- Trials with a EudraCT protocol (12,155)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12,155 result(s) found for: 11.
Displaying page 299 of 608.
| EudraCT Number: 2019-004987-23 | Sponsor Protocol Number: RAS-Triplet | Start Date*: 2020-05-22 |
| Sponsor Name:UMC Utrecht | ||
| Full Title: A Dose-Escalating Phase I/II Study in Patients with RAS-Mutated Metastatic Colorectal Cancer to Investigate Safety and Clinical Activity of the Triple Combination of: MEK-inhibitor binimetinib, Pan... | ||
| Medical condition: colorectal cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-003926-18 | Sponsor Protocol Number: MITO28/MANGOOV4 | Start Date*: 2018-11-19 | ||||||||||||||||
| Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | ||||||||||||||||||
| Full Title: A phase II clinical trial of Pembrolizumab in combination with Carboplatin-Paclitaxel in patients with advanced (stage III B-C-IV) ovarian, primary peritoneal and fallopian tube cancer: MITO28/MANG... | ||||||||||||||||||
| Medical condition: advanced (stage III B-C-IV) ovarian, primary peritoneal and fallopian tube cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-000309-21 | Sponsor Protocol Number: PREDICT_Trial_Amd_04 | Start Date*: 2013-10-01 | |||||||||||
| Sponsor Name:Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico | |||||||||||||
| Full Title: Antibiotic Prophylaxis and Renal Damage In Congenital abnormalities of the kidney and urinary Tract | |||||||||||||
| Medical condition: Infants with vesicoureteral reflux grade III-V, started before the first symptomatic infection. | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) LT (Completed) ES (Ongoing) DE (Ongoing) SE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001032-22 | Sponsor Protocol Number: AGI-134.FIM.101 | Start Date*: 2019-01-21 |
| Sponsor Name:Agalimmune Ltd. | ||
| Full Title: A phase I/IIa, multicentre, open label study designed to evaluate the safety and tolerability of escalating doses of AGI-134 in unresectable/metastatic solid tumours. | ||
| Medical condition: metastatic unresectable solid tumours | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-002330-23 | Sponsor Protocol Number: 9794 | Start Date*: 2017-11-24 | |||||||||||
| Sponsor Name:University hospital of Montpellier | |||||||||||||
| Full Title: HEPATIC ARTERIAL INFUSION OF GEMCITABINE-OXALIPLATIN FOR SECOND-LINE THERAPY IN NON-METASTATIC UNRESECTABLE INTRA-HEPATIC CHOLANGIOCARCINOMA: A MULTICENTRIC SINGLE-ARM PHASE II STUDY | |||||||||||||
| Medical condition: The combination of gemcitabine and oxaliplatin intra-arterial as second-line therapy can greatly improve the Objective Response Disorder (ORT) at 4 months | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000417-37 | Sponsor Protocol Number: ARRAY-818-202 | Start Date*: 2019-07-16 | |||||||||||
| Sponsor Name:Array BioPharma Inc. | |||||||||||||
| Full Title: A Phase 2, Open-label Study of Encorafenib + Binimetinib in Patients with BRAF V600E-mutant Non-small Cell Lung Cancer | |||||||||||||
| Medical condition: BRAF V600E-mutant Non-small Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003151-21 | Sponsor Protocol Number: INT 35/06 | Start Date*: 2006-08-31 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: Study to compare the tolerability of slow release oxycodone versus slow release morphine in the treatment of severe cancer pain. The study is geared towards a clinical practice improvement. | |||||||||||||
| Medical condition: Advanced cancer patient with severe cancer pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022486-10 | Sponsor Protocol Number: MT-102-2001 | Start Date*: 2010-11-02 | |||||||||||
| Sponsor Name:Myotec Therapeutics Limited | |||||||||||||
| Full Title: A multicentre, randomised, double-blind, placebo-controlled, dose-finding phase II study to evaluate the efficacy of two different doses of MT-102 administered over a sixteen week period in subject... | |||||||||||||
| Medical condition: Cachexia related to stage III and IV non-small cell lung cancer and colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Ongoing) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004076-13 | Sponsor Protocol Number: 5 | Start Date*: 2006-11-28 |
| Sponsor Name:Huvud- hals- lung- och hudcancer, Tema Cancer Karolinska Universitetssjukhuset | ||
| Full Title: Secar I Part I: A study of MTD of Sodium selenite in patients with advanced carcinoma. A phase I study. Amendment 5: continuous treatment | ||
| Medical condition: Patients with stage III or IV cancer in whom first and second line treatment have been given but who have tumours that are still progressing, giving symptomes. The patients must be in a fairly good... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004751-23 | Sponsor Protocol Number: CA2099TT | Start Date*: 2018-11-05 |
| Sponsor Name:AMC | ||
| Full Title: A Phase 1b-2 study of Mitomycin-C / Capecitabine chemoradiotherapy combined with Ipilumimab and Nivolumab or Nivolumab monotherapy as bladder sparing curative treatment for muscle Invasive bladder... | ||
| Medical condition: Muscle invasive non-metastatic bladder cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004311-40 | Sponsor Protocol Number: TORCH | Start Date*: 2018-05-24 | |||||||||||
