- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,380 result(s) found.
Displaying page 1,809 of 2,219.
| EudraCT Number: 2014-002632-14 | Sponsor Protocol Number: ODYSSEY(PENTA20) | Start Date*: 2016-03-21 | |||||||||||
| Sponsor Name:Fondazione PENTA ONLUS | |||||||||||||
| Full Title: A randomised trial of dolutegravir (DTG)-based antiretroviral therapy vs. standard of care (SOC) in children with HIV infection starting first-line or switching to second-line ART | |||||||||||||
| Medical condition: Paediatric HIV infection | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) DE (Completed) PT (Completed) FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-003925-23 | Sponsor Protocol Number: PIANISSIMO | Start Date*: 2023-04-12 |
| Sponsor Name:Vrije Universiteit Brussel | ||
| Full Title: Pain medication tapering for patients with Persistent Spinal Pain Syndrome Type II, treated with Spinal Cord Stimulation. | ||
| Medical condition: Persistent spinal pain syndrome type 2 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-002821-28 | Sponsor Protocol Number: ET20-128 | Start Date*: 2020-12-24 |
| Sponsor Name:Centre Léon Bérard | ||
| Full Title: RAR-Immune: A randomised, comparative, prospective, multicentre study of the efficacy of nivolumab + ipilimumab versus pazopanib alone in patients with metastatic or unresectable advanced sarcoma o... | ||
| Medical condition: Metastatic or unresectable advanced rare sarcomas | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002329-39 | Sponsor Protocol Number: RE06 | Start Date*: 2018-01-08 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: Renal Adjuvant MultiPle Arm Randomised Trial (RAMPART): An international investigator-led phase III multi-arm multi-stage randomised controlled platform trial of adjuvant therapy in patients with r... | |||||||||||||
| Medical condition: Renal Cell Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001013-16 | Sponsor Protocol Number: PRODIGE69 | Start Date*: 2020-07-20 |
| Sponsor Name:CHU DIJON | ||
| Full Title: FOLFIRINOX VERSUS PLATINUM - ETOPOSIDE AS FIRST LINE CHEMOTHERAPY FOR METASTATIC GRADE 3 POORLY DIFFERENTIATED NEUROENDOCRINE CARCINOMA OF GASTRO ENTERO PANCREATIC AND UNKNOWN PRIMARY ASSOCIATED WI... | ||
| Medical condition: METASTATIC GRADE 3 POORLY DIFFERENTIATED NEUROENDOCRINE CARCINOMA OF GASTRO ENTERO PANCREATIC AND UNKNOWN PRIMARY | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-000729-35 | Sponsor Protocol Number: PRODIGE33-BALLAD | Start Date*: 2015-06-16 |
| Sponsor Name:Centre Hospitalier Universitaire (CHU) de Dijon | ||
| Full Title: BALLAD - A TRIAL TO EVALUATE THE POTENTIAL BENEFIT OF ADJUVANT CHEMOTHERAPY FOR SMALL BOWEL ADENOCARCINOMA | ||
| Medical condition: SMALL BOWEL ADENOCARCINOMA | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001838-19 | Sponsor Protocol Number: KER050-MD-201 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Keros Therapeutics, Inc. | ||||||||||||||||||
| Full Title: A Phase 2, Open-Label, Ascending Dose Study of KER-050 for the Treatment of Anemia in Patients with Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes (MDS) | ||||||||||||||||||
| Medical condition: Anemia in Patients with Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes (MDS). | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-000628-14 | Sponsor Protocol Number: ISS20109714 | Start Date*: 2013-09-13 | |||||||||||
| Sponsor Name:Turku University Hospital | |||||||||||||
| Full Title: Denosumab in enhancement of bone bonding of hip prosthesis in postmenopausal women: a randomized, double-blind, placebo-controlled study | |||||||||||||
| Medical condition: Hip osteoarthritis | |||||||||||||
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| Population Age: Elderly | Gender: Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000341-14 | Sponsor Protocol Number: 42847922MDD3005 | Start Date*: 2020-08-28 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Double-Blind, Randomized, Parallel-Group Study with Quetiapine Extended Release as Comparator to Evaluate the Efficacy and Safety of Seltorexant 20 mg as Adjunctive Therapy to Antidepressants in ... | |||||||||||||
| Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) GB (GB - no longer in EU/EEA) LT (Completed) LV (Completed) BE (Completed) BG (Completed) PL (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2024-000101-32 | Sponsor Protocol Number: A6281323 | Start Date*: 2024-09-19 |
| Sponsor Name:Pfizer, Inc. | ||
| Full Title: A PHASE 3 MULTICENTER, OPEN LABEL, MULTI COHORT STUDY TO EVALUATE THE EFFICACY AND SAFETY OF SOMATROPIN IN JAPANESE PARTICIPANTS WITH PRADER-WILLI SYNDROME (PWS) | ||
| Medical condition: Prader-Willi Syndrome | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2019-003710-13 | Sponsor Protocol Number: Pro-Tac | Start Date*: Information not available in EudraCT |
