- Trials with a EudraCT protocol (11,933)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (909)
11,933 result(s) found for: II.
Displaying page 57 of 597.
| EudraCT Number: 2008-005479-82 | Sponsor Protocol Number: CACZ885G2301 | Start Date*: 2009-06-12 | |||||||||||
| Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||
| Full Title: Estudio doble ciego, randomizado, controlado con placebo, con diseño de retirada en la prevención de brotes con canakinumab (ACZ885) en pacientes con artritis idiopática juvenil sistémica y manifes... | |||||||||||||
| Medical condition: Artritis idiopática juvenil sistémica y manifestaciones sistémicas activas. | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) NO (Ongoing) FR (Completed) HU (Completed) BE (Completed) DE (Completed) SE (Completed) IT (Completed) GB (Completed) DK (Prematurely Ended) AT (Completed) GR (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002646-16 | Sponsor Protocol Number: 17000139BLC2001 | Start Date*: 2021-04-26 | ||||||||||||||||||||||||||
| Sponsor Name:Janssen-Cilag International NV | ||||||||||||||||||||||||||||
| Full Title: Phase 2b Clinical Study Evaluating Efficacy and Safety of TAR-200 in Combination with Cetrelimab, TAR-200 Alone, or Cetrelimab Alone in Participants with High-Risk Non-Muscle Invasive Bladder Cance... | ||||||||||||||||||||||||||||
| Medical condition: Non-Muscle-Invasive Urothelial Carcinoma (NMIBC) of the Bladder | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) PT (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-002892-30 | Sponsor Protocol Number: 1315.2 | Start Date*: 2016-04-14 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: An open-label, Phase I/II trial to determine the maximum tolerated dose and investigate safety, pharmacokinetics and efficacy of BI 836858 in combination with decitabine in patients with acute myel... | |||||||||||||
| Medical condition: patients with acute myeloid leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Ongoing) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004777-10 | Sponsor Protocol Number: 107240 | Start Date*: 2007-03-14 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A Phase I/II study to assess the safety and immunogenicity of recMAGE-A3+AS15 cancer immunotherapeutic given as adjuvant therapy, with or without standard adjuvant chemo(-radio)therapy, to patients... | ||
| Medical condition: Adult patients with pathologically proven MAGE A3-positive Non-Small Cell Lung Cancer in stage IB, II or III. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) BE (Prematurely Ended) DE (Completed) FR (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-000449-21 | Sponsor Protocol Number: CLAG525X2101C | Start Date*: 2015-08-31 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A Phase I/II, open label, multicenter study of the safety and efficacy of LAG525 single agent and in combination with PDR001 administered to patients with advanced malignancies | |||||||||||||
| Medical condition: Solid tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Completed) DE (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003407-18 | Sponsor Protocol Number: NN1436-4466 | Start Date*: 2019-04-04 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A trial comparing NNC0148-0287 C (insulin 287) versus insulin glargine U100, both in combination with metformin, with or without DPP4 inhibitors and with or without SGLT2 inhibitors, in basal ins... | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-005969-18 | Sponsor Protocol Number: CLAF237A23122 | Start Date*: 2007-03-27 | |||||||||||
| Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
| Full Title: Estudio multicéntrico, doble ciego, aleatorizado, de grupos paralelos para demostrar el efecto de 12 semanas de tratamiento con una combinación inicial 100 mg de Vildagliptina qd y 1.000 mg de metf... | |||||||||||||
| Medical condition: Diabetes Type II | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) HU (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002642-23 | Sponsor Protocol Number: NVD-CLN01 | Start Date*: 2016-11-28 |
| Sponsor Name:Novadip Biosciences | ||
| Full Title: A prospective multi-centre, randomised, controlled study to evaluate the safety and preliminary effectiveness of NVD-001 for the treatment of low grade degenerative lumbar spondylolisthesis by inte... | ||
| Medical condition: Patients diagnosed with symptomatic degenerative spondylolisthesis grade I or II with an indication for spinal fusion of one vertebral segment (L1-S1). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) PL (Completed) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003184-62 | Sponsor Protocol Number: J1369 | Start Date*: 2014-04-23 | |||||||||||
| Sponsor Name:Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins | |||||||||||||
| Full Title: A phase I study of SGI-110 combined with irinotecan followed by a randomized phase II study of SGI-110 combined with irinotecan versus regorafenib in previously treated metastatic colorectal cancer... | |||||||||||||
| Medical condition: Previously treated metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002799-28 | Sponsor Protocol Number: TG4001.12 | Start Date*: 2020-03-19 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Transgene | ||||||||||||||||||||||||||||||||||||||
