- Trials with a EudraCT protocol (44,399)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,399 result(s) found.
Displaying page 1,868 of 2,220.
| EudraCT Number: 2018-003842-18 | Sponsor Protocol Number: OTL-103-4 | Start Date*: 2019-01-08 | |||||||||||
| Sponsor Name:Orchard Therapeutics Ltd. | |||||||||||||
| Full Title: A Single Arm, Open Label Clinical Study of Haematopoietic Stem Cell Gene Therapy with Cryopreserved Autologous CD34+ Cells Transduced with Lentiviral Vector encoding WAS cDNA in Subjects with Wisko... | |||||||||||||
| Medical condition: Wiskott-Aldrich Syndrome | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001588-10 | Sponsor Protocol Number: VIVA | Start Date*: 2021-09-27 | |||||||||||
| Sponsor Name:IRCCS-A.O.U. SAN MARTINO-IST | |||||||||||||
| Full Title: A randomized, phase IIb study of adjuvant durvalumab (MEDI4736) plus regorafenib vs untreated control in stage IV colorectal cancer patients with no evidence of disease (NED): VIVA trial | |||||||||||||
| Medical condition: stage IV colorectal cancer patients with no evidence of disease (NED) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001557-31 | Sponsor Protocol Number: ALKS4230-006 | Start Date*: 2022-01-31 | |||||||||||
| Sponsor Name:Alkermes, Inc. | |||||||||||||
| Full Title: A Phase 2, Open-label, Multicenter, Cohort Study of Nemvaleukin Alfa (ALKS 4230) Monotherapy Administered Subcutaneously in Patients With Advanced Cutaneous Melanoma or Intravenously in Patients Wi... | |||||||||||||
| Medical condition: Advanced cutaneous melanoma and Advanced mucosal melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-002860-29 | Sponsor Protocol Number: ONC-2019-002 | Start Date*: 2019-12-12 | |||||||||||
| Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
| Full Title: Efficacy and safety of Cabozantinib in patients with hepatocellular carcinoma progressing on or intolerant to prior treatment with immune checkpoint inhibitors: A Phase II study (Immunocabo). | |||||||||||||
| Medical condition: Hepatocellular carcinoma (HCC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005942-41 | Sponsor Protocol Number: GOIRC-05-2020 | Start Date*: 2022-01-12 | ||||||||||||||||
| Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC) | ||||||||||||||||||
| Full Title: A multicenter phase II, single arm study of Durvalumab (MEDI 4736) with Carboplatin plus Etoposide for 4 cycles followed by Durvalumab maintenance in patients with metastatic pulmonary large-cell n... | ||||||||||||||||||
| Medical condition: treatment-naïve patients with metastatic pulmonary large-cell neuroendocrine carcinoma (LCNEC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2017-002949-30 | Sponsor Protocol Number: ATA129-EBV-302 | Start Date*: 2020-07-17 | ||||||||||||||||
| Sponsor Name:Atara Biotherapeutics, Inc. | ||||||||||||||||||
| Full Title: Multicenter, Open Label, Phase 3 Study of Tabelecleucel for Solid Organ or Allogeneic Hematopoietic Cell Transplant Subjects with Epstein-Barr Virus-Associated Post-Transplant Lymphoproliferative D... | ||||||||||||||||||
| Medical condition: Epstein-Barr Virus-Associated Post-Transplant Lymphoproliferative Disease | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Trial now transitioned) ES (Ongoing) AT (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-005838-22 | Sponsor Protocol Number: CLIO | Start Date*: 2016-07-22 |
| Sponsor Name:UZLeuven | ||
| Full Title: Circulating tumor DNA guiding (Olaparib) Lynparza® treatment in Ovarian Cancer (CLIO). Establishing the value of a ctDNA-based HRD assay for predicting olaparib response in women with relapsed ovar... | ||
| Medical condition: platinum-sensitive and platinum-resistant relapsed ovarian cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000531-17 | Sponsor Protocol Number: D5160C00002 | Start Date*: 2014-05-20 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase II, Open Label, Single-arm Study to Assess the Safety and Efficacy of AZD9291 in Patients with EGFRm+/T790M+, Locally Advanced or Metastatic NSCLC who have Progressed Following Prior Therap... | |||||||||||||
| Medical condition: Non Small Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2024-000442-10 | Sponsor Protocol Number: A8081056 | Start Date*: 2024-10-11 |
| Sponsor Name:Pfizer, Inc | ||
| Full Title: CRIZOTINIB (XALKORI(REGISTERED)) EXPANDED ACCESS PROTOCOL FOR THE TREATMENT OF ADULT OR PEDIATRIC PATIENTS WITH SOLID OR HEMATOLOGIC MALIGNANCIES THAT HARBOR A CRIZOTINIB-SENSITIVE MOLECULAR ALTERA... | ||
| Medical condition: Solid tumors | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2012-005637-36 | Sponsor Protocol Number: CLDK378A2303 | Start Date*: 2013-09-30 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A phase III, multicenter, randomized, open-label study of oral LDK378 versus standard chemotherapy in adult patients with ALK-rearranged (ALK-positive) advanced non-small cell lung cancer who have ... | |||||||||||||
