- Trials with a EudraCT protocol (44,394)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,394 result(s) found.
Displaying page 2,171 of 2,220.
| EudraCT Number: 2020-000649-16 | Sponsor Protocol Number: PRV-015-002b | Start Date*: 2021-04-06 | |||||||||||
| Sponsor Name:Provention Bio, Inc. | |||||||||||||
| Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of PRV-015 in Adult Patients with Non-Responsive Celiac Disease as an Adjunct to a... | |||||||||||||
| Medical condition: Celiac Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-002441-18 | Sponsor Protocol Number: D6582C00001 | Start Date*: 2022-10-27 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase IIa Randomised, Double-Blind, Placebo Controlled, Parallel Arm, Multi-Centre Study to Evaluate the Efficacy and Safety of AZD4831, for 12-24 Weeks, in Moderate to Severe Chronic Obstructive... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) ES (Ongoing) NL (Completed) IT (Completed) BG (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001923-30 | Sponsor Protocol Number: TN-20 | Start Date*: 2016-09-26 | |||||||||||
| Sponsor Name:TRIALNET COORDINATING CENTER AT THE UNIVERSITY OF SOUTH FLORIDA | |||||||||||||
| Full Title: Exploring Immune Effects of Oral Insulin in Relatives at Risk for Type 1 Diabetes Mellitus | |||||||||||||
| Medical condition: Type 1 Diabetes | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003851-12 | Sponsor Protocol Number: 20968 | Start Date*: 2020-06-25 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: Randomized, Double-Masked, Active-Controlled, Phase 3 Study of the Efficacy and Safety of High Dose Aflibercept in Patients With Neovascular Age-Related Macular Degeneration | |||||||||||||
| Medical condition: Neovascular Age-Related Macular Degeneration | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) LT (Completed) LV (Completed) PT (Completed) EE (Completed) AT (Completed) FR (Completed) SK (Completed) BG (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002644-23 | Sponsor Protocol Number: MB_PDT_1 | Start Date*: 2020-07-23 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Dept. of Dermatology, Zealand University Hospital, Roskilde | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Photodynamic therapy of antifungal resistant dermatophytes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Competent patients over 18 years old with mycological verified antifungal resistant dermatophytosis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-006788-11 | Sponsor Protocol Number: NBI-827104-CSWS2025 | Start Date*: 2022-03-25 | |||||||||||
| Sponsor Name:Neurocrine Biosciences, Inc. | |||||||||||||
| Full Title: Long-Term, Open-Label Extension Study to Evaluate the Safety and Tolerability of NBI-827104 in Pediatric Subjects with Epileptic Encephalopathy with Continuous Spike-and-Wave During Sleep | |||||||||||||
| Medical condition: Epileptic Encephalopathy with Continuous Spike-and-Wave During Sleep (EECSWS) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) ES (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003426-32 | Sponsor Protocol Number: DCOne-002 | Start Date*: 2017-12-11 | |||||||||||
| Sponsor Name:DCprime bv | |||||||||||||
| Full Title: AN INTERNATIONAL, MULTICENTRE, OPEN-LABEL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF TWO DIFFERENT VACCINATION REGIMENS OF IMMUNOTHERAPY WITH ALLOGENEIC DENDRITIC CELLS, DCP-001, IN PATIENTS WIT... | |||||||||||||
| Medical condition: The medical condition investigated are patients with acute myeloid leukemia in complete remission with persistent minimal residual disease and as such are at high risk of relapse. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) NO (Completed) SE (Completed) FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004045-25 | Sponsor Protocol Number: GBT440-034 | Start Date*: 2018-04-17 | |||||||||||
| Sponsor Name:Global Blood Therapeutics, Inc. | |||||||||||||
| Full Title: An Open Label Extension Study of Voxelotor (GBT440) Administered Orally to Participants with Sickle Cell Disease Who Have Participated in Voxelotor Clinical Trials | |||||||||||||
| Medical condition: Sickle Cell Disease | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) NL (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000903-26 | Sponsor Protocol Number: GBT440-032 | Start Date*: 2022-02-02 | |||||||||||
| Sponsor Name:Global Blood Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Voxelotor (GBT440) in Pediatric Participants with Sickle Cell Disease (HOPE Kids 2) | |||||||||||||
| Medical condition: Sickle Cell Disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004482-89 | Sponsor Protocol Number: GBG93 | Start Date*: 2018-01-08 | ||||||||||||||||
| Sponsor Name:GBG Forschungs GmbH | ||||||||||||||||||
