- Trials with a EudraCT protocol (44,341)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,341 result(s) found.
Displaying page 1,778 of 2,218.
EudraCT Number: 2022-002485-32 | Sponsor Protocol Number: CTRIAL-IE-22-01 | Start Date*: 2023-03-07 | |||||||||||
Sponsor Name:Cancer Trials Ireland | |||||||||||||
Full Title: Single arm phase 2 trial of neoadjuvant trastuzumab deruxtecan (T-DXd) with response-directed definitive therapy in early stage HER2-positive breast cancer: a standard chemotherapy-sparing approach... | |||||||||||||
Medical condition: HER2-positive breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003188-24 | Sponsor Protocol Number: CA184-587 | Start Date*: 2020-11-13 | |||||||||||
Sponsor Name:Sahlgrenska University Hospital | |||||||||||||
Full Title: A Phase I Randomized Controlled Multicentre Trial of Isolated Hepatic Perfusion in Combination with Ipilimumab and Nivolumab in Patients with Uveal Melanoma Metastases | |||||||||||||
Medical condition: Metastatic uveal melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000375-25 | Sponsor Protocol Number: BotA-KKDS2016 | Start Date*: 2016-04-19 |
Sponsor Name:Danderyds sjukhus AB | ||
Full Title: Double blind placebo-controlled RCT of the efficacy and safety of intramuscular injections of Botulinum Toxin A as a treatment for provoked vestibulodynia | ||
Medical condition: Provoked vestibulodynia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019635-36 | Sponsor Protocol Number: 2010-001 | Start Date*: 2010-05-04 | |||||||||||
Sponsor Name:Aker BioMarine Antarctic AS | |||||||||||||
Full Title: A Single Centre, Open-Label, Randomised Multi-Dose Study to Assess Changes in the Brain Metabolism of Juvenile ADHD Patients After Thirteen Weeks of Daily Intake of 4 g Superba Krill Oil or 4 g ome... | |||||||||||||
Medical condition: Attention deficit/hyperactivity disorder | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016094-16 | Sponsor Protocol Number: AGO/2009/008 | Start Date*: 2010-02-04 | |||||||||||
Sponsor Name:University Hospital Ghent | |||||||||||||
Full Title: Sevoflurane-Remifentanil interaction: Multiple response surfaces, validation of calibration stimuli, validation of the intraoperative isobole concept and investigating remifentanil induced opioid t... | |||||||||||||
Medical condition: American Society of Anesthesia class I and II patients scheduled for surgery under general anesthesia. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008202-52 | Sponsor Protocol Number: REMARC | Start Date*: 2009-09-14 | |||||||||||
Sponsor Name:LYSARC | |||||||||||||
Full Title: DOUBLE BLIND RANDOMIZED PHASE III STUDY OF LENALIDOMIDE (REVLIMID®) MAINTENANCE VERSUS PLACEBO IN RESPONDING ELDERLY PATIENTS WITH DLBCL AND TREATED WITH R-CHOP IN FIRST LINE | |||||||||||||
Medical condition: Diffuse Large B Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) PT (Completed) ES (Completed) AT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003889-39 | Sponsor Protocol Number: NALPAC | Start Date*: 2021-10-11 |
Sponsor Name:Belgian Group of Digestive Oncology (BGDO) | ||
Full Title: A Non-Comparative Randomized Phase 2 Study, Evaluating the Efficacy of 5-FU + NALIRI and 5-FU + NALIRINOX for Metastatic Pancreatic Ductal Adenocarcinoma (PDAC), Progressive After Gemcitabine-Abra... | ||
Medical condition: Pancreatic ductal adenocarcinoma (PDAC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004142-11 | Sponsor Protocol Number: A011-11 | Start Date*: 2021-05-12 | |||||||||||
Sponsor Name:Acceleron Pharma Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Compare the Efficacy and Safety of Sotatercept Versus Placebo When Added to Background Pulmonary Arterial Hypertension (PAH) Therapy... | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension (PAH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) FR (Completed) BE (Completed) NL (Completed) AT (Completed) PL (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000971-26 | Sponsor Protocol Number: RHF-CAELYX-002 | Start Date*: 2016-04-04 |
Sponsor Name:Charles University in Prague, Medical Faculty | ||
Full Title: Liposoms (drug delivery systems) in kinetically guided therapy of ovarian platinum-resistant carcinoma with doxorubicin using plasmafiltration | ||
Medical condition: Chemotherapy of ovarian platinum-resistant carcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001512-65 | Sponsor Protocol Number: MEMMATCZ | Start Date*: 2012-06-19 |
Sponsor Name:Masaryk University | ||
Full Title: A Phase II study of metronomic and targeted anti-angiogenesis therapy for children with recurrent/progressive medulloblastoma | ||
Medical condition: recurrent or progressive medulloblastoma | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001419-25 | Sponsor Protocol Number: GastricCHIMERAtrial | Start Date*: 2021-04-09 | |||||||||||
