- Trials with a EudraCT protocol (25,223)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
25,223 result(s) found.
Displaying page 967 of 1,262.
EudraCT Number: 2015-001316-34 | Sponsor Protocol Number: I5B-MC-JGDL | Start Date*: 2016-01-26 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 1b (Open-Label) / Phase 2 (Randomized, Double-Blinded) Study Evaluating Gemcitabine and Docetaxel With or Without Olaratumab in the Treatment of Advanced Soft Tissue Sarcoma | |||||||||||||
Medical condition: soft tissue sarcoma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) DE (Prematurely Ended) PL (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004374-15 | Sponsor Protocol Number: PUMA-NER-6201 | Start Date*: 2018-04-13 | |||||||||||
Sponsor Name:Puma Biotechnology, Inc. | |||||||||||||
Full Title: An Open Label Study to Characterize the Incidence and Severity of Diarrhea in Patients with Early Stage HER2+ Breast Cancer Treated with Neratinib and Intensive Loperamide Prophylaxis | |||||||||||||
Medical condition: Early Stage HER2+ Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003778-42 | Sponsor Protocol Number: CC-122-DLBCL-002 | Start Date*: 2017-07-31 |
Sponsor Name:Celgene Corporation | ||
Full Title: A Phase 1/2 Open-label, Multicenter Study of CC-122 in Combination With R-CHOP-21 for Previously Untreated Poor-Risk (IPI ≥ 3) Diffuse Large B-Cell Lymphoma | ||
Medical condition: Previously untreated, high-intermediate and high-risk (International Prognostic Index [IPI] ≥ 3) diffuse large B-cell lymphoma (DLBCL). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000889-29 | Sponsor Protocol Number: CLNP023X2202 | Start Date*: 2018-12-13 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: An open-label, non-randomized study on efficacy, pharmacokinetics, pharmacodynamics, safety and tolerability of LNP023 in two patient populations with C3 glomerulopathy | ||
Medical condition: C3 glomerulopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) DE (Completed) FR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001368-40 | Sponsor Protocol Number: M-41008-41 | Start Date*: 2017-09-13 | |||||||||||
Sponsor Name:Almirall S.A. | |||||||||||||
Full Title: Open clinical study to assess long-term efficacy and safety of dimethyl fumarate in adults with moderate to severe chronic plaque psoriasis in real practice (DIMESKIN 1 Trial) | |||||||||||||
Medical condition: Moderate-severe chronic plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003466-28 | Sponsor Protocol Number: DS8201-A-J203 | Start Date*: 2018-06-26 | |||||||||||
Sponsor Name:Daiichi Sankyo Inc. | |||||||||||||
Full Title: A PHASE 2, MULTICENTER, OPEN-LABEL STUDY OF DS-8201A IN SUBJECTS WITH HER2-EXPRESSING ADVANCED COLORECTAL CANCER [DESTINY-CRC01] | |||||||||||||
Medical condition: Human epidermal growth factor receptor 2 (HER2)- expressing advanced colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004486-27 | Sponsor Protocol Number: X31005 | Start Date*: 2018-02-12 |
Sponsor Name:Associació Per a la Recerca Oncològica(APRO) | ||
Full Title: Phase II Study of Paclitaxel and TAK-228 in metastatic urothelial carcinoma (UC) and the impact of PI3K-mTOR pathway genomic alterations | ||
Medical condition: Metastatic urothelial carcinoma (UC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004556-27 | Sponsor Protocol Number: D933IC00003 | Start Date*: 2018-04-29 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Randomized, Multi-Center, Double-Blind, Comparative Global Study to Determine the Efficacy and Safety of Durvalumab in Combination With Olaparib for First-Line Treatment in Cisplatin-In... | |||||||||||||
Medical condition: Unresectable Stage IV Urothelial Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020951-30 | Sponsor Protocol Number: SPD489-404 | Start Date*: 2011-03-03 | |||||||||||
Sponsor Name:Shire Pharmaceutical Development Ltd | |||||||||||||
Full Title: A Phase 4, Open-label, Multicentre, 2-Year Safety Study of Lisdexamfetamine Dimesylate in Children and Adolescents Aged 6-17 Years with Attention-Deficit/Hyperactivity Disorder (ADHD) | |||||||||||||
Medical condition: Attention Deficit/Hyperactivity Disorder (ADHD) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) BE (Completed) ES (Completed) SE (Completed) PL (Completed) DE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000596-42 | Sponsor Protocol Number: 109621 | Start Date*: 2007-10-30 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III open study to assess the safety, reactogenicity and immunogenicity following booster administration of GlaxoSmithKline (GSK) Biologicals´ 10-valent pneumococcal conjugate vaccine, co-ad... | ||
