- Trials with a EudraCT protocol (28,525)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28,525 result(s) found for: - Crohn’s Disease.
Displaying page 737 of 1,427.
| EudraCT Number: 2015-001503-31 | Sponsor Protocol Number: RD.03.SPR.105078 | Start Date*: 2015-11-30 | |||||||||||
| Sponsor Name:Galderma R&D | |||||||||||||
| Full Title: Subject adherence and satisfaction for treatment of Onychomycosis with Loceryl® Nail Lacquer 5% versus Canesten® Fungal Nail Treatment Set | |||||||||||||
| Medical condition: Mycological confirmed toenail Distal and Lateral Subungual Onychomycosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IS (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001464-19 | Sponsor Protocol Number: GE-122-020 | Start Date*: 2016-02-11 | ||||||||||||||||
| Sponsor Name:GE Healthcare Ltd. and its affiliates | ||||||||||||||||||
| Full Title: AdreView™ Myocardial Imaging for Risk Evaluation – A multicentre trial to guide ICD implantation in NYHA class II & III heart failure patients with 30%≤LVEF≤35% ADMIRE-ICD | ||||||||||||||||||
| Medical condition: Heart failure | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-002996-12 | Sponsor Protocol Number: GS-US-367-1173 | Start Date*: 2016-02-16 | ||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
| Full Title: A Phase 3, Global, Multicenter, Randomized, Open-Label Study to Investigate the Safety and Efficacy of Sofosbuvir/Velpatasvir/GS-9857 Fixed-Dose Combination for 8 Weeks and Sofosbuvir/Velpatasvir f... | ||||||||||||||||||
| Medical condition: Chronic Hepatitis C virus infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) GB (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-001677-16 | Sponsor Protocol Number: RD.03.SPR.104003 | Start Date*: 2018-04-05 | |||||||||||
| Sponsor Name:Galderma S.A. | |||||||||||||
| Full Title: A randomized, double-blind, multi-centre, placebo-controlled, parallel-arm phase 2 trial to assess safety, efficacy and pharmacokinetics of CD11301 0.03% and 0.06% gel in the treatment of Cutaneous... | |||||||||||||
| Medical condition: Cutaneous T Cell Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003113-17 | Sponsor Protocol Number: MEU17/361 | Start Date*: 2018-11-09 | |||||||||||
| Sponsor Name:The Medicines Evaluation Unit (MEU) Ltd. (Investigator led study) | |||||||||||||
| Full Title: A randomised, open label 2-way cross-over study to compare the effects of inhaled Beclometasone/Formoterol/Glycopyrronium (TRIMBOW) pMDI to Beclometasone/Formoterol (FOSTAIR) pMDI on hyperinflation... | |||||||||||||
| Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003792-63 | Sponsor Protocol Number: UCL/17/0629 | Start Date*: 2018-10-23 | ||||||||||||||||
| Sponsor Name:University College London | ||||||||||||||||||
| Full Title: Phase II trial of maintenance pembrolizumab following weekly paclitaxel for recurrent ovarian, fallopian tube or peritoneal cancer | ||||||||||||||||||
| Medical condition: recurrent ovarian/fallopian tube or primary non-mucinous peritoneal cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-002589-37 | Sponsor Protocol Number: SL0008 | Start Date*: 2008-07-17 | |||||||||||
| Sponsor Name:UCB Inc | |||||||||||||
| Full Title: A Phase IIb, Multi-center, Open-label, Follow-up Study to Assess the Safety and Efficacy of Epratuzumab in Serologically-positive Systemic Lupus Erythematosus Patients with Active Disease Who Parti... | |||||||||||||
| Medical condition: systemic lupus erythematosus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) LT (Completed) HU (Completed) BE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-018565-26 | Sponsor Protocol Number: SL0010 | Start Date*: 2011-01-16 | |||||||||||
| Sponsor Name:UCB Inc. | |||||||||||||
| Full Title: A phase 3, randomized, double-blind, placebo-controlled, multicenter study of the efficacy and safety of four 12-week treatment cycles (48 weeks total) of Epratuzumab in systemic lupus erythematosu... | |||||||||||||
| Medical condition: Systemic Lupus Erythmatosus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Completed) DE (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021886-63 | Sponsor Protocol Number: RD2010-48 | Start Date*: 2011-07-14 | |||||||||||
| Sponsor Name:East and North Hertfordshire NHS Trust [...] | |||||||||||||
| Full Title: A trial of Prostate Radiotherapy in Conjunction with Carbogen and Nicotinamide (PROCON) | |||||||||||||
| Medical condition: Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-001987-24 | Sponsor Protocol Number: D3820C00004 | Start Date*: 2011-08-22 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of NKTR-118 in Patients with Non-Cancer-Related Pain and Opioid-Induced Constipation (OIC) | |||||||||||||