| Full Title: A RANDOMIZED, OPEN-LABEL, MULTI-CENTER PHASE IV STUDY EVALUATING PALBOCICLIB PLUS ENDOCRINE TREATMENT VERSUS A CHEMOTHERAPY-BASED TREATMENT STRATEGY IN PATIENTS WITH HORMONE RECEPTOR POSITIVE / HER... | ||||||||||||||||||
| Medical condition: Metastatic breast cancer. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-005037-16 | Sponsor Protocol Number: 217095 | Start Date*: 2022-05-17 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: A randomised, double-blind, parallel group Phase III study to assess the efficacy and safety of 100 mg SC depemokimab in patients with chronic rhinosinusitis with nasal polyps (CRSwNP) – ANCHOR-1 (... | |||||||||||||
| Medical condition: Chronic Rhinosinusitis with Nasal Polyps | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) DE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002012-31 | Sponsor Protocol Number: CNTO1959PSA2003 | Start Date*: 2021-10-08 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 2a, Multicenter, Randomized, Double-blind Study Evaluating the Efficacy and Safety of Subcutaneously Administered Guselkumab and Golimumab Combination Therapy in Participants with Active Ps... | |||||||||||||
| Medical condition: Active Psoriatic Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) IT (Completed) DK (Completed) HU (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003109-92 | Sponsor Protocol Number: CRFSPN004 | Start Date*: 2020-03-20 |
| Sponsor Name:Trinity College Dublin | ||
| Full Title: Ketamine as an adjunctive therapy for Major Depression (2) - a randomised controlled trial | ||
| Medical condition: Major Depression | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-000711-76 | Sponsor Protocol Number: N/A | Start Date*: 2020-07-13 | |||||||||||
| Sponsor Name:Alexander Egeberg | |||||||||||||
| Full Title: Efficacy of roflumilast in the treatment of psoriasis – a randomised controlled trial | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005712-62 | Sponsor Protocol Number: CO43613 | Start Date*: 2022-06-17 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE Ib/II, OPEN-LABEL, MULTICENTER, RANDOMIZED UMBRELLA STUDY EVALUATING THE EFFICACY AND SAFETY OF MULTIPLE TREATMENT COMBINATIONS IN PATIENTS WITH LOCALLY ADVANCED SQUAMOUS CELL CARCINOMA OF... | |||||||||||||
| Medical condition: Squamous cell carcinoma of the head and neck | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001137-41 | Sponsor Protocol Number: 666 | Start Date*: 2018-06-26 |
| Sponsor Name:Hvidovre Hospital. Dep of Respiratory Medicine | ||
| Full Title: Use of Omalizumab will increase the pregnancy rate, proof of concept study, where women with asthma and infertility will be treated three times with weight and IgE balanced dosis at the sixth day o... | ||
| Medical condition: infertility within female asthma patients as a result of systemic inflamation. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-005331-78 | Sponsor Protocol Number: ACT16849 | Start Date*: 2022-09-06 | ||||||||||||||||
| Sponsor Name:Sanofi-Aventis Recherche & Développement | ||||||||||||||||||
| Full Title: A Phase 2 non-randomized, open-label, multi-cohort, multi center study assessing the clinical benefit of SAR444245 (THOR-707) combined with other anticancer therapies for the treatment of participa... | ||||||||||||||||||
| Medical condition: Pleural mesothelioma Non-small cell lung cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) ES (Prematurely Ended) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2022-000260-22 | Sponsor Protocol Number: PKM16982 | Start Date*: 2025-07-18 | |||||||||||
| Sponsor Name:Sanofi-Aventis Recherche & Developpement | |||||||||||||
| Full Title: A multi-center, single-arm study to investigate the pharmacokinetics and safety of dupilumab in male and female participants ≥2 years to <12 years of age with uncontrolled chronic spontaneous urti... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002150-91 | Sponsor Protocol Number: ACT16941 | Start Date*: 2022-01-31 | ||||||||||||||||
| Sponsor Name:Sanofi-Aventis Recherche & Développement | ||||||||||||||||||
| Full Title: Phase 2 non-randomized, open-label, multi-cohort, multicenter study assessing the clinical benefit of SAR444245 (THOR-707) with or without other anticancer therapies for the treatment of adults and... | ||||||||||||||||||
| Medical condition: Classic Hodgkin Lymphoma Diffuse large B-cell lymphoma | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-002123-11 | Sponsor Protocol Number: HUIS-04-2020 | Start Date*: 2020-05-07 | |||||||||||
| Sponsor Name:Tatiana Cobo Ibáñez [...] | |||||||||||||
| Full Title: EFFICACY OF CYCLOSPORINE IN THE TREATMENT OF COVID-19 PNEUMONIA: A RANDOMIZED CONTROLLED TRIAL. | |||||||||||||
| Medical condition: COVID-19 PNEUMONIA | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
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