- Trials with a EudraCT protocol (843)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
843 result(s) found for: đź’Ż99.
Displaying page 1 of 43.
EudraCT Number: 2018-003242-16 | Sponsor Protocol Number: MRx-4DP0004-I-001 | Start Date*: 2019-04-09 | |||||||||||
Sponsor Name:4D pharma plc | |||||||||||||
Full Title: A first in human, double-blind, placebo-controlled, multicentre Phase I/II study to evaluate the safety, tolerability and immune modulatory effects of MRx-4DP0004, (a lyophilised formulation of Bif... | |||||||||||||
Medical condition: Asthma | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003896-41 | Sponsor Protocol Number: D5181C00001 | Start Date*: 2015-03-27 | |||||||||||
Sponsor Name:MedImmune, LLC | |||||||||||||
Full Title: A Phase 2a, Randomized, Placebo-controlled, Proof of Mechanism Study to Evaluate the Safety and Efficacy of AMG 557/MEDI5872 in Subjects with Primary Sjogren’s Syndrome | |||||||||||||
Medical condition: Primary Sjogren’s Syndrome | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002586-39 | Sponsor Protocol Number: | Start Date*: 2006-09-13 |
Sponsor Name:Radiological dept. Aalborg Hospital | ||
Full Title: Placebocontrolled trial, testing the efficacy of Polidocanol injections as a treatment of chronic achilles tendon tendinopatia | ||
Medical condition: tedinopathy of the achilles tendon | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002109-22 | Sponsor Protocol Number: 02/05/HĂĽ | Start Date*: 2005-12-01 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Comparative Effects of Telmisartan and Candesartan on glucose metabolism in patients with chronic heart failure | ||
Medical condition: both investigated drugs are well established in the treatment of heart failure or hypertension respectively. As the investigateed Patients have this conditions according to the inclusion criteria, ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000770-21 | Sponsor Protocol Number: GORTEC2019-01 | Start Date*: 2020-05-25 | |||||||||||
Sponsor Name:GORTEC | |||||||||||||
Full Title: A phase II randomized trial, non comparative, evaluating chemotherapy associated cisplatin, 5-fluorouracil and docetaxel at adapted doses in patients with locally advanced squamous cell carcinoma | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001586-87 | Sponsor Protocol Number: RSLV-132-04 | Start Date*: 2016-09-29 |
Sponsor Name:Resolve Therapeutics, LLC | ||
Full Title: A Phase 2, Double Blind, Placebo Controlled Study of RSLV-132 in Subjects with Primary Sjogren’s Syndrome | ||
Medical condition: Primary Sjogrens Syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001413-24 | Sponsor Protocol Number: 35RC15_8933_TAP-ALIF | Start Date*: 2016-06-22 | |||||||||||
Sponsor Name:CHU de Rennes | |||||||||||||
Full Title: Intérêt du TAP (Transverse Abdominis Plane) bloc bilatéral échoguidé pour l’analgésie post opératoire des chirurgies rachidiennes par voie antérieure. | |||||||||||||
Medical condition: Chirurgie du rachis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001132-19 | Sponsor Protocol Number: 1-10-72-67-17 | Start Date*: 2017-07-04 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
Full Title: Effects of Metformin on portal hypertension in patients with cirrhosis. | ||||||||||||||||||
Medical condition: cirrhosis and portal hypertension | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000573-25 | Sponsor Protocol Number: 1.1 | Start Date*: 2020-03-20 |
Sponsor Name:Aarhus University Hospital | ||
Full Title: Evaluation of patients after cardiac surgery: Novel ultrasound parameters for quantification of renal perfusion & analysis of phenylephrines’ effect on invasive haemodynamics and echocardiographic ... | ||
Medical condition: Hypotension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003771-19 | Sponsor Protocol Number: 2019-100 | Start Date*: 2019-11-19 | |||||||||||
Sponsor Name:Aarhus Universitetshospital | |||||||||||||
Full Title: The effect of improved insulin sensitivity on bone turnover markers and bone biomechanical properties in persons with type 2 diabetes mellitus | |||||||||||||
Medical condition: Type 2 diabetes mellitus Diabetic bone disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001031-72 | Sponsor Protocol Number: HP-POST-COVID | Start Date*: 2021-04-08 | |||||||||||
