- Trials with a EudraCT protocol (2,316)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,316 result(s) found.
Displaying page 30 of 116.
| EudraCT Number: 2021-005331-23 | Sponsor Protocol Number: SCOUT-015 | Start Date*: 2022-06-20 | |||||||||||
| Sponsor Name:Radius Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 2/3, Randomized, Double-Blind, Placebo-Controlled Study of RAD011 (Cannabidiol Oral Solution) for the Treatment of Patients with Prader-Willi Syndrome | |||||||||||||
| Medical condition: Hyperphagia related behavior associated with Prader-Willi Syndrome | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002638-54 | Sponsor Protocol Number: ALN-AS1-002 | Start Date*: 2017-12-20 | |||||||||||
| Sponsor Name:Alnylam Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Multicenter, Open-label Extension Study to Evaluate the Long-term Safety and Clinical Activity of Subcutaneously Administered ALN-AS1 in Patients with Acute Intermittent Porphyria who have Comple... | |||||||||||||
| Medical condition: Acute Intermittent Porphyria (AIP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004200-21 | Sponsor Protocol Number: SUGBG-KIR-2018-001 | Start Date*: 2018-10-05 | |||||||||||
| Sponsor Name:Sahlgrenska University Hospital | |||||||||||||
| Full Title: A phase Ib/II randomized double-blind placebo controlled trial evaluating the effect of nivolumab for patients with in-transit melanoma metastases treated with isolated limb perfusion | |||||||||||||
| Medical condition: Malignant melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002893-11 | Sponsor Protocol Number: PASIPHAE | Start Date*: 2017-08-14 |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: A phase 2, international, multicenter, open-labeled, randomized trial of PAlbociclib and fulvestrant vs. Standard oral capecitabine In Patients with Hormone receptor positive/HER2 negative Advanced... | ||
| Medical condition: Hormone receptor positive/HER2 negative advanced breast cancer with endocrine resistance | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: SE (Prematurely Ended) GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002323-25 | Sponsor Protocol Number: FBCG-01-2015 | Start Date*: 2015-06-25 |
| Sponsor Name:Finnish Breast Cancer Group | ||
| Full Title: A randomized phase III study comparing trastuzumab, pertuzumab plus docetaxel (TPD) followed by 3 cycles of chemotherapy to the current standard regimen as the treatments of early HER2-positive bre... | ||
| Medical condition: Early HER-2 -positive breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: FI (Trial now transitioned) SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-004616-37 | Sponsor Protocol Number: ML29966 | Start Date*: 2016-08-03 | |||||||||||||||||||||
| Sponsor Name:GENENTECH Inc. | |||||||||||||||||||||||
| Full Title: An open-label, multicenter, biomarker study to explore the mechanism of action of ocrelizumab and B-cell biology in patients with relapsing multiple sclerosis or primary progressive multiple sclero... | |||||||||||||||||||||||
| Medical condition: Relapsing Multiple Sclerosis (RMS)/Primary Progressive Multiple Sclerosis (PPMS) | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: SE (Completed) DE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2018-002080-25 | Sponsor Protocol Number: NBG-19-01 | Start Date*: 2019-06-26 | |||||||||||
| Sponsor Name:Skåne University Hospital | |||||||||||||
| Full Title: A TRANSLATIONAL RANDOMIZED PHASE III STUDY EXPLORING THE EFFECT OF THE ADDITION OF CAPECITABINE TO CARBOPLATINUM BASED CHEMOTHERAPY IN EARLY “TRIPLE NEGATIVE” BREAST CANCER. | |||||||||||||
| Medical condition: Early triple negative breast cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000270-29 | Sponsor Protocol Number: PreVent-ACaLL | Start Date*: 2019-10-09 | |||||||||||
| Sponsor Name:Rigshopitalet/Copenhagen University Hospital | |||||||||||||
| Full Title: Short-term combined acalabrutinib and venetoclax treatment of newly diagnosed patients with CLL at high risk of infection and/or early treatment, who do not fulfil IWCLL treatment criteria for trea... | |||||||||||||
| Medical condition: Chronic Lymphocytic Leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-006227-17 | Sponsor Protocol Number: D8410C00001 | Start Date*: 2022-09-14 | |||||||||||||||||||||||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||||||||||||
| Full Title: A Modular Phase I/IIa, Open-label, Multi-centre Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of Ascending Doses of AZD9574 as Monotherapy an... | |||||||||||||||||||||||||||||||||
