- Trials with a EudraCT protocol (1,413)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,413 result(s) found for: Cell body.
Displaying page 66 of 71.
| EudraCT Number: 2013-004304-19 | Sponsor Protocol Number: 117119 | Start Date*: 2015-07-23 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A Phase III, randomized, open-label, controlled, multicenter study to evaluate immunogenicity and safety of GSK Biologicals' Infanrix hexa™ vaccine when administered to healthy infants as primary v... | ||
| Medical condition: Active immunization against diphtheria, tetanus, pertussis infection caused by all known subtypes of hepatitis B virus, poliomyelitis, and invasive disease caused by Haemophilus influenzae type B (... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001159-11 | Sponsor Protocol Number: POL7080-010 | Start Date*: 2019-02-08 | |||||||||||
| Sponsor Name:Polyphor Ltd. | |||||||||||||
| Full Title: A multicenter, open-label, sponsor-blinded, randomized, active-controlled, parallel group, pivotal study to evaluate the efficacy, safety, and tolerability of murepavadin given with ertapenem versu... | |||||||||||||
| Medical condition: Nosocomial pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) FR (Prematurely Ended) LT (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003570-77 | Sponsor Protocol Number: SB010/04/2012 | Start Date*: 2012-12-04 | |||||||||||
| Sponsor Name:sterna biologicals GmbH & Co. KG | |||||||||||||
| Full Title: Clinical study to investigate safety, tolerability, efficacy, pharmacokinetics and pharmacodynamics of multiple doses of the human GATA-3-specific DNAzyme solution SB010 in patients with mild aller... | |||||||||||||
| Medical condition: The trial will be conducted in 38 male patients with mild allergic asthma and documented or known biphasic reaction to allergen challenge (AC). | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001048-40 | Sponsor Protocol Number: B1371013 | Start Date*: 2015-02-10 | |||||||||||
| Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, 10017 | |||||||||||||
| Full Title: A phase 2, double-blind, randomized safety and efficacy study of Glasdegib (PF-04449913) versus placebo in patients with Myelofibrosis previously treated with ruxolitinib. | |||||||||||||
| Medical condition: Myelofibrosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) AT (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000619-14 | Sponsor Protocol Number: GBG84 | Start Date*: 2014-11-04 |
| Sponsor Name:German Breast Group | ||
| Full Title: A randomized phase III trial comparing two dose-dense, dose-intensified approaches (ETC and PM(Cb)) for neoadjuvant treatment of patients with high-risk early breast cancer (GeparOcto) | ||
| Medical condition: Patients with primary breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-001930-93 | Sponsor Protocol Number: GC-627-04 | Start Date*: 2017-01-13 | ||||||||||||||||
| Sponsor Name:Generon (Shanghai) Corporation Ltd. | ||||||||||||||||||
| Full Title: A Phase III, Randomized, Multi-Centre, Double-Blind, Placebo Controlled Clinical Trial of F-627 in Women with Breast Cancer Receiving Myelotoxic Chemotherapy | ||||||||||||||||||
| Medical condition: Women, between 18 and 75 years of age that have been diagnosed with Stage II-IV breast cancer in the adjuvant or metastatic setting and are scheduled to undergo chemotherapy. This is a profilaxis ... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: HU (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-000828-24 | Sponsor Protocol Number: ANRS163ETRAL | Start Date*: 2015-05-31 | |||||||||||
| Sponsor Name:Inserm-ANRS | |||||||||||||
| Full Title: A non-comparative phase II trial evaluating the capacity of the dual combination raltegravir/etravirine to maintain virological success in HIV-1 infected patients of at least 45 years of age with a... | |||||||||||||
| Medical condition: HIV infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002895-42 | Sponsor Protocol Number: GITS2013_4.0 | Start Date*: 2013-10-10 | ||||||||||||||||
| Sponsor Name:Region Västerbotten | ||||||||||||||||||
| Full Title: Glaucoma Intensity Treatment Study – Intensive non-invasive glaucoma treatment vs conventional stepwise treatment – a prospective, randomized phase IV study of disease progression in glaucoma (GITS... | ||||||||||||||||||
| Medical condition: Glaucoma, open-angle and PEX glaucoma. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-000561-33 | Sponsor Protocol Number: TOL-2 | Start Date*: 2022-03-08 | |||||||||||
| Sponsor Name:TolerogenixX GmbH | |||||||||||||
| Full Title: An open, randomized-controlled, multi-center phase-II clinical trial of individualized immunosuppression with intravenously administered donor modified immune cells (MIC) compared to standard-of-ca... | |||||||||||||
| Medical condition: Living donor kidney transplantation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001244-95 | Sponsor Protocol Number: MK-3475-C11 | Start Date*: 2021-07-30 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: Phase 2 Study of Pembrolizumab and Chemotherapy in Patients With Newly Diagnosed Classical Hodgkin Lymphoma (KEYNOTE-C11) | |||||||||||||
| Medical condition: Classical Hodgkin Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) FR (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005770-26 | Sponsor Protocol Number: KRONF2 | Start Date*: 2023-10-20 | ||||||||||||||||
