- Trials with a EudraCT protocol (10,996)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (123)
10,996 result(s) found for: An Open-.
Displaying page 533 of 550.
EudraCT Number: 2017-001236-19 | Sponsor Protocol Number: CC-92480-MM-001 | Start Date*: 2018-02-13 | ||||||||||||||||
Sponsor Name:Celgene Corporation | ||||||||||||||||||
Full Title: A Phase 1/2 Multicenter, Open-label Study to Assess the Safety, Pharmacokinetics and Efficacy of CC-92480 Monotherapy and in Combination with Dexamethasone in Subjects with Relapsed and Refractory ... | ||||||||||||||||||
Medical condition: Relapsed and refractory multiple myeloma (RRMM) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) FI (Completed) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) GR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002835-27 | Sponsor Protocol Number: ION-682884-CS2 | Start Date*: 2020-03-04 | |||||||||||
Sponsor Name:Ionis Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3 Global, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ION-682884 in Patients with Transthyretin-Mediated Amyloid Cardiomyopathy (ATTR CM) | |||||||||||||
Medical condition: Transthyretin-Mediated Amyloid Cardiomyopathy (ATTR CM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Ongoing) PT (Trial now transitioned) AT (Trial now transitioned) DK (Trial now transitioned) BE (Trial now transitioned) GR (Trial now transitioned) FR (Trial now transitioned) CZ (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022620-77 | Sponsor Protocol Number: AB10006 | Start Date*: 2013-07-15 | |||||||||||||||||||||
Sponsor Name:AB Science | |||||||||||||||||||||||
Full Title: A prospective, multicentre, open-label, randomised, uncontrolled, phase 1/2 study to evaluate efficacy and safety of masitinib in combination with etoposide, or masitinib in combination with irinot... | |||||||||||||||||||||||
Medical condition: hepatocellular carcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) ES (Completed) SK (Prohibited by CA) CZ (Completed) GR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003291-12 | Sponsor Protocol Number: SHP611-201 | Start Date*: 2019-04-11 | |||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc. | |||||||||||||
Full Title: A Global, Multicenter, Open-label, Matched Historical Control Study of Intrathecal SHP611 in Subjects with Late Infantile Metachromatic Leukodystrophy | |||||||||||||
Medical condition: Late Metachromatic Leukodystrophy (MLD) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) NL (Completed) ES (Trial now transitioned) BE (Trial now transitioned) DE (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003369-37 | Sponsor Protocol Number: D9077C00001 | Start Date*: 2022-04-14 | |||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||
Full Title: A Phase II Open-label, Multicentre, Randomised Study of Neoadjuvant and Adjuvant Treatment in Patients with Resectable, Early-stage (II to IIIA) Non-small Cell Lung Cancer (NeoCOAST-2) | |||||||||||||||||||||||
Medical condition: Resectable, Early-stage (II to IIIA) Non-small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) PT (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005431-23 | Sponsor Protocol Number: MNA-3521-014-RNDZ | Start Date*: 2022-03-31 | ||||||||||||||||||||||||||
Sponsor Name:MiNA Alpha Limited | ||||||||||||||||||||||||||||
Full Title: AN OPEN LABEL, RANDOMISED, PHASE 2 STUDY TO EVALUATE THE SAFETY AND EFFICACY OF MTL-CEBPA ADMINISTERED IN COMBINATION WITH SORAFENIB OR SORAFENIB ALONE, IN TKI NAÏVE PARTICIPANTS WITH PREVIOUSLY TR... | ||||||||||||||||||||||||||||
Medical condition: Advanced hepatocellular cancer (HCC) as result of hepatitis B and/or hepatitis C | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: AT (Prematurely Ended) FR (Completed) BE (Prematurely Ended) SE (Prematurely Ended) NL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005173-20 | Sponsor Protocol Number: MEDI4736-DLBCL-001 | Start Date*: 2016-12-21 | |||||||||||
Sponsor Name:Celgene International II Sàrl | |||||||||||||
Full Title: A Phase 2, Open-label, Multicenter Study to Evaluate the Safety and Clinical Activity of Durvalumab in Combination with Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisone (R-CHOP) or... | |||||||||||||
Medical condition: Previously untreated, high-risk diffuse-large B-cell lymphoma (DLBCL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DK (Prematurely Ended) EE (Completed) SK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000212-28 | Sponsor Protocol Number: LOXO-RET-18036 | Start Date*: 2020-04-15 | ||||||||||||||||||||||||||
Sponsor Name:Loxo Oncology, Inc. | ||||||||||||||||||||||||||||
Full Title: A Phase 1/2 Study of the Oral RET Inhibitor LOXO-292 in Pediatric Patients with Advanced RET-Altered Solid or Primary Central Nervous System Tumors | ||||||||||||||||||||||||||||
Medical condition: Pediatric Patients with Advanced RET-Altered Solid or Primary Central Nervous System Tumors | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) DE (Trial now transitioned) DK (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002774-27 | Sponsor Protocol Number: DS1062-A-U202 | Start Date*: 2021-04-16 | |||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
Full Title: Phase 2, Single-arm, Open-label Study of DS-1062a in Advanced or Metastatic Non-small Cell Lung Cancer with Actionable Genomic Alterations and Progressed on or After Applicable Targeted Therapy an... | |||||||||||||
Medical condition: Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Trial now transitioned) HU (Completed) NL (Trial now transitioned) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002792-42 | Sponsor Protocol Number: RV-FOL-GELARC-0683 | Start Date*: 2012-07-17 | |||||||||||||||||||||
Sponsor Name:LYSARC | |||||||||||||||||||||||