Sponsor Name:Aarhus University, The MR Research Center | |||||||||||||
Full Title: Metabolic MRI with hyperpolarized pyruvate in long-term COVID19 patients | |||||||||||||
Medical condition: Long-term COVID19 symptoms | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004935-26 | Sponsor Protocol Number: PIFT | Start Date*: 2021-02-25 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
Full Title: PBC induced fatigue treated with thiamine - The effect of oral thiamine supplement in 4 weeks to patients with primary biliary cholangitis (PBC) and chronic fatigue. A randomised, double-blinded, p... | ||||||||||||||||||
Medical condition: Primary biliary cholangitis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002249-40 | Sponsor Protocol Number: GNS561CLIQ0291 | Start Date*: 2020-06-30 | |||||||||||
Sponsor Name:Genoscience Pharma | |||||||||||||
Full Title: Cure COVID: A prospective, controlled, randomized study to compare the efficacy of GNS561 versus standard of care in patients with SARS-CoV-2 (COVID-19) infection. | |||||||||||||
Medical condition: COVID-19 infection | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002169-23 | Sponsor Protocol Number: DRYCHILD | Start Date*: 2017-09-06 | |||||||||||
Sponsor Name:Søren Rittig | |||||||||||||
Full Title: The effect of clinical characterization of children with monosymptomatic nocturnal enuresis on the efficacy of desmopressin and alarm therapy. | |||||||||||||
Medical condition: Enuresis nocturna | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) BE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002146-37 | Sponsor Protocol Number: INCB50465-208 | Start Date*: 2019-01-24 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 2 Dose-Escalation Study of the Safety and Tolerability of INCB050465 in Participants With Pemphigus Vulgaris | |||||||||||||
Medical condition: Pemphigus vulgaris | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002393-37 | Sponsor Protocol Number: RG_13-027 | Start Date*: 2015-01-06 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: A single arm, two-stage, multi-centre, phase II clinical trial investigating the safety and activity of the use of BTT1023, a human monoclonal antibody targeting vascular adhesion protein (VAP-1), ... | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis (PSC) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003789-15 | Sponsor Protocol Number: NMSG#20/13 | Start Date*: 2014-01-08 | |||||||||||
Sponsor Name:Nordic Myeloma Study Group | |||||||||||||
Full Title: Phase II study of carfilzomib- cyclophosphamide-dexamethasone and high-dose melphalan followed by randomization between observa-tion or maintenance with carfil-zomib and dexamethasone in pa-tients ... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) FI (Completed) SE (Completed) NO (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001030-34 | Sponsor Protocol Number: MC-0241 | Start Date*: 2019-06-12 |
Sponsor Name:Egis Pharmaceuticals PLC | ||
Full Title: A Prospective Open-label, Multicentric, Phase IV Trial to Compare the Efficacy of 10-Week Therapy of Ramipril and Indapamide SR Tablets Given Concomitantly with that of the Monotherapy of Ramipril ... | ||
Medical condition: hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000941-12 | Sponsor Protocol Number: BAY 43-9006 / 11718 | Start Date*: 2005-08-18 |
Sponsor Name:Onyx Pharmaceuticals, Inc. | ||
Full Title: Phase III randomised, placebo controlled study of sorafenib in repeated cycles of 21 days in combination with paclitaxel/carboplatin chemotherapy in subjects with unresectable stage III or stage IV... | ||
Medical condition: unresectable, advanced Stage III or Stage IV melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003302-50 | Sponsor Protocol Number: ARGX-117-2002 | Start Date*: 2022-01-31 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blinded, Placebo-Controlled, Parallel-Group, Multicenter Trial to Evaluate the Safety and Tolerability, Efficacy, Pharmacokinetics, Pharmacodynamics, and Immunogenicit... | |||||||||||||
Medical condition: Multifocal Motor Neuropathy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) DE (Completed) BE (Completed) IT (Completed) PL (Completed) AT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