| Full Title: A phase Ib/II trial evaluating the combination of TG4001 and avelumab in patients with HPV-16 positive recurrent or metastatic malignancies including oropharyngeal squamous cell carcinoma of the he... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: HPV-16 positive recurrent or metastatic malignancies including oropharyngeal squamous cell carcinoma of head and neck, cervical cancer, vulvar cancer, vaginal cancer, penile cancer, anal cancer | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2014-003774-16 | Sponsor Protocol Number: EIFFEL | Start Date*: 2016-06-07 |
| Sponsor Name:A.R.T.I.C. (Association pour la Recherche de Thérapeutiques Innovantes en Cancérologie ) | ||
| Full Title: Phase I/II dose-finding, safety and efficacy study of radium-223 dichloride (XOFIGO®) in renal cell carcinoma patients with bone metastases | ||
| Medical condition: Renal cell carcinoma patients with bone metastases, with or without visceral metastases. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001862-41 | Sponsor Protocol Number: CBYL719A2201 | Start Date*: 2013-11-26 |
| Sponsor Name:Novartis Farmacéutica , S.A. | ||
| Full Title: A phase II randomized, double-blind placebo controlled, study of letrozole with or without BYL719 or buparlisib, for the neoadjuvant treatment of postmenopausal women with hormone receptor-positive... | ||
| Medical condition: neoadjuvant hormone-receptor positive HER2-negative breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: ES (Completed) IT (Completed) AT (Completed) BE (Completed) DE (Completed) NL (Completed) CZ (Completed) BG (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002732-24 | Sponsor Protocol Number: FP2CLI001 | Start Date*: 2018-11-29 | |||||||||||
| Sponsor Name:Faron Pharmaceuticals Ltd | |||||||||||||
| Full Title: A Phase I/II Open–Label, Three-Part, Dose-Finding and Separate Cohort Expansion Trial to Assess the Safety, Tolerability and Preliminary Efficacy of Repeated Doses of CLEVER-1 Antibody FP-1305, in ... | |||||||||||||
| Medical condition: Selected solid tumours; - cutaneous melanoma - pancreatic ductal adenocarcinoma - ovarian cancer - colorectal adenocarcinoma - hepatocellular carcinoma - gallbladder cancer and cholangiocarcinoma... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) GB (GB - no longer in EU/EEA) NL (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005448-21 | Sponsor Protocol Number: H8O-EW-GWBE | Start Date*: 2006-06-30 |
| Sponsor Name:Eli Lilly and Company Ltd. | ||
| Full Title: Long-Term Treatment with Exenatide versus Glimepiride in Patients with Type 2 Diabetes Pretreated with Metformin | ||
| Medical condition: Type 2 diabetes mellitus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) ES (Completed) DE (Completed) HU (Completed) IT (Completed) IE (Completed) AT (Completed) CZ (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004198-28 | Sponsor Protocol Number: BAY1000394/14615 | Start Date*: 2014-06-18 |
| Sponsor Name:Bayer AG | ||
| Full Title: A randomized, double blind, placebo-controlled, multicenter phase II study to evaluate efficacy and safety of roniciclib in subjects with extensive-stage disease small cell lung cancer (SCLC) who a... | ||
| Medical condition: extensive-stage disease small cell lung cancer (ED SCLC) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) BE (Completed) HU (Completed) IT (Completed) PL (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002013-21 | Sponsor Protocol Number: THR-1442-C-480 | Start Date*: 2016-09-01 | |||||||||||
| Sponsor Name:Theracos Sub, LLC | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Active-controlled Study to Evaluate the Effects of Bexagliflozin versus Glimepiride in Subjects with Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Contr... | |||||||||||||
| Medical condition: Diabetes Mellitus Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004959-23 | Sponsor Protocol Number: NPJ005-DM2-0521 | Start Date*: 2018-07-05 | |||||||||||
| Sponsor Name:neopharma Japan Co., Ltd | |||||||||||||
| Full Title: A 24-week, Phase IIa, Double blind, Randomized, Parallel Group, Placebo controlled, Exploratory Study to Evaluate the Efficacy and Safety of 5 Aminolevulinic Acid Co-administered with Sodium Ferrou... | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus in Patients who have not Achieved Adequate Glycemic Control with Maximum Tolerated Dose of Metformin Daily or Sulfonylurea | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002722-13 | Sponsor Protocol Number: BV-ICE | Start Date*: 2016-01-11 | |||||||||||
| Sponsor Name:LYSARC | |||||||||||||
| Full Title: Phase I/II feasibility study of Brentuximab Vedotin in refractory / relapsed Hodgkin lymphoma patients who are treated by chemotherapy (ICE) in second line and eligible for autologous transplantation | |||||||||||||
| Medical condition: Hodgkin Lymphoma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004179-33 | Sponsor Protocol Number: I8F-MC-GPGB | Start Date*: 2017-06-15 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Phase 2 Study of Once-Weekly LY3298176 Compared with Placebo and Dulaglutide in Patients with Type 2 Diabetes Mellitus | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002793-47 | Sponsor Protocol Number: MKIA-088-001 | Start Date*: 2019-01-16 | ||||||||||||||||
| Sponsor Name:NERVIANO MEDICAL SCIENCES SRL | ||||||||||||||||||
| Full Title: A Phase I/II Study of NMS-03592088, a FLT3, KIT and CSF1R Inhibitor, in Patients with Relapsed or Refractory AML or CMML | ||||||||||||||||||
| Medical condition: Acute myeloidleukemia (AML) or chronic myelomonocytic leukemia (CMML) relapsed or refractory. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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