- Trials with a EudraCT protocol (1,699)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (14)
1,699 result(s) found for: Chemistry.
Displaying page 74 of 85.
| EudraCT Number: 2013-001037-40 | Sponsor Protocol Number: IFX-1-P2.1 | Start Date*: 2014-02-11 | |||||||||||
| Sponsor Name:InflaRx GmbH | |||||||||||||
| Full Title: A phase II randomized, placebo-controlled, double-blind, dose controlled trial in patients suffering from early, newly developing abdominal or pulmonary derived septic organ dysfunction to evaluate... | |||||||||||||
| Medical condition: septic organ dysfunction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000756-41 | Sponsor Protocol Number: DEB-EPIV-201 | Start Date*: 2006-04-24 |
| Sponsor Name:Debiopharm SA | ||
| Full Title: Phase IIa Multicenter 1 Week Treatment, Randomised, Double-Blind, Placebo Controlled Study of Depelestat in Patients Suffering from Acute Respiratory Distress Syndrome | ||
| Medical condition: Acute Respiratory Distress Syndrome (ARDS) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) ES (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000346-30 | Sponsor Protocol Number: CINC424XDE04T | Start Date*: 2015-03-16 | ||||||||||||||||
| Sponsor Name:Universität Leipzig | ||||||||||||||||||
| Full Title: An open-label, multicenter study of INC424 monotherapy or in combination with azacitidine for patients with post-myeloproliferative disorders (MPD) – AML or with CMML | ||||||||||||||||||
| Medical condition: Chronic Myelomonocytic Leukemia and secondary Acute myeloid leukemia | ||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-003257-15 | Sponsor Protocol Number: A083-02 | Start Date*: 2018-04-12 | |||||||||||
| Sponsor Name:Acceleron Pharma Inc. | |||||||||||||
| Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study of ACE-083 in Patients with Facioscapulohumeral Muscular Dystrophy | |||||||||||||
| Medical condition: Facioscapulohumeral Muscular Dystrophy | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003402-46 | Sponsor Protocol Number: CAN04CLIN005 | Start Date*: 2021-09-23 | |||||||||||
| Sponsor Name:Cantargia AB | |||||||||||||
| Full Title: A randomized non-comparative open-label phase 1b/2 study of nadunolimab in combination with gemcitabine plus carboplatin in patients with advanced triple negative breast cancer. “TRIFOUR study”. | |||||||||||||
| Medical condition: Unresectable locally advanced or metastatic triple negative breast cancer. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-004214-14 | Sponsor Protocol Number: P311-201 | Start Date*: 2016-10-13 | ||||||||||||||||
| Sponsor Name:Upsher-Smith Laboratories, Inc. | ||||||||||||||||||
| Full Title: A Phase 1/2 Dose-escalation of USL311 as Single Agent and in Combination with Lomustine (CCNU) in Subjects with Advanced Solid Tumors, with Subsequent Single Agent and Combination Phase 2 Cohorts f... | ||||||||||||||||||
| Medical condition: Advanced Solid Tumors/Relapsed/Recurrent Glioblastoma Multiforme (GBM) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-000516-37 | Sponsor Protocol Number: TS-020DESE | Start Date*: 2021-03-04 | |||||||||||
| Sponsor Name:TurnSole Biologics Llc | |||||||||||||
| Full Title: A Phase I/II open-label study for Azacitidine, initiated with a lead-in dose escalation pharmacokinetic Phase I/b part in the 20–50 mg/m2 range to evaluate safety in Hospitalized COVID-19 Patients ... | |||||||||||||
| Medical condition: COVID-19 patients with confirmed sever viral infection of SARS-COV-2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-002766-21 | Sponsor Protocol Number: 1199.33 | Start Date*: 2012-05-02 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Hellas | |||||||||||||
| Full Title: An open-label extension trial of the long term safety of oral BIBF 1120 in patients with Idiopathic Pulmonary Fibrosis (IPF) | |||||||||||||
| Medical condition: Idiopathic Pulmonary Fibrosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) PT (Completed) BE (Completed) ES (Completed) DE (Completed) FI (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) IT (Completed) IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000373-80 | Sponsor Protocol Number: DERM-101 | Start Date*: 2018-05-24 | ||||||||||||||||
| Sponsor Name:Dermecular Therapeutics, Inc. | ||||||||||||||||||
| Full Title: A Phase 1/2, Randomized, Double-Blind, Placebo-Controlled, Parallel-Arm Study of the Safety and Efficacy of LX3305, a Sphingosine-1-Phosphate Lyase Inhibitor, for Treatment of Darier’s Disease or H... | ||||||||||||||||||
| Medical condition: Darier’s Disease or Hailey-Hailey Disease | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-002348-99 | Sponsor Protocol Number: AUTH88622 | Start Date*: 2014-09-22 | ||||||||||||||||
| Sponsor Name:Aristotle University Thessaloniki | ||||||||||||||||||
| Full Title: A randomised, double blind, placebo-controlled study of the effect of liraglutide on arterial blood pressure in hypertensive patients with type 2 diabetes mellitus | ||||||||||||||||||