| Medical condition: non-small cell lung cancer (NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) ES (Ongoing) FR (Completed) NL (Completed) GB (GB - no longer in EU/EEA) IE (Completed) BE (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003218-38 | Sponsor Protocol Number: AAUH-VATS-01 | Start Date*: 2021-09-08 | |||||||||||
| Sponsor Name:Aalborg University Hospital | |||||||||||||
| Full Title: Pain after thoracoscopic lung surgery – the effect of intercostal nerve blockades with standard bupivacaine and liposomal bupivacaine – a randomised controlled feasibility trial | |||||||||||||
| Medical condition: Acute postoperative pain Lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003830-17 | Sponsor Protocol Number: ACH228-110 | Start Date*: 2020-09-16 | |||||||||||
| Sponsor Name:Achillion Pharmaceuticals, Inc., a wholly owned subsidiary of Alexion Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Phase 2 Open-Label Proof of Concept Study to Assess the Efficacy, Safety, and Pharmacokinetics of the Oral Factor D (FD) Inhibitor ACH-0145228 in Paroxysmal Nocturnal Hemoglobinuria (PNH) Patient... | |||||||||||||
| Medical condition: Paroxysmal Nocturnal Hemoglobinuria (PNH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) IT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002790-58 | Sponsor Protocol Number: CA209-74W | Start Date*: 2020-09-24 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Randomized, Multi-center, Double-blinded, Placebo-controlled Phase 3 Study of Nivolumab and Ipilimumab, Nivolumab Monotherapy, or Placebo in Combination with Trans-arterial ChemoEmbolization (TAC... | |||||||||||||
| Medical condition: Intermediate-stage Hepatocellular Carcinoma (HCC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) FR (Completed) DE (Completed) BE (Completed) CZ (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000724-34 | Sponsor Protocol Number: Nuc-STOP | Start Date*: 2018-07-02 | |||||||||||
| Sponsor Name:Oslo University Hospital HF | |||||||||||||
| Full Title: Norwegian Nucleoside Analogue Stop Study (Nuc-STOP) - A randomized open-label trial in HBeAg negative chronic hepatitis B, aiming at achieving a functional Cure | |||||||||||||
| Medical condition: HBeAg negative chronic hepatitis B | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) SE (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003837-13 | Sponsor Protocol Number: ROPPET-NAF | Start Date*: 2020-04-20 |
| Sponsor Name:Centro Hospitalar e Universitário de Coimbra, E.P.E. | ||
| Full Title: Rosuvastatin effect on atherosclerotic plaque metabolism ¿ a subclinical atherosclerosis imaging study with 18F-NaF PET-CT | ||
| Medical condition: Atherosclerosis, namely in the aorta, carotid and coronary arteries | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: PT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-003821-31 | Sponsor Protocol Number: Futurum-963747 | Start Date*: 2022-03-15 |
| Sponsor Name:Region Jönköping, Sweden [...] | ||
| Full Title: Patient-controlled Sedation in Port Implantation (PACSPI 2)- a randomized controlled trial | ||
| Medical condition: Patients ≥18 years with cancer in need of subcutaneous venous port will be offered to participate in the trial. The aim of the trial is to determine if patient-controlled sedation (PCS) with prop... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-003025-93 | Sponsor Protocol Number: P051070 | Start Date*: 2007-01-23 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Etude de la réduction des poussées de lupus érythémateux systémique par adaptation de la posologie de l'hydroxychloroquine à sa concentration sanguine. Etude randomisée multicentrique nationale. | |||||||||||||
| Medical condition: - Cette étude est indiquée chez les patients adultes ayant un diagnostic de lupus érythémateux systémique. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-007595-42 | Sponsor Protocol Number: | Start Date*: 2008-04-22 |
| Sponsor Name:Cardiac Reserch Unit | ||
| Full Title: Chest pain or other pain raising suspicion of an acute coronary syndrome. An evaluation of benzodiazipines and prehospital care. | ||
| Medical condition: This study evaluates the possibility to improve symptoms prior to hospital admission among patients suffering from acute chest pain. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002191-41 | Sponsor Protocol Number: AIDIT | Start Date*: Information not available in EudraCT |
| Sponsor Name:Uppsala University | ||
| Full Title: Azithromycin Insulin Diet Intervention Trial in Type 1 Diabetes | ||
| Medical condition: Type 1 diabetes | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-001381-15 | Sponsor Protocol Number: RICH-ART | Start Date*: 2012-06-13 | |||||||||||
| Sponsor Name:Sahlgrenska University Hospital Västra Götalandsregionen | |||||||||||||
| Full Title: Radiation Induced Cystits treated with Hyperbaric Oxygen. A Randomized controlled Trial | |||||||||||||
| Medical condition: Radiation Cystitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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