| Sponsor Name:Academic Medical Center | |||||||||||||
| Full Title: Tranexamic Acid to Prevent Operation in Chronic Subdural Hematoma | |||||||||||||
| Medical condition: Chronic Subdural Hematoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-006004-16 | Sponsor Protocol Number: 03PDE2020 | Start Date*: 2021-07-16 |
| Sponsor Name:Celon Pharma S.A. | ||
| Full Title: Phase II, Double blind, Randomized, Placebo controlled, Parallel group, Trial to Explore the Potential Anti-dyskinetic Properties of CPL500036 (PDE10A inhibitor) in Patients with Parkinson's Diseas... | ||
| Medical condition: Levodopa-induced dyskinesia in Parkinson's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: PL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004758-39 | Sponsor Protocol Number: ESR-18-13485 | Start Date*: 2019-06-12 | |||||||||||
| Sponsor Name:AZIENDA UNITÀ SANITARIA LOCALE DELLA ROMAGNA | |||||||||||||
| Full Title: A PHASE II STUDY OF CAPECITABINE PLUS CONCOMITANT RADIATION THERAPY FOLLOWED BY DURVALUMAB (MEDI4736) AS PREOPERATIVE TREATMENT IN RECTAL CANCER | |||||||||||||
| Medical condition: Locally advanced (T3-4 N0-1) rectal cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002495-34 | Sponsor Protocol Number: GETUG 17/0702 | Start Date*: 2007-09-25 | |||||||||||
| Sponsor Name:FNCLCC | |||||||||||||
| Full Title: Etude randomisée multicentrique comparant une radiothérapie adjuvante immédidate associée à une hormonothérapie courte par analogue LH-RH (Décapeptyl LP®) vs une radiothérapie différée à la rechut... | |||||||||||||
| Medical condition: L’étude s’adresse aux patients opérés par prostatectomie radicale pour un cancer de prostate pT3 R1 pN0 ou pNx et avec un PSA post-opératoire indosable. Elle vise à comparer l’efficacité sur la sur... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000652-28 | Sponsor Protocol Number: AIEOP_LAM_2013 | Start Date*: 2015-02-04 | |||||||||||
| Sponsor Name:A.I.E.O.P. | |||||||||||||
| Full Title: Study Protocol LAM 2013/01 | |||||||||||||
| Medical condition: pediatric patient with acute myeloid leukemia | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000987-14 | Sponsor Protocol Number: TRAMANT-01 | Start Date*: 2017-10-20 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA PER L'EMERGENZA CANNIZZARO | |||||||||||||
| Full Title: Phase II Study: Maintenance therapy with Trabectedin after combination therapy Liposomal Doxorubicin plus Trabectedin vs Liposomal Doxorubicin plus Trabectedin in patients affected by relapsed ovar... | |||||||||||||
| Medical condition: Ovarian cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-003235-23 | Sponsor Protocol Number: RBM 04-34 | Start Date*: 2009-01-09 | |||||||||||
| Sponsor Name:Inserm | |||||||||||||
| Full Title: Essai randomisé multicentrique de phase II d'évaluation immunologique d'une stratégie vaccinale de type "prime boost" associant une administration du vaccin conjugué anti-pneumococcique à S0 suivie... | |||||||||||||
| Medical condition: Déficit immunitaire commun variable | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002526-23 | Sponsor Protocol Number: CS2514-2017-0004 | Start Date*: 2019-05-07 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Entasis Therapeutics | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Randomized, Active-Controlled Study to Evaluate the Efficacy and Safety of Intravenous Sulbactam-ETX2514 in the Treatment of Patients With Infections Caused by Acinetobacter baumannii-calcoacetic... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Infections Caused by Acinetobacter baumannii-calcoaceticus Complex | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: HU (Completed) LT (Completed) GR (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-004868-57 | Sponsor Protocol Number: UC-0105/1815 | Start Date*: 2019-09-02 | |||||||||||
| Sponsor Name:UNICANCER | |||||||||||||
| Full Title: Phase 2, Open label Study of DS-8201a, an Anti-HER2-AntIbody Drug Conjugate (ADC) for advanced BreaSt Cancer patients, with biomarkers analysis to characterize response/resistance to therapY | |||||||||||||
| Medical condition: Adult patients with advanced breast cancer after at least a first line of chemotherapy in metastatic setting: -if HER2 IHC3+ or IHC2+/ISH+ resistant to trastuzumab and TDM-1 -if HER2 IHC0+ or IHC... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-001780-27 | Sponsor Protocol Number: HTA-HG5-04 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Holostem Terapie Avanzate s.r.l. | |||||||||||||
| Full Title: OPEN-LABEL, UNCONTROLLED, CLINICAL TRIAL TO EVALUATE THE SAFETY AND EFFICACY OF AUTOLOGOUS FIBRIN-CULTURED EPIDERMAL GRAFTS CONTAINING EPIDERMAL STEM CELLS GENETICALLY MODIFIED FOR RESTORATION OF E... | |||||||||||||
| Medical condition: Inherited Epidermolysis Bullosa (EB) is a group of rare, devastating genetic disorders characterized by structural and mechanical fragility of skin and mucosal membranes, impairing the patient’s qu... | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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