- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,380 result(s) found.
Displaying page 910 of 2,219.
| EudraCT Number: 2013-001885-41 | Sponsor Protocol Number: DLX105-003-002-001 | Start Date*: 2013-07-11 | |||||||||||
| Sponsor Name:Delenex Therapeutics AG | |||||||||||||
| Full Title: A multi-center, double-blinded, randomized, placebo-controlled, phase II study to evaluate the safety, tolerability and efficacy of a topical application of DLX105 onto lesional skin in patients wi... | |||||||||||||
| Medical condition: mild-to-moderate plaque-type psoriasis vulgaris 6 (PASI ≤15) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003120-21 | Sponsor Protocol Number: GFM-Acadesine | Start Date*: 2013-04-15 | |||||||||||
| Sponsor Name:Groupe Francophone des Myélodysplasies (GFM) | |||||||||||||
| Full Title: A phaseI-II trial of acadesine in ipss high and int 2 myelodysplastic syndromes, acute myeloid leukemia with 20-30% marrow blasts and chronic myelomonocytic leukemia type 2 not responding to azacit... | |||||||||||||
| Medical condition: MYELODYSPLASTIC SYNDROMES | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005330-10 | Sponsor Protocol Number: 987654321 | Start Date*: 2013-03-14 |
| Sponsor Name:Erasmus University Medical Centre | ||
| Full Title: Maternal pharmacokinetics and pharmacodynamics of nicardipine (iv) during treatment of severe hypertension in pregnancy. | ||
| Medical condition: Pregnant patients with preeclampsia (hypertension and protein/creatinine ratio ≥ 30mg/mmol or ≥ 300mg protein/24hours) complicated with severe hypertension (systolic bloodpressure ≥ 160mmHg and/or ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001326-25 | Sponsor Protocol Number: ACA-SPAI-11-24 | Start Date*: 2013-07-25 | |||||||||||
| Sponsor Name:Fundación SENEFRO | |||||||||||||
| Full Title: Efficacy and safety of paricalcitol in the reduction of secondary hyperparathyroidism after renal transplantation. | |||||||||||||
| Medical condition: Secondary hyperparathyroidism after renal transplantation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002145-35 | Sponsor Protocol Number: ABC-2011-NSCLC-03 | Start Date*: 2013-06-14 | |||||||||||
| Sponsor Name:Aktion Bronchialkarzinom (ABC) e.V. | |||||||||||||
| Full Title: SELECT-A: TS stratified Chemotherapy and VEGF Inhibition in Non-Squamous Non-Small Cell Lung Cancer - Stage IV | |||||||||||||
| Medical condition: Non-squamous advanced Non-Small-Cell Lung-Cancer (Stage IV) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-001538-41 | Sponsor Protocol Number: | Start Date*: 2011-06-29 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: The impact of the combination of the GLP-1 analogue liraglutide (Victoza) and laparoscopic adjustable gastric banding (LAGB) on diabetes control | |||||||||||||
| Medical condition: This trial will investigate the effects of the study treatment arms (gastric band + placebo; gastric band + liraglutide) on diabetes resolution in obese patients. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000833-11 | Sponsor Protocol Number: CBKM120D2205 | Start Date*: 2013-07-11 | |||||||||||||||||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||||||||||||
| Full Title: A Phase Ib/II study of docetaxel with or without buparlisib as second line therapy for patients with advanced or metastatic squamous non-small cell lung cancer | |||||||||||||||||||||||||||||||||
| Medical condition: advanced/metastatic squamous non small cell lung cancer | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: SE (Prematurely Ended) IT (Completed) DE (Completed) ES (Completed) GB (Completed) BE (Completed) HU (Prematurely Ended) NO (Prematurely Ended) FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-006180-21 | Sponsor Protocol Number: CA180-400 | Start Date*: 2013-02-19 | |||||||||||
| Sponsor Name:BRISTOL-MYERS SQUIBB INTERNATIONAL CORPORATION | |||||||||||||
| Full Title: A PHASE IV, OPEN-LABEL, MULTICENTER STUDY OF DASATINIB IN CHRONIC-PHASE CHRONIC MYELOID LEUKEMIA (CP-CML) PATIENTS WITH CHRONIC LOW-GRADE NONHEMATOLOGIC TOXICITY TO IMATINIB | |||||||||||||
| Medical condition: CP-CML patients with non hematologic low toxicity grade to imatinib | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004297-26 | Sponsor Protocol Number: 1632/12 | Start Date*: 2012-12-23 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Phase III clinical study of PET-TC with [18f]Fluoroethyilcholine ([18f]Fech) in prostate cancer: assessment of the additional role with respec to conventional imaging techniques | |||||||||||||
| Medical condition: prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003032-31 | Sponsor Protocol Number: P-110880-01 | Start Date*: 2012-02-22 | |||||||||||
| Sponsor Name:Ferrer Internacional, S.A. | |||||||||||||
| Full Title: A phase III 3 arms, multicenter, randomised, investigator-blind study to assess the efficacy and safety of ozenoxacin 1% cream applied twice daily for 5 days versus placebo in the treatment of pati... | |||||||||||||