Sponsor Name:Jagiellonian University Medical College | |||||||||||||
Full Title: Preoperative intraperitoneal chemotherapy in adjuvant hyperthermia adjunctive therapy in advanced gastric cancer with high-risk of peritoneal recurrence - a multicentre randomized trial | |||||||||||||
Medical condition: Gastric Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003574-16 | Sponsor Protocol Number: MK3475-059 | Start Date*: 2015-05-08 |
Sponsor Name:Merck Sharp & Dohme Corp., a Subsidiary of Merck & Co., Inc. | ||
Full Title: A Phase II Clinical Trial of Pembrolizumab as Monotherapy and in Combination with Cisplatin+5-Fluorouracil in Subjects with Recurrent or Metastatic Gastric or Gastroesophageal Junction Adenocarcino... | ||
Medical condition: Gastric Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (Completed) LT (Completed) EE (Completed) FR (Completed) RO (Temporarily Halted) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002125-19 | Sponsor Protocol Number: 9494 | Start Date*: 2016-06-20 |
Sponsor Name:CHU MontpellierCentre administratif André Benech, | ||
Full Title: A phase IIb, prospective, multicentre, double-blind, triple-arm, randomized versus placebo trial, to assess the efficacy of a single injection of either 2 or 10 x 106 autologous adipose derived mes... | ||
Medical condition: Active knee Osteoarthritis (mild to moderate) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) NL (Completed) DE (Completed) IE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002746-40 | Sponsor Protocol Number: VX22-864-108 | Start Date*: 2023-04-11 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 2, Open-label Study Evaluating Efficacy and Safety of VX-864 in Subjects With Alpha-1 Antitrypsin Deficiency Who Have the PiZZ Genotype, Over 48 Weeks | |||||||||||||
Medical condition: Alpha 1 antitrypsin deficiency in Subjects With the PiZZ Genotype | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001916-44 | Sponsor Protocol Number: MiFlaPRO_2019 | Start Date*: 2020-01-28 |
Sponsor Name:Medical University Innsbruck, Department of Visceral, Transplant und Thoracic Surgery | ||
Full Title: A multicenter, randomized, double blind placebo controlled trial of Micronized purified Flavonoid- Fraction (MPFF) in the management of radiation proctitis | ||
Medical condition: Patients with radiation proctitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-001072-11 | Sponsor Protocol Number: CO41012 | Start Date*: 2019-08-21 | ||||||||||||||||
Sponsor Name:Roche Farma S. A. U. que realiza el ensayo en España y que actúa como representante F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: A PHASE IB/III STUDY OF IPATASERTIB PLUS PALBOCICLIB AND FULVESTRANT VERSUS PLACEBO PLUS PALBOCICLIB AND FULVESTRANT IN HORMONE RECEPTOR POSITIVE AND HER2 NEGATIVE LOCALLY ADVANCED UNRESECTABLE OR ... | ||||||||||||||||||
Medical condition: Hormone receptor (HR)-positive/HER2-negative locally advanced unresectable or metastatic breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000081-15 | Sponsor Protocol Number: M19-051 | Start Date*: 2021-08-24 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Dose- Ranging Study to Evaluate the Safety and Efficacy of Upadacitinib in Subjects with Non-Segmental Vitiligo | |||||||||||||
Medical condition: Vitiligo | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004391-18 | Sponsor Protocol Number: PI2020_843_0114 | Start Date*: 2020-10-28 |
Sponsor Name:CHU Amiens-Picardie | ||
Full Title: IMPACT OF ANTI-TNF, VEDOLIZUMAB AND TOFACITINIB ON AORTIC STIFFNESS, CAROTID INTIMA-MEDIA THICKNESS AND CARDIOVASCULAR RISK OF PATIENTS WITH ULCERATIVE COLITIS | ||
Medical condition: ulcerative colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001015-23 | Sponsor Protocol Number: APHP180668 | Start Date*: 2020-05-13 |
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
Full Title: Double blind, multicentric, randomized, placebo-controlled trial, evaluating the efficacy of 24-month of bezafibrate in primary sclerosing cholangitis with persistent cholestasis despite ursodeoxyc... | ||
Medical condition: Adult patients with primary sclerosing cholangitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000254-28 | Sponsor Protocol Number: RC31/19/0500 | Start Date*: 2022-05-19 | |||||||||||
Sponsor Name:University Hospital of Toulouse | |||||||||||||
Full Title: Interest of oxytocin as an adjuvant treatment of psycho-educational measures in challenging behaviors in children with autism spectrum disorders and moderate to severe intellectual disability: feas... | |||||||||||||
Medical condition: autism | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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