| Sponsor Name:Medical University of Warsaw | ||||||||||||||||||
| Full Title: Phase 2a non-commercial and non-randomized intervention study evaluating the efficacy of crizotinib in the treatment of children with severe type 2 neurofibromatosis, in particular those excluded f... | ||||||||||||||||||
| Medical condition: Neurofibromatosis type 2 is a genetically determined primary malignancy resulting from a mutation that disables the function of the cell division control gene and leads to neoplasia such as benign ... | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-003461-34 | Sponsor Protocol Number: UR1840 | Start Date*: 2019-07-09 | |||||||||||||||||||||
| Sponsor Name:Department of Oncology, Herlev & Gentofte Hospital | |||||||||||||||||||||||
| Full Title: Randomised phase 2 trial of stereotactic body radiation therapy, SBRT, in combination with checkpoint inhibitors in metastatic castration-resistant prostate cancer | |||||||||||||||||||||||
| Medical condition: metastatic castration-resistant prostate cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2018-001823-38 | Sponsor Protocol Number: AB65/18 | Start Date*: 2018-11-26 | |||||||||||
| Sponsor Name:Technische Universität München, Fakultät für Medizin vertreten durch den Dekan | |||||||||||||
| Full Title: A prospective, single arm, multicenter, phase II-trial to assess safety and efficacy of preoperative RAdiation therapy before radical CystEctomy combined with ImmunoTherapy in locally advanced urot... | |||||||||||||
| Medical condition: Locally advanced urothelial bladder cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002044-28 | Sponsor Protocol Number: HGT-MLD-070 | Start Date*: 2012-06-14 | |||||||||||
| Sponsor Name:Shire Human Genetics Therapies Inc | |||||||||||||
| Full Title: A Phase I/II, Multicenter, Open-label, Dose Escalation Study of HGT-1110 Administered Intrathecally in Children with Metachromatic Leukodystrophy | |||||||||||||
| Medical condition: Treatment of Metachromatic Leukodystrophy | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-011055-43 | Sponsor Protocol Number: GENA-08 | Start Date*: 2009-10-22 | |||||||||||
| Sponsor Name:Octapharma AG | |||||||||||||
| Full Title: Clinical Study to Investigate the Efficacy, Safety, and Immunogenicity of human-cl rhFVIII in Previously Treated Patients With Severe Haemophilia A | |||||||||||||
| Medical condition: Severe haemophilia A (FVIII:C <=1%) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003664-32 | Sponsor Protocol Number: 201301 | Start Date*: 2014-03-26 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Medical Center Alkmaar | ||||||||||||||||||||||||||||||||||||||
| Full Title: ‘Effect of omega-3 fatty acids on the perioperative immune response and erythrocyte function’ | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients undergoing colon surgery for malignancy. | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2014-005674-11 | Sponsor Protocol Number: ADVL1412 | Start Date*: 2015-04-08 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:National Cancer Institute | ||||||||||||||||||||||||||||||||||||||
| Full Title: A PHASE 1/2 STUDY OF NIVOLUMAB (IND# 124729) IN CHILDREN, ADOLESCENTS, AND YOUNG ADULTS WITH RECURRENT OR REFRACTORY SOLID TUMORS AS A SINGLE AGENT AND IN COMBINATION WITH IPILIMUMAB | ||||||||||||||||||||||||||||||||||||||
| Medical condition: •Childhood Solid Neoplasm •Recurrent Childhood Rhabdomyosarcoma •Recurrent Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor •Recurrent Neuroblastoma •Recurrent Osteosarcoma •Recurrent ... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-002073-26 | Sponsor Protocol Number: 1125-ECIR | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
| Sponsor Name:Medical Center - University of Freiburg | |||||||||||||||||||||||
| Full Title: Phase 1/2 Trial to determine the safety and efficacy of Extracorporeal photopheresis as treatment for steroid-refractory immune related adverse events after immune checkpoint inhibitor therapy | |||||||||||||||||||||||
| Medical condition: Immune related adverse events induced by treatment with immune checkpoint inhibitors (monoclocanl antibodies against PD-1, PD-L1 or CTLA-4) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2018-001238-16 | Sponsor Protocol Number: CNTO1959PSO3012 | Start Date*: 2019-01-03 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 3b, Randomized, Double-blind, Active-controlled, Multicenter Study to Evaluate Further Therapeutic Strategies with Guselkumab in Patients with Moderate-to-Severe Plaque-Type Psoriasis | |||||||||||||
| Medical condition: Moderate to Severe Plaque Type Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003418-18 | Sponsor Protocol Number: SMR2268/TheMIBSStudy | Start Date*: 2012-01-09 | |||||||||||
| Sponsor Name:Sahlgrenska University Hospital | |||||||||||||
| Full Title: A Randomised, Double Blind, Placebo Controlled, Multi-centre, Parallel Group, Interventional Study of Mesalazine (Asacol®) Treatment in IBS and the Evaluation of Rectal Inflammatory Status using th... | |||||||||||||
| Medical condition: Irritable Bowel Syndrome | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) NO (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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