| Medical condition: Impetigo | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004482-32 | Sponsor Protocol Number: RAS-ALS | Start Date*: 2013-04-10 | |||||||||||
| Sponsor Name:Universitätsklinikum Ulm | |||||||||||||
| Full Title: Efficacy, Safety and Tolerability Study of 1 mg Rasagiline in Patients with Amyotrophic Lateral Sclerosis (ALS) Receiving Standard Therapy (Riluzole) | |||||||||||||
| Medical condition: Amyotrophic Lateral Sclerosis (ALS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003806-28 | Sponsor Protocol Number: 31-12-297 | Start Date*: 2013-03-25 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, | |||||||||||||
| Full Title: A 26-week, Multicenter, Open-label, Extension Study of Aripiprazole Intramuscular Depot (OPC-14597, Lu AF41155) in Patients with Schizophrenia | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001545-42 | Sponsor Protocol Number: B9E-IT-S376 | Start Date*: 2005-07-13 | |||||||||||
| Sponsor Name:ELI LILLY | |||||||||||||
| Full Title: A Randomized Phase III Trial of Gemcitabine and Docetaxel versus Gemcitabine and Paclitaxel in Patients with Metastatic Breast Cancer: a comparison of different schedules | |||||||||||||
| Medical condition: Metatstatic breast cancer | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-006294-26 | Sponsor Protocol Number: 021101 | Start Date*: 2013-04-07 | ||||||||||||||||
| Sponsor Name:Baxter Innovations GmbH | ||||||||||||||||||
| Full Title: A Phase 3, Prospective, Open-label, Randomized Study to Evaluate Safety and Efficacy of Recombinant Activated FVII BI (rFVIIa BI) in the Treatment of Acute Bleeding Episodes per an On-demand Regime... | ||||||||||||||||||
| Medical condition: Hemophilia A or B with FVIII or FIX inhibitors | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male | |||||||||||||||||
| Trial protocol: ES (Completed) BE (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2006-003843-22 | Sponsor Protocol Number: CURE | Start Date*: 2006-10-24 | |||||||||||
| Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
| Full Title: prospeCtive study on intensive early rheumatoid arthritis treatment with adalimUmab: induction of REmission and maintenance - 'CURE' A Phase IV multicenter, randomized, double-blind study | |||||||||||||
| Medical condition: rheumatoid arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004618-40 | Sponsor Protocol Number: 20110100 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Amgen Inc. | |||||||||||||
| Full Title: An Open-label, Single-arm Study to Assess the Safety and Tolerability of Cinacalcet HCl in Addition to Standard of Care in Pediatric Subjects Age 28 Days to < 6 Years with Chronic Kidney Disease an... | |||||||||||||
| Medical condition: Secondary hyperparathyroidism in pediatric subjects with chronic kidney disease receiving hemodialysis or peritoneal dialysis | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) NL (Temporarily Halted) PL (Completed) HU (Completed) CZ (Completed) IT (Completed) SK (Completed) BE (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000474-42 | Sponsor Protocol Number: CL2-90652-002 | Start Date*: 2006-12-06 | |||||||||||
| Sponsor Name:INSTITUT DE RECHERCHES INTERNATIONALES SERVIER | |||||||||||||
| Full Title: Safety and effects on blood pressure of a daily dose of 0.025 to 0.135 milligram per kilogram of S 90652, a paediatric formulation of perindopril, in hypertensive children having received S 90652 -... | |||||||||||||
| Medical condition: Arterial Hypertension | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000679-18 | Sponsor Protocol Number: CV181-169 | Start Date*: 2012-11-13 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Active-Controlled, Parallel Group, Phase 3 Trial to Evaluate the Safety and Efficacy of Add-On Therapy with Saxagliptin and Dapagliflozin added to Metformin... | |||||||||||||
| Medical condition: Type 2 Diabetes who have Inadequate Glycemic Control on Metformin Alone | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005348-92 | Sponsor Protocol Number: PROGASS | Start Date*: 2013-02-19 | |||||||||||
| Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO DI MILANO | |||||||||||||
| Full Title: PROGASS PRucalopride On the GAstreonteric transit in Systemic Sclerosis | |||||||||||||
| Medical condition: Sysemic sclerosis with gastroenteric involvement (constipation) | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005843-28 | Sponsor Protocol Number: BERNAQ | Start Date*: 2013-04-30 | ||||||||||||||||
| Sponsor Name:Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla | ||||||||||||||||||
| Full Title: RANDOMIZED OPEN-LABEL, MULTICENTRIC, PHASE II CLINICAL TRIAL TO EVALUATE THE EFFICACY OF A NEOADJUVANT CHEMOTHERAPY SCHEME CUSTOMIZED BY LEVELS OF BRCA1 AND ERCC1 IN WOMEN WITH PRIMARY HER2 NEGATIV... | ||||||||||||||||||
| Medical condition: Primary breast cancer, ER or PgR positive, or triple negative and HER-2 negative, larger than 2 cm in diameter. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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