| Medical condition: Opioid-induced constipation (OIC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001735-22 | Sponsor Protocol Number: CNTO328SMM2001 | Start Date*: 2011-09-28 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Multicenter Study of Siltuximab (Anti IL 6 Monoclonal Antibody) in Subjects with High-risk Smoldering Multiple Myeloma | |||||||||||||
| Medical condition: High-risk Smoldering Multiple Myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) SE (Completed) FR (Completed) GR (Completed) ES (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004631-31 | Sponsor Protocol Number: REM-PH-416 | Start Date*: 2012-03-13 | |||||||||||||||||||||
| Sponsor Name:United Therapeutics Corp. | |||||||||||||||||||||||
| Full Title: A 16 Week, Open Label, Multi-Centre, Study to Evaluate the Safety, Tolerability and Pharmacodynamic Effects of a Rapid Dose Titration Regimen of Subcutaneous Remodulin® Therapy in Subjects with Pul... | |||||||||||||||||||||||
| Medical condition: Pulmonary Arterial Hypertension (PAH) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-002545-35 | Sponsor Protocol Number: OCTO_026 | Start Date*: 2012-01-23 | |||||||||||
| Sponsor Name:University of Oxford | |||||||||||||
| Full Title: A randomised phase 2 study of paclitaxel with or without GSK1120212 in advanced wt BRAF melanoma | |||||||||||||
| Medical condition: Advanced/metastatic melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003141-16 | Sponsor Protocol Number: HEM2012BL01 | Start Date*: 2012-10-18 | |||||||||||
| Sponsor Name:VU University Medical Center | |||||||||||||
| Full Title: Efficacy and feasibility of first-line treatment with risk-adapted dose-adjusted EPOCH-R (DA-EPOCH-R) in patients with Burkitt lymphoma. A phase II clinical trial. | |||||||||||||
| Medical condition: Burkitt lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003510-13 | Sponsor Protocol Number: IRST174.08 | Start Date*: 2013-05-07 | |||||||||||
| Sponsor Name:IRCCS ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI | |||||||||||||
| Full Title: A phase II non randomized study evaluating the role of Androgen Receptors as Targets for therapy of pre-treated post-menopausal patients with ER/PgR-negative/AR-positive or ER and/or PgR-positive/A... | |||||||||||||
| Medical condition: pre-treated post-menopausal patients with ER/PgR-negative/AR-positive or ER and/or PgR-positive/AR-positive metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003545-41 | Sponsor Protocol Number: D1344C00001 | Start Date*: 2014-04-14 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Randomised, Double-Blind Study to Assess the Efficacy of Selumetinib (AZD6244, Hyd-Sulfate) in Combination with Dacarbazine Compared with Placebo in Combination with Dacarbazine as First Systemic... | |||||||||||||
| Medical condition: Metastatic uveal melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) CZ (Completed) DE (Completed) NL (Completed) FI (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000242-30 | Sponsor Protocol Number: CNTO148PSA3001 | Start Date*: 2014-12-29 | |||||||||||
| Sponsor Name:Janssen Biologics, BV | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled Trial of Golimumab, an Anti-TNFα Monoclonal Antibody, Administered Intravenously, in Subjects with Active Psoriatic Arthritis | |||||||||||||
| Medical condition: Psoriatic Arthritis (PsA) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) LT (Completed) ES (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013408-30 | Sponsor Protocol Number: 2009-013408-30 | Start Date*: 2010-08-23 | |||||||||||||||||||||
| Sponsor Name:University College London | |||||||||||||||||||||||
| Full Title: Randomised phase II trial of cediranib (AZD2171) vs. placebo in addition to cisplatin / gemcitabine chemotherapy for patients with advanced biliary tract cancers | |||||||||||||||||||||||
| Medical condition: biliary tract carcinomas (including gallbladder cancer and cholangiocarcinomas) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-003167-10 | Sponsor Protocol Number: GS-US-367-1170 | Start Date*: 2016-02-16 | ||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
| Full Title: A Phase 3, Global, Multicenter, Randomized, Open-Label Study to Investigate the Safety and Efficacy of Sofosbuvir/Velpatasvir/GS-9857 Fixed-Dose Combination for 12 Weeks and Sofosbuvir/Velpatasvir ... | ||||||||||||||||||
| Medical condition: Chronic Hepatitis C virus infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) FR (Completed) GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-001356-22 | Sponsor Protocol Number: CLR_09_21 | Start Date*: 2016-07-13 | |||||||||||
| Sponsor Name:Sun Pharma Advanced Research Company Ltd. | |||||||||||||
| Full Title: A PLACEBO-CONTROLLED RANDOMIZED WITHDRAWAL EVALUATION OF THE EFFICACY AND SAFETY OF BACLOFEN ER CAPSULES (GRS) IN SUBJECTS WITH SPASTICITY DUE TO MULTIPLE SCLEROSIS | |||||||||||||
| Medical condition: Spasticity due to multiple sclerosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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