Full Title: A phase 3 open label randomized study to compare the efficacy and safety of rituximab plus lenalidomide ( CC-5013) versus rituximab plus chemotherapy followed by rituximab in subjects with previous... | |||||||||||||||||||||||
Medical condition: stage II-IV follicular lymphoma grade 1-3a not previously treated | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) IT (Completed) DE (Completed) PT (Completed) ES (Ongoing) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002053-33 | Sponsor Protocol Number: TV48125CNS30082 | Start Date*: 2021-01-07 | ||||||||||||||||
Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Comparing the Efficacy, Safety, and Tolerability of Subcutaneous Administration of Fremanezumab Versus Placebo for ... | ||||||||||||||||||
Medical condition: Chronic Migraine | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) FI (Completed) NL (Completed) PL (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-003124-41 | Sponsor Protocol Number: 219510 | Start Date*: 2023-03-27 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals SA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 3b, non-randomized, open label, multi-country, cohort study to describe the safety of study participants who received RSVPreF3 maternal vaccination (any dose) or controls from previous RSV ... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Pregnancy related outcomes and events in maternal participants who were vaccinated against RSV or received control, and in their infants | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) BE (Completed) DE (Completed) FR (Ongoing) ES (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003625-34 | Sponsor Protocol Number: 1311.5 | Start Date*: 2016-04-13 | |||||||||||
Sponsor Name:Boehringer Ingelheim Finland Ky | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, proof-of-concept, dose-ranging study of BI 655066 / ABBV-066 / risankiumab in patients with active psoriatic arthritis | |||||||||||||
Medical condition: Active Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) ES (Completed) NL (Completed) DE (Completed) BE (Completed) CZ (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022207-22 | Sponsor Protocol Number: H9B-MC-BCDV | Start Date*: 2011-06-08 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double Blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of LY2127399 in Patients with Moderate to Severe Rheumatoid Arthritis (RA) who had an ... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Completed) GR (Prematurely Ended) IT (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002912-10 | Sponsor Protocol Number: CH-ACM-01 | Start Date*: 2011-08-31 | |||||||||||
Sponsor Name:Chiasma, Inc. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ORAL OCTREOLIN™ IN PATIENTS WITH ACROMEGALY WHO ARE CURRENTLY RECEIVING PARENTERAL SOMATOSTATIN ANALOGS | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) NL (Completed) GB (Completed) DE (Completed) SK (Completed) PL (Completed) IT (Completed) SI (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015595-10 | Sponsor Protocol Number: IC51-322 | Start Date*: 2010-03-23 | |||||||||||||||||||||||||||||||
Sponsor Name:Intercell AG | |||||||||||||||||||||||||||||||||
Full Title: IMMUNOGENICITY AND SAFETY OF THE JAPANESE ENCEPHALITIS VACCINE IC51 (IXIARO®, JESPECT®) IN A PEDIATRIC POPULATION IN NON‐ENDEMIC COUNTRIES. UNCONTROLLED, OPEN‐LABEL PHASE 3 STUDY | |||||||||||||||||||||||||||||||||
Medical condition: Japanese Encephalitis (JE) | |||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) DK (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001662-42 | Sponsor Protocol Number: 20120249 | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Double-blind, Multi-center Phase 2 Trial of Denosumab in Combination With Chemotherapy as First-line Treatment of Metastatic Non-small Cell Lung Cancer | |||||||||||||
Medical condition: Non-small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) IT (Completed) GB (Completed) GR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004461-41 | Sponsor Protocol Number: CR-AIR-007 | Start Date*: 2013-06-27 | |||||||||||||||||||||||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | |||||||||||||||||||||||||||||||||
Full Title: An exploratory, open-label, multicenter study to evaluate the safety and efficacy of ATIR, donor T-lymphocytes depleted ex vivo of host alloreactive T-cells, in patients with a hematologic malignan... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with a hematologic malignancy (AML, ALL, or MDS) who are eligible for a haploidentical HSCT | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004076-34 | Sponsor Protocol Number: 7487-CL-0209 | Start Date*: 2014-02-27 | ||||||||||||||||||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. | ||||||||||||||||||||||||||||
Full Title: A phase II open-label rollover study for subjects that have participated in an Astellas sponsored linsitinib trial | ||||||||||||||||||||||||||||
Medical condition: Solid tumors | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CZ (Completed) PL (Completed) GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016858-41 | Sponsor Protocol Number: E7080-G000-204 | Start Date*: 2010-10-05 | ||||||||||||||||||||||||||
Sponsor Name:Eisai Ltd. | ||||||||||||||||||||||||||||
Full Title: An Open-Label, Single-Arm, Multicenter Phase 2 Study of E7080 in Subjects with Advanced Endometrial Cancer and Disease Progression Following First-Line Chemotherapy | ||||||||||||||||||||||||||||
Medical condition: Unresectable endometrial cancer and disease progression following platinum-based, first-line chemotherapy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: HU (Completed) BG (Completed) BE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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