- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
18 result(s) found for: Endothelial protein C receptor.
Displaying page 1 of 1.
| EudraCT Number: 2020-002940-22 | Sponsor Protocol Number: STARDUST | Start Date*: 2021-01-13 | |||||||||||
| Sponsor Name:A.O.U. Università degli Studi della Campania "Luigi Vanvitelli" | |||||||||||||
| Full Title: EFFECTS OF THE GLP-1 RECEPTOR AGONIST LIRAGLUTIDE ON LOWER LIMB PERFUSION IN PEOPLE WITH TYPE 2 DIABETES AND PERIPHERAL ARTERY DISEASE: A RANDOMIZED CONTROLLED TRIAL | |||||||||||||
| Medical condition: Peripheral Artery Disease and type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004580-39 | Sponsor Protocol Number: TOSCA_GHDDP | Start Date*: 2018-07-18 | |||||||||||
| Sponsor Name:AOU FEDERICO II | |||||||||||||
| Full Title: Treatment of Growth Hormone Deficiency associated with Chronic Heart Failure: A Randomized, Double-Blind, Placebo-Controlled Study | |||||||||||||
| Medical condition: Growth Hormone Deficiency associated with Chronic Heart Failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003175-19 | Sponsor Protocol Number: U1111-1206-7541 | Start Date*: 2019-11-28 | |||||||||||
| Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
| Full Title: Renal effects of treatment with Empagliflozin alone or in combination with Semaglutide in patients with type 2 diabetes and albuminuria - A double blinded, randomised, placebo controlled, parallel... | |||||||||||||
| Medical condition: Type 2 diabetes with renal complications | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001172-15 | Sponsor Protocol Number: APN01-01-COVID19 | Start Date*: 2020-04-08 |
| Sponsor Name:APEIRON Biologics AG | ||
| Full Title: Recombinant human angiotensin-converting enzyme 2 (rhACE2) as a treat-ment for patients with COVID-19 | ||
| Medical condition: Severe COVID-19 POSITIVE hospitalized male or female, between 18 and ≤ 80 years of age | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) DK (Completed) AT (Completed) GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-000065-20 | Sponsor Protocol Number: LPS15919 | Start Date*: 2020-02-05 | |||||||||||
| Sponsor Name:Sanofi Aventis Groupe (SAG) | |||||||||||||
| Full Title: A randomized, open-label, active comparator, 2-arm, prospective study to assess the glycosphingolipid clearance and clinical effects of switching to agalsidase beta (Fabrazyme®) versus continuing o... | |||||||||||||
| Medical condition: Fabry disease | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: NO (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002686-19 | Sponsor Protocol Number: 2018-HJEPharma-001 | Start Date*: 2018-11-07 | |||||||||||
| Sponsor Name:Department of Cardiology, Copenhagen University Hospital Rigshospitalet | |||||||||||||
| Full Title: Interleukin-6 Receptor Antibodies for Modulating the Systemic Inflammatory Response after Out-of-Hospital Cardiac Arrest | |||||||||||||
| Medical condition: We investigate the efficacy of commercially available interleukin-6 receptor antibody 'RoActemra' for reducing the systemic inflammatory response in patients having been resuscitated after out-of-h... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-000064-21 | Sponsor Protocol Number: LPS15918 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Sanofi Aventis Groupe (SAG) | |||||||||||||
| Full Title: A randomized, open-label, active comparator, 2-arm, prospective study to assess the glycosphingolipid clearance and clinical benefits of agalsidase beta (Fabrazyme®) in male patients with classic F... | |||||||||||||
| Medical condition: Fabry's disease | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: NO (Prematurely Ended) CZ (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020426-18 | Sponsor Protocol Number: IMCLCP12-0922 | Start Date*: 2010-10-27 | |||||||||||
| Sponsor Name:ImClone LLC | |||||||||||||
| Full Title: A Randomized, Multicenter, Double-Blind, Placebo-Controlled Phase 3 Study of Weekly Paclitaxel With or Without Ramucirumab (IMC-1121B) Drug Product in Patients With Metastatic Gastric Adenocarcinom... | |||||||||||||
| Medical condition: Metastatic gastric or gastroesophageal adenocarcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) HU (Completed) RO (Completed) FR (Completed) GB (Completed) AT (Completed) LT (Completed) PT (Completed) EE (Completed) IT (Completed) BE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004418-32 | Sponsor Protocol Number: U31402-A-U202 | Start Date*: 2020-10-30 | |||||||||||
| Sponsor Name:DAIICHI SANKYO, INC | |||||||||||||
| Full Title: A MULTI-CENTER, OPEN-LABEL, PHASE 2 STUDY TO EVALUATE SAFETY AND EFFICACY OF U3-1402 IN SUBJECTS WITH ADVANCED OR METASTATIC COLORECTAL CANCER (CRC) | |||||||||||||
| Medical condition: Advanced or metastatic colorectal cancer (CRC) which is resistant, refractory, or intolerant to at least 2 prior lines of therapy, that must include all of the following agents: fluoropyrimidine, i... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001724-35 | Sponsor Protocol Number: AMASCIS-02 | Start Date*: 2020-06-16 | |||||||||||
| Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario de La Paz (FIBHULP) | |||||||||||||
| Full Title: AMASCIS-02. ALOGENIC ADIPOSE TISSUE-DERIVED MESENCHYMAL STEM CELLS IN ISCHEMIC STROKE. A PHASE IIB MULTICENTER DOUBLE BLIND PLACEBO CONTROLLED CLINICAL TRIAL. | |||||||||||||
| Medical condition: Moderate-severe ischemic stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005666-36 | Sponsor Protocol Number: IBCSG 22-00 | Start Date*: 2009-12-07 | |||||||||||
| Sponsor Name:International Breast Cancer Study Group | |||||||||||||
| Full Title: Low-dose Cytotoxics as “Anti-angiogenesis Treatment” following Adjuvant Induction Chemotherapy for Patients with ER-negative and PgR-negative Breast Cancer Maintenance Chemotherapy in Hormone Non-... | |||||||||||||
| Medical condition: Histologically proven ER-negative and PgRnegative breast cancer with either a total mastectomy with axillary clearance or a lesser procedure with axillary lymph node dissection or sentinel node pro... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004152-19 | Sponsor Protocol Number: ELASTIC2011 | Start Date*: 2012-04-18 | |||||||||||
| Sponsor Name:Ludwig Boltzmann institute for COPD and Respiratory Epidemiology | |||||||||||||
| Full Title: Effects of ROFLUMILAST on markers of subclinical atherosclerosis In stable COPD; the ELASTIC-trial | |||||||||||||
| Medical condition: chronic obstructive pulmonary disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003243-21 | Sponsor Protocol Number: XL092-303 | Start Date*: 2022-10-06 | |||||||||||
| Sponsor Name:Exelixis, Inc. | |||||||||||||
| Full Title: A Randomized Open-Label Phase 3 Study of XL092 + Atezolizumab vs Regorafenib in Subjects with Metastatic Colorectal Cancer | |||||||||||||
| Medical condition: Metastatic colorectal cancer (CRC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) FR (Trial now transitioned) BE (Trial now transitioned) PT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002563-25 | Sponsor Protocol Number: VEGF-RTX-2013 | Start Date*: 2014-01-13 | ||||||||||||||||
| Sponsor Name:VU University Medical Centre | ||||||||||||||||||
| Full Title: Pilot study to determine the effect of fractionated radiotherapy on expression of pro-angiogenic factors in oeshophagus carcinoma | ||||||||||||||||||
| Medical condition: Angiogenesis in esophageal cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-000528-39 | Sponsor Protocol Number: TAK-676-1002 | Start Date*: 2023-03-20 | |||||||||||
| Sponsor Name:Takeda Development Center Americas, Inc. (TDC Americas) | |||||||||||||
| Full Title: An Open-label, Dose Escalation, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TAK-676 as a Single Agent and in Combination With Pembrolizumab in Ad... | |||||||||||||
| Medical condition: Solid Neoplasms | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001726-13 | Sponsor Protocol Number: A4061038 | Start Date*: 2008-11-28 | ||||||||||||||||||||||||||
| Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York City, NY 10017 | ||||||||||||||||||||||||||||
| Full Title: PHASE 2 TRIAL OF AG-013736 AS FIRST-LINE TREATMENT FOR PATIENTS WITH SQUAMOUS NON-SMALL CELL LUNG CANCER RECEIVING TREATMENT WITH CISPLATIN AND GEMCITABINE | ||||||||||||||||||||||||||||
| Medical condition: Advanced non-small cell lung cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: PL (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2007-006682-33 | Sponsor Protocol Number: A4061030 | Start Date*: 2008-03-20 | ||||||||||||||||||||||||||
| Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017, USA | ||||||||||||||||||||||||||||
| Full Title: Randomzied Phase 2 Trial of AG-013736 or Bevacizumab in Combination with Paclitaxel and Carboplatin as First Line Treatment For Patients with Advanced Non-small Cell Lung Cancer | ||||||||||||||||||||||||||||
| Medical condition: First line treatment of patients with unresectable, locally advanced, recurrent or metastatic non-squamous non-small cell lung cancer (NSCLC) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) ES (Completed) CZ (Completed) FR (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-004842-92 | Sponsor Protocol Number: SECOMBIT | Start Date*: 2016-06-30 | |||||||||||
| Sponsor Name:FONDAZIONE MELANOMA ONLUS | |||||||||||||
| Full Title: A three arms prospective, randomized phase II study to evaluate the best sequential approach with combo immunotherapy (ipilimumab/nivolumab) and combo target therapy (LGX818/MEK162) in patients wit... | |||||||||||||
| Medical condition: Metastatic melanoma and BRAF mutation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) ES (Ongoing) DE (Completed) GR (Completed) AT (Prematurely Ended) GB (GB - no longer in EU/EEA) SE (Completed) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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