- Trials with a EudraCT protocol (44,364)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,364 result(s) found.
Displaying page 1,933 of 2,219.
| EudraCT Number: 2018-001158-82 | Sponsor Protocol Number: GESIDA10418 | Start Date*: 2018-09-21 | |||||||||||
| Sponsor Name:Fundación SEIMC-GESIDA | |||||||||||||
| Full Title: Phase IV, Open Label, Randomized, Clinical Trial to Evaluate the Reversibility of abacavir/lamivudine/dolutegravir CNS-Related Neurotoxicity After Switching to tenofovir alafenamide/emtricitabine/d... | |||||||||||||
| Medical condition: HIV | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003438-12 | Sponsor Protocol Number: KALIPO | Start Date*: 2008-08-29 | |||||||||||
| Sponsor Name:Fundación SEIMC-GESIDA | |||||||||||||
| Full Title: Ensayo Clínico aleatorizado para comparar la combinación ZDV + 3TC + ABC (Trizivir) frente a Lopinavir/R (Kaletra) en monoterapia en pacientes con supresión viral en tratamiento previo con ZDV + 3T... | |||||||||||||
| Medical condition: Pacientes infectados por VIH-1 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005247-78 | Sponsor Protocol Number: OB003 | Start Date*: 2022-01-19 | |||||||||||
| Sponsor Name:Oxygen Biotech s.r.o. | |||||||||||||
| Full Title: A 2-Part, Open-label, Non-randomized (Part A) and Randomized, Double-blinded, Placebo-controlled (Part B) multicentric, international study with adaptive design to evaluate safety and tolerability ... | |||||||||||||
| Medical condition: COVID-19 patients suffering from moderate to severe pneumonia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003466-13 | Sponsor Protocol Number: GMALL082013 | Start Date*: 2015-09-15 | ||||||||||||||||
| Sponsor Name:Goethe University Frankfurt | ||||||||||||||||||
| Full Title: Treatment optimization in adult patients with newly diagnosed acute lymphoblastic leukemia or lymphoblastic lymphoma by individualised, targeted and intensified treatment - a phase IV-trial with a ... | ||||||||||||||||||
| Medical condition: Newly diagnosed acute lymphoblastic leukemia or lymphoblastic lymphoma Age 18 to 55 y | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-004196-40 | Sponsor Protocol Number: GMRx2-HTN-2020-ACT1 | Start Date*: 2021-03-22 | |||||||||||
| Sponsor Name:George Medicines Pty Ltd | |||||||||||||
| Full Title: Efficacy and safety of GMRx2 (a single pill combination containing telmisartan/amlodipine/indapamide) compared to dual combinations for the treatment of hypertension: An international, multi-center... | |||||||||||||
| Medical condition: Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004939-73 | Sponsor Protocol Number: LINACLOTIDEPLACEBO | Start Date*: 2014-05-13 |
| Sponsor Name:KULEUVEN | ||
| Full Title: A RANDOMISED, PLACEBO-CONTROLLED, CROSSOVER STUDY TO EVALUATE THE EFFECT OF LINACLOTIDE ON COLONIC MOTILITY ASSESSED WITH INTRALUMINAL COLONIC MANOMETRY IN HEALTHY SUBJECTS | ||
| Medical condition: COLONIC MOTILITY WILL BE STUDIED IN HEALTHY SUBJECTS | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-000641-13 | Sponsor Protocol Number: BIO89-100-221 | Start Date*: 2020-09-30 | |||||||||||
| Sponsor Name:89bio, Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Explore the Efficacy and Safety of BIO89-100 in Subjects with Severe Hypertriglyceridemia | |||||||||||||
| Medical condition: Severe Hypertriglyceridemia (SHTG) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000459-41 | Sponsor Protocol Number: PSMA-617-01 | Start Date*: 2018-09-04 | |||||||||||
| Sponsor Name:Endocyte, Inc., A Novartis Company | |||||||||||||
| Full Title: VISION: An international, prospective, open label, multicenter, randomized Phase 3 study of 177LU-PSMA-617 in the treatment of patients with progressive PSMA-positive metastatic castration-resistan... | |||||||||||||
| Medical condition: PSMA-positive metastatic castration-resistant prostate cancer (mCRPC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) SE (Completed) FR (Completed) DK (Completed) NL (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002423-19 | Sponsor Protocol Number: BGB-A317-301 | Start Date*: 2018-08-24 | |||||||||||
| Sponsor Name:BeiGene, Ltd. | |||||||||||||
| Full Title: A Randomized, Open-label, Multicenter Phase 3 Study to Compare the Efficacy and Safety of BGB-A317 versus Sorafenib as First-Line Treatment in Patients with Unresectable Hepatocellular Carcinoma | |||||||||||||
| Medical condition: Unresectable Hepatocellular Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) CZ (Completed) FR (Completed) ES (Ongoing) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005007-12 | Sponsor Protocol Number: 039(C)MD21046 | Start Date*: 2023-02-17 | |||||||||||
| Sponsor Name:Angelini Pharma S.p.A. | |||||||||||||
| Full Title: Efficacy of Trazodone Once-a-Day for treatment of Major Depressive Disorder in patients with breast cancer. | |||||||||||||
| Medical condition: Major Depressive Disorder | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001954-76 | Sponsor Protocol Number: TV48531-CV-40190 | Start Date*: 2022-02-23 | |||||||||||
| Sponsor Name:Ratiopharm GmbH Teva EU Medical Affairs | |||||||||||||
| Full Title: A Randomized Open Label, Parallel Group Study to Evaluate the Hemodynamic Effects of Cafedrine/Theodrenaline vs Norepinephrine in the Treatment of Intraoperative Arterial Hypotension in Adults afte... | |||||||||||||
| Medical condition: The purpose of the study is to comparatively evaluate the hemodynamic effects of two treatments when intraoperative hypotension occurs. Patients who require advanced hemodynamic monitoring and dev... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003536-92 | Sponsor Protocol Number: CY6031 | Start Date*: 2022-05-09 | |||||||||||