| Sponsor Name:University Hospital Essen | ||
| Full Title: A multi-center interventional study to assess pharmacokinetics, effectiveness and tolerability of prolonged-release Tacrolimus after Paediatric Kidney Transplantation | ||
| Medical condition: Caucasian paediatric kidney transplant recipients | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003685-40 | Sponsor Protocol Number: GFM-DACORAL-DLI | Start Date*: 2020-12-28 | ||||||||||||||||
| Sponsor Name:Groupe Francophone des Myélodysplasies (GFM) | ||||||||||||||||||
| Full Title: A PHASE II PROSPECTIVE STUDY “GFM-DACORAL-DLI” ASTX727 AND DONOR LYMPHOCYTE INFUSIONS (DLI) AFTER ALLOGENEIC STEM CELL TRANSPLANTATION (ALLO SCT) IN VERY HIGH RISK MDS OR AML PATIENTS | ||||||||||||||||||
| Medical condition: Patients with high risk myelodysplastic syndrome or acute myeloid leukemia | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-004602-59 | Sponsor Protocol Number: IFM2020-05-BENEFIT | Start Date*: 2020-11-25 | |||||||||||
| Sponsor Name:CHU DE POITIERS | |||||||||||||
| Full Title: Multicenter Open label Phase 3 study of Isatuximab plus Lenalidomide and Dexamethasone with/without Bortezomib in the Treatment of Newly diagnosed Non Frail transplant Ineligible Multiple Myeloma e... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001019-22 | Sponsor Protocol Number: KAT-PAD101 | Start Date*: 2012-10-26 | |||||||||||
| Sponsor Name:A.I.Virtanen Insitute, University of Kuopio | |||||||||||||
| Full Title: Treatment of chronic critical lower limb ischemia with combination of surgical bypass operation and adenoviral VEGF-DdNdC intramuscular gene transfer A Randomized Single-Blinded Placebo-control... | |||||||||||||
| Medical condition: Critical Chronic lower limb ischemia | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000189-31 | Sponsor Protocol Number: PRI04/2016 | Start Date*: 2017-05-12 |
| Sponsor Name:Pannon Reprodukciós Intézet B.1.2 | ||
| Full Title: Optimization and Safety Testing of Hormone Normalization Therapy in Advanced Maternal Age Infertile Women | ||
| Medical condition: The therapy is intended to treat infertility that is caused by declining egg quality that occurs with advanced maternal age. The purpose of this pilot trial is to optimize the therapeutic protocol.... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: HU (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-003865-39 | Sponsor Protocol Number: WSG-AM12 | Start Date*: 2023-05-04 | ||||||||||||||||
| Sponsor Name:Westdeutsche Studiengruppe GmbH | ||||||||||||||||||
| Full Title: NeoAdjuvant Dynamic marker - Adjusted Personalized Therapy comparing trastuzumab-deruxtecan versus pacli-/docetaxel+carboplatin+trastuzumab+pertuzumab in HER2+ early breast cancer | ||||||||||||||||||
| Medical condition: HER2+ early breast cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-005992-10 | Sponsor Protocol Number: 156-201-00307 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
| Full Title: A Phase 3b Multicenter Open-label Trial of the Safety, Tolerability, and Efficacy of Tolvaptan in Infants and Children 28 days to less than 18 years of Age with Autosomal Recessive Polycystic Kidne... | |||||||||||||
| Medical condition: Autosomal Recessive Polycystic Kidney Disease (ARPKD) | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000954-86 | Sponsor Protocol Number: 107CS-5 | Start Date*: 2020-08-17 | ||||||||||||||||
| Sponsor Name:Daehwa Pharmaceutical Co., Ltd. | ||||||||||||||||||
| Full Title: A Multinational, Multicenter, Open-label, Phase II/III Clinical Trial to Evaluate the Efficacy and Safety of Oral Paclitaxel (DHP107) Compared to IV Paclitaxel as First-line Therapy in Patients wit... | ||||||||||||||||||
| Medical condition: Recurrent or metastatic HER2 negative Breast Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Trial now transitioned) BG (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-004829-82 | Sponsor Protocol Number: GHREDECIDE | Start Date*: 2019-04-16 |
| Sponsor Name:Linköping University | ||
| Full Title: Effects of the appetite-inducing hormone ghrelin on decision making in healthy volunteers | ||
| Medical condition: NA, healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004706-22 | Sponsor Protocol Number: ImlifidARDSe.01 | Start Date*: 2023-02-17 | ||||||||||||||||||||||||||
| Sponsor Name:Charité - Universitätsmedizin Berlin | ||||||||||||||||||||||||||||
| Full Title: Imlifidase in ANCA-associated vasculitis | ||||||||||||||||||||||||||||
| Medical condition: Anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis with severe diffuse alveolar hemorrhage | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
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