| Medical condition: Hypertention, Type 2 Diabetes | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-003696-30 | Sponsor Protocol Number: 201928 | Start Date*: 2016-03-11 | ||||||||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||||||||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled study to evaluate the safety, efficacy and changes in induced sputum and blood biomarkers following daily repeat doses of inhaled GSK2269557 for 12 we... | ||||||||||||||||||
| Medical condition: COPD | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-003396-18 | Sponsor Protocol Number: TMC114FD2HTX1007 | Start Date*: 2020-12-23 | |||||||||||
| Sponsor Name:Janssen Sciences Ireland UC | |||||||||||||
| Full Title: A Single-Dose, Open-Label, Randomized, Replicate Crossover Pivotal Bioequivalence Study in Healthy Adult Participants to Assess the Bioequivalence of Darunavir 675 mg, Emtricitabine 200 mg, and Ten... | |||||||||||||
| Medical condition: Healthy Volunteers; Human immunodeficiency virus type 1 (HIV-1) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005212-14 | Sponsor Protocol Number: 200812 | Start Date*: 2016-04-20 | |||||||||||
| Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
| Full Title: A phase IIIB, 24-week randomised, double-blind study to compare 'closed' triple therapy (FF/UMEC/VI) with 'open' triple therapy (FF/VI + UMEC), in subjects with chronic obstructive pulmonary diseas... | |||||||||||||
| Medical condition: in subjects with chronic obstructive pulmonary disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) FR (Completed) RO (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-001810-16 | Sponsor Protocol Number: 62024 | Start Date*: 2004-11-25 | |||||||||||
| Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
| Full Title: Intermediate and high risk localized, completely resected, gastrointestinal stromal tumors (GIST) expressing KIT receptor: a controlled randomized trial on adjuvant Imatinib mesylate (Glivec) versu... | |||||||||||||
| Medical condition: Gastrointestinal stromal tumors (GIST) are mesenchymal neoplasms usually arising from the gastrointestinal wall. Pathologically,they present with spindle cells in most cases. Immunohistochemically... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) DK (Completed) GB (Completed) ES (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003796-17 | Sponsor Protocol Number: CST103/CST139-CLIN-010 | Start Date*: 2020-10-22 | ||||||||||||||||
| Sponsor Name:CuraSen Therapeutics, Inc. | ||||||||||||||||||
| Full Title: An Open-Label Brain Imaging and Cognition Study to Determine Changes in Cerebral Perfusion and Cognition After Oral Administration of CST-103 or CST-139 | ||||||||||||||||||
| Medical condition: Patients with Mild Cognitive Impairment or Parkinson’s Disease | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-004438-40 | Sponsor Protocol Number: GI1950 | Start Date*: 2020-04-06 | |||||||||||||||||||||
| Sponsor Name:Department of Oncology, Herlev & Gentofte Hospital | |||||||||||||||||||||||
| Full Title: Phase 2 study in pretreated patients with advanced pancreatic cancer to assess efficacy of ipilimumab, nivolumab and tocilizumab in combination with radiation. | |||||||||||||||||||||||
| Medical condition: Pretreated patients with advanced pancreatic cancer. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2021-000127-12 | Sponsor Protocol Number: TM006 | Start Date*: 2022-01-03 | |||||||||||
| Sponsor Name:Saniona A/S | |||||||||||||
| Full Title: A Phase 2b, Double-blind, Randomized, Placebo-controlled, Multi center, 16-week Dose finding, Safety and Efficacy Study with Open-label Extension Period of Tesomet in Adult and Adolescent Subjects ... | |||||||||||||
| Medical condition: Prader-Willi Syndrome | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001337-40 | Sponsor Protocol Number: BXCL501-105 | Start Date*: 2021-10-05 | |||||||||||||||||||||
| Sponsor Name:BioXcel Therapeutics, Inc. | |||||||||||||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO DETERMINE EFFICACY AND SAFETY OF BXCL501 IN AGITATION ASSOCIATED WITH PEDIATRIC SCHIZOPHRENIA AND BIPOLAR DISORDER | |||||||||||||||||||||||
| Medical condition: Subject that meets DSM-5 criteria for schizophrenia, schizoaffective, or schizophreniform disorder, or other specified/unspecified schizophrenia spectrum and/or other psychotic disorders OR Subjec... | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Restarted) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2020-005576-35 | Sponsor Protocol Number: CP-PRO-CoVLP-021 | Start Date*: 2021-05-06 | |||||||||||
| Sponsor Name:Medicago R&D Inc. | |||||||||||||
| Full Title: A Randomized, Observer-Blind, Placebo-Controlled, Phase 2/3 Study to Assess the Safety, Efficacy, and Immunogenicity of a Recombinant Coronavirus-Like Particle COVID-19 Vaccine in Adults 18 Years o... | |||||||||||||
| Medical condition: Covid-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000931-35 | Sponsor Protocol Number: D6470C00005 | Start Date*: 2020-10-05 | |||||||||||
| Sponsor Name:AstraZeneca AB, 151 85 Södertälje, Sweden | |||||||||||||
| Full Title: A Phase 2a Randomised, Double Blind, Multi-centre Study to Assess the Effect on Glucose Homeostasis of Two Dose Levels of AZD9567, Compared to Prednisolone, in Adults with Type 2 Diabetes | |||||||||||||
| Medical condition: Type 2 Diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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