- Trials with a EudraCT protocol (1,400)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,400 result(s) found for: Sterilization.
Displaying page 31 of 70.
| EudraCT Number: 2021-003209-22 | Sponsor Protocol Number: UNI50001-203 | Start Date*: 2022-02-09 | |||||||||||
| Sponsor Name:UNION therapeutics A/S | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2b Dose-Ranging Study to Evaluate the Efficacy and Safety of Orismilast in Adults with Moderate-to-Severe Plaque-Type Psoriasis | |||||||||||||
| Medical condition: Moderate-to-severe plaque-type psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-002524-12 | Sponsor Protocol Number: BNZ-20-01-2022 | Start Date*: 2023-04-13 |
| Sponsor Name:AZAD Pharma AG | ||
| Full Title: A prospective, phase III, multicenter, randomized, investigator-blinded, two-arm, parallel groups, non-inferiority clinical trial for the comparison of efficacy and safety of a preservative-free Br... | ||
| Medical condition: GLAUCOMA , OCCULAR HYPERTENSION | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BG (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-005862-30 | Sponsor Protocol Number: MHH-Pre-GvHD-001 | Start Date*: 2009-02-23 | |||||||||||
| Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
| Full Title: Pre-emptive therapy of acute graft versus host disease according to specific proteomic patterns after allogeneic hematopoietic stem cell transplantation. | |||||||||||||
| Medical condition: Pre-emptive therapy of acute graft versus host disease with prednisolone according to specific proteomic patterns after allogeneic hematopoietic stem cell transplantation. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-003205-29 | Sponsor Protocol Number: CAP2022-1 | Start Date*: 2023-02-23 | |||||||||||
| Sponsor Name:Aphaia Pharma US LLC | |||||||||||||
| Full Title: A Phase II, randomized, placebo – controlled crossover proof-of-concept study to evaluate efficacy and safety of distal jejunal-release dextrose beads formulation (APHD-012) in subjects with a path... | |||||||||||||
| Medical condition: Subjects with a pathological Oral Glucose Tolerance Test (OGTT) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004301-27 | Sponsor Protocol Number: NIBIT-M2 | Start Date*: 2012-11-08 | |||||||||||
| Sponsor Name:FONDAZIONE NIBIT | |||||||||||||
| Full Title: A randomized, Phase III study of Fotemustine versus the Combination of Fotemustine and Ipilimumab in Patients with Metastatic Melanoma with brain metastasis | |||||||||||||
| Medical condition: Subjects (men and women) 18 years old presenting with Stage IV melanoma with presence of brain metastasis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004384-39 | Sponsor Protocol Number: ABCSG-45 | Start Date*: 2018-12-18 | |||||||||||
| Sponsor Name:Austrian Breast & Colorectal Cancer Study Group (ABCSG) | |||||||||||||
| Full Title: A prospective, open, randomized, phase II study of carboplatin/olaparib in the pre-operative treatment of patients with triple-negative primary breast cancer which exhibit the features of positive ... | |||||||||||||
| Medical condition: Early invasive triple negative breast cancer with positive HRD status (acc. to Myriad mychoice© test) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001440-22 | Sponsor Protocol Number: 831 | Start Date*: 2019-07-28 |
| Sponsor Name:Skåne University Hospital | ||
| Full Title: Phase 2, multicenter, randomized, open-label, controlled, 2-arm cross-over study to evaluate the clinical efficacy and safety of a renin inhibitor, aliskiren, compared to an angiotensin converting ... | ||
| Medical condition: C3 glomerulopathy | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-006106-23 | Sponsor Protocol Number: 2020/3210 | Start Date*: 2021-07-21 | |||||||||||
| Sponsor Name:Gustave Roussy | |||||||||||||
| Full Title: Short-term Pre-OPerative Durvalumab (MEDI 4736) in early small triple negative breast cancer patients | |||||||||||||
| Medical condition: Untreated operable small triple negative breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003642-17 | Sponsor Protocol Number: OFM_DUPI_01 | Start Date*: 2018-11-23 |
| Sponsor Name:Medical University Graz | ||
| Full Title: AN EXPLORATORY STUDY TO INVESTIGATE THE BIOAVAILABILITY AND PHARMACODYNAMICS OF DUPILUMAB IN DERMAL INTERSTITIAL FLUID OF ATOPIC DER-MATITIS PATIENTS | ||
| Medical condition: Atopic Dermatitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002645-37 | Sponsor Protocol Number: KC706-C05 | Start Date*: 2006-08-25 | |||||||||||
| Sponsor Name:Kémia, Inc. | |||||||||||||
| Full Title: A Phase II randomized double-blind placebo-controlled Study of KC706 in patients with rheumatoid arthritis inadequately controlled with a stable dose of methotrexate | |||||||||||||