Medical condition: Booster vaccination against Streptococcus pneumoniae of healthy preterm born children between 16-18 months of age who were previously primed with three doses of GSK Biologicals’10-valent conjugate ... | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: GR (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002840-21 | Sponsor Protocol Number: HGT-GCB-039 | Start Date*: 2007-10-30 | |||||||||||
Sponsor Name:Shire Human Genetic Therapies Inc | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel-Group Study of Gene-Activated® Human Glucocerebrosidase (GA-GCB) Enzyme Replacement Therapy Compared with Imiglucerase in Patients with Type I Gauc... | |||||||||||||
Medical condition: Type I Gaucher disease Enfermedad de Gaucher tipo 1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001634-36 | Sponsor Protocol Number: SARCOVID | Start Date*: 2020-04-09 |
Sponsor Name:Rosario García de Vicuña | ||
Full Title: Randomized open pilot study to evaluate the efficacy of subcutaneous sarilumab in patients with moderate-severe COVID-19 infection. | ||
Medical condition: COVID-19 infection requiring hospitalization | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005350-19 | Sponsor Protocol Number: TTD-14-05 | Start Date*: 2015-06-26 | |||||||||||
Sponsor Name:Grupo de Tratamiento de los Tumores Digestivos (TTD) | |||||||||||||
Full Title: A phase I/II study of nab-paclitaxel (Abraxane®) and gemcitabine followed by modified FOLFOX (AG-mFOLFOX) in patients with previously untreated, metastatic pancreatic adenocarcinoma | |||||||||||||
Medical condition: Metastatic pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005394-45 | Sponsor Protocol Number: MM09-STD-011 | Start Date*: 2015-09-03 | |||||||||||
Sponsor Name:Inmunotek, S.L. | |||||||||||||
Full Title: Dermatophagoides pteronyssinus and Dermatophagoides farinae allergen extract. Determination of the allergenic potency in vivo histamine equivalent units (HEP) | |||||||||||||
Medical condition: Allergy to mites: Dermatophagoides pteronyssinus and Dermatophagoides farinae | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004524-38 | Sponsor Protocol Number: GECP16/04 | Start Date*: 2017-03-06 |
Sponsor Name:Spanish Lung Cancer Group (Grupo Español de Cáncer de Pulmón) | ||
Full Title: A phase II exploratory study of durvalumab (MEDI4736) in HIV-1 patients with advanced solid tumors | ||
Medical condition: advanced solid tumors in HIV-1 infected patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001702-28 | Sponsor Protocol Number: MedOPP199 | Start Date*: 2018-11-27 | |||||||||||
Sponsor Name:Medica Scientia Innovation Research (MEDSIR) | |||||||||||||
Full Title: Neoadjuvant Letrozole and Palbociclib in patients with Stage II-IIIb breast cancer, HR (+) / HER2 (-) phenotype and Intermediate (18-25) or High (>25) Recurrence-Score by Oncotype-DX; analysis of R... | |||||||||||||
Medical condition: Early HR(+)/HER2(-) Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006304-11 | Sponsor Protocol Number: TKT034 | Start Date*: 2007-07-03 | |||||||||||
Sponsor Name:Shire Human Genetic Therapies Inc | |||||||||||||
Full Title: A multicenter open-label study of Gene-Activated Human Glucocerebrosidase (GA-GCB) enzyme replacement therapy in patients with type 1 Gaucher disease previously treated wiht imiglucerase | |||||||||||||
Medical condition: Type I Gaucher Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000864-29 | Sponsor Protocol Number: BO17704 | Start Date*: 2004-12-01 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A randomized, double-blind multicenter phase III study of bevacizumab in combination with cisplatin and gemcitabine versus placebo, cisplatin and gemcitabine in patients with advanced or recurrent ... | |||||||||||||
Medical condition: Advanced or recurrent non-squamous non-small cell lung cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002813-20 | Sponsor Protocol Number: 331-201-00242 | Start Date*: 2020-03-16 | ||||||||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Flexible-dose, Double-blind Trial of Brexpiprazole Versus Placebo for the Treatment of Adults With Borderline Personality Disorder | ||||||||||||||||||
Medical condition: Borderline Personality Disorder | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002743-27 | Sponsor Protocol Number: TKT024EXT | Start Date*: 2004-12-23 | |||||||||||
Sponsor Name:Shire Human Genetic Therapies INC. | |||||||||||||
Full Title: An Open-Label Extension of Study TKT024 Evaluating Long-Term Safety and Clinical Outcomes in MPS II Patients Receiving Iduronate-2-Sulfatase Enzyme Replacement Therapy | |||||||||||||
Medical condition: Mucopolysaccharidosis Type II (MPS II or Hunter Syndrome) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) SE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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