| Medical condition: Module 1: advanced/relapsed ovarian, breast, pancreatic or prostate cancer where patients loss of function or predicted loss of function mutation in BRCA1, BRCA2, PALB2, RAD51C, or RAD51D Mdoule 2:... | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: SE (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-001060-28 | Sponsor Protocol Number: 2020-001060-28 | Start Date*: 2021-03-16 | |||||||||||||||||||||
| Sponsor Name:Aarhus Universitet | |||||||||||||||||||||||
| Full Title: Documentation of efficacy for intralymphatic allergen immunotherapy in a phase III randomized, parallel group, double blind placebo-controlled multisite field trial | |||||||||||||||||||||||
| Medical condition: Allergic rhinitis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) SE (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2020-000664-31 | Sponsor Protocol Number: D169DC00001 | Start Date*: 2020-08-12 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: A Registry-based, Randomised, Double-blind, Placebo-Controlled Cardiovascular Outcomes Trial to Evaluate the Effect of Dapagliflozin on Cardiometabolic Outcomes in Patients without Diabetes with Ac... | ||
| Medical condition: Acute Myocardial Infarction, Heart failure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002054-39 | Sponsor Protocol Number: ODX-002 | Start Date*: 2014-11-10 | |||||||||||
| Sponsor Name:DexTech Medical AB | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled multi-centre phase II study to evaluate efficacy and tolerability of ODX (Osteodex) in Metastatic Castration Resistant Prostate Cancer (CRPC) | |||||||||||||
| Medical condition: Metastatic Castration Resistant Prostate Cancer (CRPC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-005170-19 | Sponsor Protocol Number: HP-CD-CL-2004 | Start Date*: 2018-07-30 | |||||||||||
| Sponsor Name:Renishaw Neuro Solutions Ltd. | |||||||||||||
| Full Title: A Long-Term Follow-up Safety Study for Patients with Idiopathic Parkinson’s Disease (PD) Implanted with the DDS and/or Who Received Treatment in the Main Study and/or Extension Study | |||||||||||||
| Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-000620-17 | Sponsor Protocol Number: PPL17 | Start Date*: 2019-05-08 | |||||||||||
| Sponsor Name:Dilafor AB | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Proof of Concept Study (section A) with a conditional dose finding follow up (Section B) to Evaluate the Efficacy on Cervical ripening... | |||||||||||||
| Medical condition: Induction of labor in pregnant women with unripe cervix | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001205-23 | Sponsor Protocol Number: OVERLORD-MS | Start Date*: 2020-07-10 | |||||||||||
| Sponsor Name:Helse Bergen HF, Haukeland University Hospital | |||||||||||||
| Full Title: Ocrelizumab VErsus Rituximab off-Label at the Onset of Relapsing MS Disease (OVERLORD-MS) | |||||||||||||
| Medical condition: Remitting Relapsing Multiple Sclerosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Trial now transitioned) SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001349-37 | Sponsor Protocol Number: COVID-19-HBO | Start Date*: 2020-05-08 |
| Sponsor Name:Karolinska Institutet | ||
| Full Title: A Randomized, Controlled, Open Label, Multicentre Clinical Trial to explore Safety and Efficacy of Hyperbaric Oxygen for preventing ICU admission, Morbidity and Mortality in Adult Patients With CO... | ||
| Medical condition: COVID-19 (SARS-CoV-2) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-005552-38 | Sponsor Protocol Number: ProFET | Start Date*: 2021-01-27 |
| Sponsor Name:Västragötalandsregionen, Sahlgrenska Universitetssjukhuset | ||
| Full Title: Vaginal progesterone as luteal support for improvement of live birth in frozen/thawed in-vitro fertilization natural cycles; a multicenter, open, randomized trial | ||
| Medical condition: infertility | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Trial now transitioned) IS (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003089-38 | Sponsor Protocol Number: FG001-CT-001 | Start Date*: 2020-09-03 | |||||||||||
| Sponsor Name:FluoGuide A/S | |||||||||||||
| Full Title: An open-label, dose escalation, single-dose administration, multi-center phase I/II trial of FG001 (an imaging agent), in patients with glioblastoma scheduled for neurosurgery | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004289-33 | Sponsor Protocol Number: MAAAGI | Start Date*: 2019-12-12 |
| Sponsor Name:Department of Surgical, Sciences Uppsala University | ||
| Full Title: Metformin for Abdominal Aortic Aneurysm Inhibition A randomized controlled trial MAAAGI trial | ||
| Medical condition: Small abdominal aortic aneurysm (AAA) under active surveillance; 30-49 mm in diameter for men and 30-44 mm in diameter for women | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) DK (Trial now transitioned) | ||
| 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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