| Sponsor Name:Cytokinetics, Inc. | |||||||||||||
| Full Title: A Phase 3, Multi-Center, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy and Safety of CK-3773274 in Adults with Symptomatic Hypertrophic Cardiomyopathy and Left Ventric... | |||||||||||||
| Medical condition: obstructive hypertrophic cardiomyopathy (oHCM) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DK (Completed) ES (Ongoing) NL (Completed) CZ (Completed) PL (Completed) PT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000090-15 | Sponsor Protocol Number: 213749 | Start Date*: 2022-12-19 | |||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals SA | |||||||||||||
| Full Title: A Phase 1/2 randomized, observer-blinded, multi-country study to evaluate safety and immunogenicity of investigational adjuvanted human papillomavirus vaccine in females (16 to 26 years of age) | |||||||||||||
| Medical condition: Active immunisation for the prevention of human papillomavirus infection | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) LT (Completed) FR (Completed) BG (Completed) EE (Completed) CZ (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001906-61 | Sponsor Protocol Number: 20180115 | Start Date*: 2020-05-18 | |||||||||||
| Sponsor Name:Amgen Inc. | |||||||||||||
| Full Title: Phase 2 Study of Talimogene Laherparepvec in Combination With Pembrolizumab in Subjects With Unresectable/Metastatic Stage IIIB-IVM1d Melanoma Who Have Progressed on Prior Anti PD-1 Based Therapy | |||||||||||||
| Medical condition: Unresectable/Metastatic Stage IIIB-IVM1d Melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) GR (Completed) PL (Prematurely Ended) ES (Ongoing) FR (Prematurely Ended) GB (GB - no longer in EU/EEA) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-000996-17 | Sponsor Protocol Number: 2 | Start Date*: 2019-05-16 |
| Sponsor Name:Thomas Møller Jensen | ||
| Full Title: Risk of post-polypectomy bleeding in patients on uninterrupted Clopidogrel therapy before polypectomy of sessile polyps; a double-blinded randomised controlled trial | ||
| Medical condition: Post polypectomy bleeding | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-001302-25 | Sponsor Protocol Number: 2008-0312-08 | Start Date*: 2009-11-05 | |||||||||||
| Sponsor Name:Lab for pharmaceutical biology [...] | |||||||||||||
| Full Title: Evaluation of the benefits and effects of hypericin Photodynamic therapy (PDT) in the clinical treatment of superficial bladder carcinoma. | |||||||||||||
| Medical condition: the study population consists of 10 patients with anatomopathologically proven muscle invasive TCC without metastasis. These patients require a cystoscopy. Before the planned cystoscopy, the bladde... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003668-11 | Sponsor Protocol Number: E7080-G000-604 | Start Date*: 2018-07-30 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Eisai Ltd. | ||||||||||||||||||||||||||||||||||||||
| Full Title: An open-label, multi-center, roll-over study to assess long term safety of lenvatinib monotherapy or lenvatinib combination regimen or comparator treatment arm to cancer patients in Eisai sponsored... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: solid tumors or lymphomas, as defined in parent protocol | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) NL (Completed) ES (Prematurely Ended) BE (Completed) IT (Completed) RO (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2013-000319-26 | Sponsor Protocol Number: CLDK378A2301 | Start Date*: 2013-08-14 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A phase III multicenter, randomized study of oral LDK378 versus standard chemotherapy in previously untreated adult patients with ALK rearranged (ALK-positive), stage IIIB or IV, non-squamous non-s... | |||||||||||||
| Medical condition: Non-small cell lung cancer (NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) AT (Prematurely Ended) IT (Completed) NL (Prematurely Ended) DE (Completed) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) FR (Prematurely Ended) GR (Completed) HU (Completed) IE (Prematurely Ended) PL (Prematurely Ended) DK (Completed) NO (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002249-13 | Sponsor Protocol Number: 3125001 | Start Date*: 2019-02-04 | ||||||||||||||||
| Sponsor Name:Orion Corporation Orion Pharma | ||||||||||||||||||
| Full Title: SAFETY AND PHARMACOKINETICS OF ODM-209 IN PATIENTS WITH METASTATIC CASTRATION-RESISTANT PROSTATE CANCER OR ESTROGEN RECEPTOR-POSITIVE, HUMAN EPIDERMAL GROWTH FACTOR RECEPTOR 2-NEGATIVE ADVANCED BRE... | ||||||||||||||||||
| Medical condition: METASTATIC CASTRATION-RESISTANT PROSTATE CANCER OR ESTROGEN RECEPTOR-POSITIVE, HUMAN EPIDERMAL GROWTH FACTOR RECEPTOR 2-NEGATIVE ADVANCED BREAST CANCER | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FI (Completed) DK (Completed) ES (Prematurely Ended) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2022-001377-31 | Sponsor Protocol Number: HZNP-DAX-203 | Start Date*: 2022-12-09 | |||||||||||
| Sponsor Name:Horizon Therapeutics Ireland DAC | |||||||||||||
| Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PHASE 2 STUDY EVALUATING THE EFFICACY AND SAFETY OF DAXDILIMAB IN ADULT PARTICIPANTS WITH ACTIVE PROLIFERATIVE LUPUS NEPHRITIS | |||||||||||||
| Medical condition: ACTIVE PROLIFERATIVE LUPUS NEPHRITIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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