- Trials with a EudraCT protocol (44,381)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,381 result(s) found.
Displaying page 1,584 of 2,220.
| EudraCT Number: 2019-001793-28 | Sponsor Protocol Number: 371b | Start Date*: 2019-11-05 |
| Sponsor Name:Reade | ||
| Full Title: Adalimumab dose reduction aiming low serum concentration with control of disease activity (ADDORA-LOW) : a single blind, non-inferiority, randomised clinical trial | ||
| Medical condition: Rheumatoid arthritis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002431-18 | Sponsor Protocol Number: NN9536-4451 | Start Date*: 2019-09-25 | ||||||||||||||||
| Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
| Full Title: Effect and safety of semaglutide 2.4 mg once weekly on weight management in adolescents with overweight or obesity | ||||||||||||||||||
| Medical condition: Overweight Obesity | ||||||||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) AT (Completed) BE (Completed) IE (Completed) HR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-001268-20 | Sponsor Protocol Number: EP0073 | Start Date*: 2015-08-13 | |||||||||||
| Sponsor Name:UCB Biopharma SRL | |||||||||||||
| Full Title: AN OPEN-LABEL, MULTICENTER, EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY, TOLERABILITY, AND EFFICACY OF UCB0942 WHEN USED AS ADJUNCTIVE THERAPY FOR PARTIAL-ONSET SEIZURES IN ADULT SUBJECTS WITH... | |||||||||||||
| Medical condition: highly drug-resistant focal epilepsy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) BE (Completed) BG (Completed) HU (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002023-41 | Sponsor Protocol Number: CRC1 | Start Date*: 2013-10-28 | |||||||||||
| Sponsor Name:VU University Medical Center | |||||||||||||
| Full Title: Image guided treatment optimalization with cetuximab for patients with metastatic colorectal cancer: IMPACT - CRC | |||||||||||||
| Medical condition: metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004557-14 | Sponsor Protocol Number: NA | Start Date*: 2015-02-09 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: Prospective randomised marker-based trial to assess the clinical utility and safety of biomarker-guided immunosuppression withdrawal in liver transplantation | |||||||||||||
| Medical condition: Immunosuppression withdrawal in liver transplantation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001543-30 | Sponsor Protocol Number: R3500-AD-1798 | Start Date*: 2019-06-11 | |||||||||||
| Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PHASE 2A STUDY TO ASSESS THE EFFICACY AND SAFETY OF REGN3500 MONOTHERAPY AND COMBINATION OF REGN3500 PLUS DUPILUMAB IN ADULT PATIENTS WITH MODERATE-T... | |||||||||||||
| Medical condition: Moderate to Severe Atopic Dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) BE (Completed) ES (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002821-45 | Sponsor Protocol Number: AC-055H302 | Start Date*: 2019-03-05 | ||||||||||||||||
| Sponsor Name:Actelion Pharmaceuticals Ltd | ||||||||||||||||||
| Full Title: Prospective, multi-center, single-arm, open-label long-term study assessing the safety, tolerability, and effectiveness of macitentan in Fontan-palliated adult and adolescent subjects | ||||||||||||||||||
| Medical condition: Congenital Heart Failure | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) DE (Completed) GB (GB - no longer in EU/EEA) DK (Completed) PL (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-000126-26 | Sponsor Protocol Number: V419-013 | Start Date*: 2020-07-21 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | |||||||||||||
| Full Title: A Hepatitis B Vaccine Challenge Study to Demonstrate the Durability of Protection Against Hepatitis B Virus Infection in Healthy Children Vaccinated Approximately 9 Years Previously With a 2- or 3-... | |||||||||||||
| Medical condition: Long-term protection against HBV infection | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002201-25 | Sponsor Protocol Number: CHDR2007 | Start Date*: 2020-12-14 |
| Sponsor Name:Centre for Human Drug Research | ||
| Full Title: A two-part (observational and intervention) study to explore disease characteristics of vulvar (pre)malignancies compared to healthy volunteers | ||
| Medical condition: lichen sclerosus, vulvar (pre)malignancies | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004882-15 | Sponsor Protocol Number: STOP-NUC | Start Date*: 2014-10-30 | |||||||||||
| Sponsor Name:Universität Leipzig | |||||||||||||
| Full Title: A multicentre randomized controlled trial evaluating the rate of sustained remission and the safety when stopping nucleos(t)ide analogue treatment in non-cirrhotic HBeAg-negative chronic Hepatitis ... | |||||||||||||
| Medical condition: HBeAg negative chronic Hepatitis B virus (HBV) infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004675-13 | Sponsor Protocol Number: WIL-31 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Octapharma AG | |||||||||||||