| Medical condition: Active rheumatoid arthritis (RA), patients taking stable doses of methotrexate | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003753-13 | Sponsor Protocol Number: P160909 | Start Date*: 2019-03-19 |
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS | ||
| Full Title: Multicentre, randomized, prospective trial comparing the efficacy and safety of Infliximab to tocilizumab in refractory or relapsing Takayasu arteritis | ||
| Medical condition: Patients with refractory or relapsing Takayasu Arteritis desease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004794-31 | Sponsor Protocol Number: KIN-1902-2001 | Start Date*: 2022-08-19 | |||||||||||
| Sponsor Name:Kinevant Sciences GmbH | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled Phase 2 Study with Open-label Extension to Assess the Efficacy and Safety of Namilumab in Subjects with Chronic Pulmonary Sarcoidosis | |||||||||||||
| Medical condition: chronic pulmonary sarcoidosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001306-30 | Sponsor Protocol Number: PROICM2021-04REL | Start Date*: 2021-09-13 | |||||||||||
| Sponsor Name:Institut Régional du Cancer de Montpellier | |||||||||||||
| Full Title: A prospective randomized phase II study to assess the schemas of retreatment with Lutathera® ([177Lu]Lu-DOTA-TATE) in patients with new progression of intestinal well-differentiated neuroendocrine ... | |||||||||||||
| Medical condition: Patients with new progression of intestinal well-differentiated neuroendocrine tumor. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-001639-10 | Sponsor Protocol Number: 787-201 | Start Date*: 2023-06-09 | |||||||||||
| Sponsor Name:Intercept Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Dose-escalation, Proof-of-Concept Study Evaluating the Safety, Tolerability, Efficacy and Pharmacokinetics of INT-787 in Subje... | |||||||||||||
| Medical condition: Severe Alcohol-Associated Hepatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004250-28 | Sponsor Protocol Number: Psoriasi_Risa | Start Date*: 2020-09-22 | |||||||||||
| Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
| Full Title: EXPLORING THE EFFECTS OF IL-23 INHIBITION BY RISANKIZUMAB ON PSORIASIS AUTOIMMUNITY. | |||||||||||||
| Medical condition: Moderate to severe psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005362-18 | Sponsor Protocol Number: HBIGforcure | Start Date*: 2022-04-13 | |||||||||||
| Sponsor Name:Hannover Medical School | |||||||||||||
| Full Title: Hepatitis B immunoglobulins to induce HBsAg clearance in patients with chronic hepatitis B | |||||||||||||
| Medical condition: HBeAg negative patients with chronic HBV infection will be allocated into two different cohorts, cohort A and cohort B. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004611-13 | Sponsor Protocol Number: G1T28-03 | Start Date*: 2017-03-16 | |||||||||||
| Sponsor Name:G1 Therapeutics | |||||||||||||
| Full Title: Phase 1b/2a Safety and Pharmacokinetic Study of G1T28 in Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer (SCLC) Receiving Topotecan Chemotherapy | |||||||||||||
| Medical condition: Extensive-Stage Small Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) BE (Completed) SI (Completed) HR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003286-34 | Sponsor Protocol Number: CHUBX2017/22 | Start Date*: 2019-03-05 | ||||||||||||||||
| Sponsor Name:CHU de Bordeaux | ||||||||||||||||||
| Full Title: In vivo involvement of the cholinergic and dopaminergic systems in the pathophysiology of apathy. | ||||||||||||||||||
| Medical condition: Apathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-001527-39 | Sponsor Protocol Number: SGN22E-002 | Start Date*: 2021-02-16 | ||||||||||||||||||||||||||
| Sponsor Name:Seagen Inc. | ||||||||||||||||||||||||||||
| Full Title: A study of enfortumab vedotin (ASG-22CE) as monotherapy or in combination with other anticancer therapies for the treatment of urothelial cancer | ||||||||||||||||||||||||||||
| Medical condition: Urothelial cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-001096-20 | Sponsor Protocol Number: UCL-mCRC-2018-MS100070-0095 | Start Date*: 2018-08-03 |
| Sponsor Name:Cliniques universitaires Saint-Luc | ||
| Full Title: Avelumab combined with cetuximab and irinotecan for treatment refractory metastatic colorectal microsatellite stable cancer – A proof of concept, open label non-randomized Phase IIa study. | ||
| Medical condition: TREATMENT FOR REFRACTORY METASTATIC MICROSATELLITE STABLE COLORECTAL CANCER | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
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