCT02227758
Peripheral Nerve Stimulation Registry for Intractable Migraine Headache
Recruitment statusMain IDPublic titleDate of registration
RecruitingDRKS00007247Peripheral Nerve Stimulation Registry for Intractable Migraine Headache24/04/2015
16/04/2014
RecruitingNCT02138838
A Study to Assess the Efficacy and Safety of Cinacalcet in Pediatric Subjects With SHPT and CKD on Dialysis
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2013-004958-18-HUA Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis20/06/2014
AuthorisedEUCTR2013-004958-18-SKA Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis04/06/2014
Not AvailableEUCTR2013-004958-18-Outside-EU/EEAA Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis22/10/2014
AuthorisedEUCTR2013-004958-18-DEA Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis12/09/2014
AuthorisedEUCTR2013-004958-18-BEA Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis28/07/2014
AuthorisedEUCTR2013-004958-18-PTA Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis09/09/2014
AuthorisedEUCTR2013-004958-18-CZA Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis18/08/2014
01/04/2014
Not recruitingNCT02099409
Safety and Efficacy of Overnight Closed Loop in Children With Type 1Diabetes Mellitus in Luxembourg
26/03/2014
    
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