| Full Title: CLINICAL STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF WILATE DURING PROPHYLAXIS IN PREVIOUSLY TREATED PATIENTS WITH VON WILLEBRAND DISEASE (VWD) | |||||||||||||
| Medical condition: Von Willebrand disease, type 3, type 2 (except 2N), or severe type 1 | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) HU (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000400-26 | Sponsor Protocol Number: 201842 | Start Date*: 2015-12-15 | |||||||||||
| Sponsor Name:GlaxoSmithKline R&D Ltd | |||||||||||||
| Full Title: A randomized, double blind (sponsor open), comparative, multicenter study to evaluate the safety and efficacy of subcutaneous belimumab (GSK1550188) and intravenous rituximab coadministration in su... | |||||||||||||
| Medical condition: Primary Sjogrens disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) NO (Completed) DE (Completed) ES (Completed) NL (Completed) GB (Completed) FR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003650-88 | Sponsor Protocol Number: BAY94-9343/15743 | Start Date*: 2015-11-25 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: A randomized, open-label, active-controlled, Phase II study of intravenous anetumab ravtansine (BAY 94-9343) or vinorelbine in patients with advanced or metastatic malignant pleural mesothelioma ov... | |||||||||||||
| Medical condition: Patients with advanced or metastatic malignant pleural mesothelioma overexpressing mesothelin | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) DE (Completed) BE (Completed) GB (Completed) ES (Completed) NL (Completed) PL (Completed) FR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002668-28 | Sponsor Protocol Number: HP-301 | Start Date*: 2020-04-21 | |||||||||||
| Sponsor Name:Phathom Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 3 Randomized Multicenter Study to Evaluate the Efficacy and Safety of Open-Label Dual Therapy with Oral Vonoprazan 20 mg or Double-Blind Triple Therapy with Oral Vonoprazan 20 mg Compared t... | |||||||||||||
| Medical condition: Helicobacter pylori infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002009-25 | Sponsor Protocol Number: SARSCov2EFTI1.0 | Start Date*: 2020-10-01 |
| Sponsor Name:Fakultní nemocnice Plzeň | ||
| Full Title: The efficacy and safety of Eftilagimod Alpha Treatment by immune modulation in COVID-19 disease (EAT COVID trial) | ||
| Medical condition: COVID-19 disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004901-28 | Sponsor Protocol Number: EDP1815-201 | Start Date*: 2020-03-31 | |||||||||||
| Sponsor Name:Evelo Biosciences Inc. | |||||||||||||
| Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Cohort, Dose-Ranging Study Investigating the Effect of EDP1815 in the Treatment of Mild to Moderate Plaque Psoriasis | |||||||||||||
| Medical condition: Mild to Moderate Plaque Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001852-32 | Sponsor Protocol Number: 3475-164 | Start Date*: 2015-12-11 |
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
| Full Title: A Phase II Study of Pembrolizumab (MK-3475) as Monotherapy in Subjects with Previously Treated Locally Advanced Unresectable or Metastatic (Stage IV) Mismatched Repair Deficient or Microsatellite I... | ||
| Medical condition: Colorectal Carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) BE (Completed) ES (Completed) FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-002061-12 | Sponsor Protocol Number: SBG2004-1/ABCSG25/GBG53 | Start Date*: 2007-08-17 | |||||||||||
| Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | |||||||||||||
| Full Title: PANTHER (The SBG 2004-1/ABCSG 25/GBG53 Protocol) - a randomised phase III study: Comparing two weekly and tailored epirubicin + cyclophosphamide followed by two weekly tailored docetaxel (dtEC->dtT... | |||||||||||||
| Medical condition: lymph node positive breast cancer patients | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: AT (Completed) FI (Prematurely Ended) DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002856-34 | Sponsor Protocol Number: LTx18-01 | Start Date*: 2019-03-01 | |||||||||||
| Sponsor Name:Foundation for Liver research | |||||||||||||
| Full Title: Modifying tacrolimus related toxicity after liver transplantation. A randomized controlled trial comparing Envarsus® and Advagraf® in de novo liver transplant recipients. | |||||||||||||
| Medical condition: liver transplantation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004364-21 | Sponsor Protocol Number: FYB202-03-01 | Start Date*: 2020-05-12 | |||||||||||
| Sponsor Name:bioeq GmbH | |||||||||||||
| Full Title: A Randomised, Double-blind, Parallel-group, Phase 3 Study to Compare the Efficacy, Safety, and Immunogenicity of the Proposed Biosimilar Ustekinumab FYB202 to Stelara in Patients with Moderate-to-S... | |||||||||||||
| Medical condition: Moderate-to-Severe Plaque Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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