- Trials with a EudraCT protocol (11,266)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11,266 result(s) found for: Test Two.
Displaying page 462 of 564.
| EudraCT Number: 2012-001767-71 | Sponsor Protocol Number: RX-3341-302 | Start Date*: 2013-06-20 | |||||||||||
| Sponsor Name:Melinta Therapeutics, Inc | |||||||||||||
| Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE BLIND, ACTIVE CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF DELAFLOXACIN COMPARED WITH VANCOMYCIN + AZTREONAM IN PATIENTS WITH ACUTE BACTERIAL S... | |||||||||||||
| Medical condition: ACUTE BACTERIAL SKIN AND SKIN STRUCTURE INFECTIONS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) LV (Completed) ES (Completed) BG (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002181-23 | Sponsor Protocol Number: CL3-20098-076 | Start Date*: 2015-12-14 | |||||||||||
| Sponsor Name:Institut de Recherche International Servier | |||||||||||||
| Full Title: Efficacy and safety of 2 doses of agomelatine (10mg, 25mg) given orally in children (from 7 to less than 12 years) and adolescents (from 12 to less than 18 years) with moderate to severe Major Depr... | |||||||||||||
| Medical condition: Major Depressive Disorder | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) HU (Completed) DE (Ongoing) BG (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000905-38 | Sponsor Protocol Number: PCYC-1137-CA | Start Date*: 2015-12-17 | |||||||||||
| Sponsor Name:Pharmacyclics LLC | |||||||||||||
| Full Title: A randomized, multicenter, double-blind, placebo-controlled, Phase 3 study of the Bruton’s Tyrosine Kinase inhibitor ibrutinib in combination with nab-paclitaxel and gemcitabine versus placebo in c... | |||||||||||||
| Medical condition: metastatic pancreatic adenocarcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) BE (Completed) FR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001659-37 | Sponsor Protocol Number: 26061 | Start Date*: 2007-06-25 | |||||||||||
| Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
| Full Title: Phase II Study of ZK 219477 in patients with recurrent glioblastoma | |||||||||||||
| Medical condition: Phase II study of ZK 219477 in patients with recurrent glioblastoma. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) NL (Completed) IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005327-63 | Sponsor Protocol Number: NN7088-4033 | Start Date*: 2016-12-08 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A multi-centre, comparative, double blind, randomised cross-over trial investigating single dose pharmacokinetics and safety of turoctocog alfa pegol from the pivotal process and turoctocog alfa pe... | |||||||||||||
| Medical condition: Haemophilia A | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: NL (Completed) DK (Completed) DE (Completed) ES (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003657-26 | Sponsor Protocol Number: ARD10248 | Start Date*: 2012-01-16 | |||||||||||
| Sponsor Name:sanofi aventis recherche et développement | |||||||||||||
| Full Title: An open label non-randomized phase 2 study evaluating SAR3419, an anti-CD19 antibody – maytansine conjugate, administered as single agent by intravenous infusion to patients with relapsed or refrac... | |||||||||||||
| Medical condition: Diffuse large B-cell lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) BE (Completed) ES (Completed) IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002579-33 | Sponsor Protocol Number: EE-301 | Start Date*: 2020-03-26 | |||||||||||
| Sponsor Name:Phathom Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Two-Phase, Multicenter Study to Evaluate the Efficacy and Safety of Vonoprazan 20 mg Compared to Lansoprazole 30 mg for Healing in Patients with Erosive Esophag... | |||||||||||||
| Medical condition: Erosive Esophagitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) HU (Completed) PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002810-37 | Sponsor Protocol Number: RI-01-007 | Start Date*: 2020-03-09 | |||||||||||
| Sponsor Name:Dr. Reddy’s Laboratories S.A. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Parallel Group, Multicenter Study to Assess the Immunogenicity and Safety of Transitioning Subjects With Rheumatoid Arthritis to Biosimilar Rituximab (DRL_RI) or Continu... | |||||||||||||
| Medical condition: Rheumatoid Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DE (Completed) LT (Completed) PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002239-11 | Sponsor Protocol Number: MYK-491-003 | Start Date*: 2019-04-18 |
| Sponsor Name:MyoKardia Inc. | ||
| Full Title: Randomized, Double-blind, Placebo-controlled, Two-Part, Adaptive Design Study of Safety, Tolerability, Preliminary Pharmacokinetics, and Pharmacodynamics of Single and Multiple Ascending Oral Doses... | ||
| Medical condition: Heart Failure with Reduced Ejection Fraction | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) GB (Completed) SE (Completed) NL (Ongoing) PL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001776-15 | Sponsor Protocol Number: MS202202-0002 | Start Date*: 2020-11-16 | |||||||||||
| Sponsor Name:Merck Healthcare KGaA | |||||||||||||
| Full Title: A Phase II single-arm study to investigate tepotinib combined with cetuximab in RAS/BRAF wild-type left-sided metastatic colorectal cancer (mCRC) patients having acquired resistance to anti-EGFR... | |||||||||||||
| Medical condition: left-sided metastatic colorectal cancer (mCRC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Prematurely Ended) CZ (Prematurely Ended) BE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002630-32 | Sponsor Protocol Number: NN6435-4697 | Start Date*: 2021-07-27 | ||||||||||||||||
| Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
| Full Title: Dose response and safety of an oral PCSK9i, NNC0385-0434, in patients with established atherosclerotic cardiovascular disease (ASCVD) or ASCVD risk on maximally tolerated statin dose and other lipi... | ||||||||||||||||||
| Medical condition: Established atherosclerotic cardiovascular disease (ASCVD) or ASCVD risk Elevated cholesterol | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) GR (Completed) NL (Completed) BE (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-003609-24 | Sponsor Protocol Number: MB09-C-01-19 | Start Date*: 2021-12-30 | |||||||||||
| Sponsor Name:mAbxience Research S.L. | |||||||||||||
| Full Title: A randomised, double-blind, parallel, multicentre, multinational study to compare the efficacy, pharmacokinetics, pharmacodynamics, safety and immunogenicity of MB09 (proposed denosumab biosimilar)... | |||||||||||||
| Medical condition: Postmenopausal women diagnosed with osteoporosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: EE (Completed) BG (Completed) PL (Completed) LV (Completed) HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000662-38 | Sponsor Protocol Number: D419NC00001 | Start Date*: 2017-01-18 |
| Sponsor Name:MedImmune, LLC, a wholly owned subsidiary of AstraZeneca PLC | ||
| Full Title: A Phase 1 Study of Durvalumab and IPH2201 in Adult Subjects with Select Advanced Solid Tumors | ||
| Medical condition: Advanced solid tumor | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) ES (Ongoing) FR (Completed) BE (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003228-22 | Sponsor Protocol Number: AC16092 | Start Date*: 2016-12-14 | |||||||||||
| Sponsor Name:University of Edinburgh [...] | |||||||||||||
| Full Title: Treatment of Osteogenesis Imperfecta with Parathyroid hormone and Zoledronic acid | |||||||||||||
| Medical condition: Osteogenesis imperfecta | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) IE (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-004811-26 | Sponsor Protocol Number: ALK22/ENZ215-DEN2 | Start Date*: 2022-02-21 | |||||||||||
| Sponsor Name:Alkem Laboratories Limited | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Parallel-group, Active-controlled Study to Compare the Efficacy, Safety, Pharmacodynamics, Pharmacokinetics and Immunogenicity of Enzene Denosumab (ENZ215) and ... | |||||||||||||
| Medical condition: Postmenopausal osteoporosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: LT (Prohibited by CA) DK (Completed) ES (Ongoing) BG (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000722-38 | Sponsor Protocol Number: 1203-GITCG | Start Date*: 2015-05-25 | |||||||||||
| Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
| Full Title: INtegratioN of trastuzumab, with or without pertuzumab, into periOperatiVe chemotherApy of HER-2 posiTIve stOmach caNcer: the INNOVATION-TRIAL | |||||||||||||
| Medical condition: HER-2 positive, resectable gastric cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Completed) DE (Completed) BE (Completed) NO (Completed) PT (Completed) GB (GB - no longer in EU/EEA) ES (Completed) NL (Completed) FR (Completed) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004339-35 | Sponsor Protocol Number: AR-301-002 | Start Date*: 2019-01-16 | |||||||||||
| Sponsor Name:Aridis Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Randomized double-blind placebo-controlled multicenter Phase 3 study of efficacy and safety of AR-301 as adjunct therapy to antibiotics in the treatment of Ventilator-Associated Pneumonia (VAP) c... | |||||||||||||
| Medical condition: Staphylococcus aureus pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Completed) FR (Completed) LV (Completed) BE (Completed) ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004076-34 | Sponsor Protocol Number: 7487-CL-0209 | Start Date*: 2014-02-27 | ||||||||||||||||||||||||||
| Sponsor Name:Astellas Pharma Global Development, Inc. | ||||||||||||||||||||||||||||
| Full Title: A phase II open-label rollover study for subjects that have participated in an Astellas sponsored linsitinib trial | ||||||||||||||||||||||||||||
| Medical condition: Solid tumors | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: CZ (Completed) PL (Completed) GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-005964-15 | Sponsor Protocol Number: IMCL CP12-0715 | Start Date*: 2010-01-08 | |||||||||||
| Sponsor Name:IMCLONE LLC | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blinded Study of IMC-1121B and Best Supportive Care (BSC) Versus Placebo and BSC in the Treatment of Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma Fol... | |||||||||||||
| Medical condition: Metastatic Gastric Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) ES (Completed) CZ (Completed) MT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013094-17 | Sponsor Protocol Number: HOVON103AMLLEN | Start Date*: 2010-04-13 | |||||||||||||||||||||
| Sponsor Name:HOVON Foundation | |||||||||||||||||||||||
| Full Title: A randomized phase II multicenter study with a safety run-in to assess the tolerability and efficacy of the addition of oral lenalidomide to standard induction therapy in AML and RAEB ≥ 66 years an... | |||||||||||||||||||||||
| Medical condition: patients ≥ 66 years.with a confirmed diagnosis of o AML (not APL) (see appendix A) or o refractory anemia with excess of blasts (RAEB) with an IPSS score ≥ 1.5 OR Patients of any age ≥ 1... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Ongoing) BE (Completed) NO (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
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