- Trials with a EudraCT protocol (44,399)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,399 result(s) found.
Displaying page 1,814 of 2,220.
| 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: 2014-002606-20 | Sponsor Protocol Number: CV185-325/B0661037 | Start Date*: 2015-11-06 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A RANDOMIZED, OPEN-LABEL, ACTIVE CONTROLLED, SAFETY AND DESCRIPTIVE EFFICACY STUDY IN PEDIATRIC SUBJECTS REQUIRING ANTICOAGULATION FOR THE TREATMENT OF A VENOUS THROMBOEMBOLIC EVENT | |||||||||||||
| Medical condition: Venous Thromboembolism | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) Outside EU/EEA AT (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) PT (Completed) IT (Not Authorised) FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001644-10 | Sponsor Protocol Number: D5272C00002 | Start Date*: 2022-10-05 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase 2 Open-label, Long-term Extension Safety Study of Brazikumab in Participants with Moderately to Severely Active Ulcerative Colitis (EXPEDITION OLE) | |||||||||||||
| Medical condition: Ulcerative Colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Prematurely Ended) AT (Prematurely Ended) IT (Prematurely Ended) PL (Prematurely Ended) FR (Completed) HU (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000915-53 | Sponsor Protocol Number: DEXAPAE | Start Date*: 2020-10-08 | |||||||||||
| Sponsor Name:Department of Radiology, Rigshospitalet, Denmark | |||||||||||||
| Full Title: Randomized double-blind placebo-controlled trial on the efficiency of a single dose dexamethasone in reducing the postembolization syndrome in men undergoing prostatic artery embolization for benig... | |||||||||||||
| Medical condition: Benign prostatic hyperplasia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001606-29 | Sponsor Protocol Number: INCB39110-309 | Start Date*: 2019-04-03 | ||||||||||||||||||||||||||
| Sponsor Name:Incyte Corporation | ||||||||||||||||||||||||||||
| Full Title: GRAVITAS-309: A Phase 2/3 Study of Itacitinib and Corticosteroids as Initial Treatment for Chronic Graft-Versus-Host Disease | ||||||||||||||||||||||||||||
| Medical condition: Moderate or severe cGVHD | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) FR (Ongoing) SE (Completed) DE (Prematurely Ended) PL (Completed) DK (Completed) ES (Temporarily Halted) GR (Prematurely Ended) FI (Completed) IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2021-002844-66 | Sponsor Protocol Number: INCB50465-309 | Start Date*: 2022-05-30 | |||||||||||
| Sponsor Name:Incyte Corporation | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of Parsaclisib in Participants with Primary Warm Autoimmune Hemolytic Anemia (PATHWAY) | |||||||||||||
| Medical condition: Primary Warm Autoimmune Hemolytic Anemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) IT (Completed) ES (Ongoing) NL (Completed) HU (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005300-29 | Sponsor Protocol Number: SDF1 | Start Date*: 2016-06-06 |
| Sponsor Name:Malmö University, Faculty of Odontology | ||
| Full Title: Prevention and treatment of initial rotcaries among elderly in Skåne. | ||
| Medical condition: Dental caries | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004780-71 | Sponsor Protocol Number: PROFERTIL | Start Date*: Information not available in EudraCT |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: A phase III Randomized Double-Blinded Placebo-Controlled Study of Use of GnRHa during Chemotherapy for Fertility Protection of Young Women and Teenagers with Cancer - ProFertil | ||
| Medical condition: Breast Cancer Acute Leukemia Lymphomas (Hodgkin and non-Hodgkin) Sarcomas (Osteo, Soft tissue and Ewing) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-001611-50 | Sponsor Protocol Number: S67072 | Start Date*: 2022-11-15 | |||||||||||
| Sponsor Name:UZ Leuven | |||||||||||||
| Full Title: Patient reported efficacy of intranasal lysine-aspirin in controlling NSAID-exacerbated respiratory disease | |||||||||||||
| Medical condition: Aspirin-Exacerbated Respiratory Disease (AERD) in patients with Chronic Rhinosinusitis with Nasal Polyps (CRSwNP) | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003162-41 | Sponsor Protocol Number: SGZ-2018-12012 | Start Date*: 2021-02-10 | |||||||||||
| Sponsor Name:Klinikum rechts der Isar, Technische Universität München | |||||||||||||
| Full Title: An investigator-initiated, multi-center, randomized, double-blind, placebo controlled study of Dupilumab to demonstrate efficacy in subjects with nummular eczema | |||||||||||||
| Medical condition: Subjects with nummular eczema | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000355-40 | Sponsor Protocol Number: SOLARIS | Start Date*: 2021-09-20 | |||||||||||
| Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest | |||||||||||||
| Full Title: SOLARIS – A phase-II open-label study of pembrolizumab and lenvatinib in patients with advanced stage hepatocellular carcinoma who are refractory to atezolizumab and bevacizumab/ IO-based therapy | |||||||||||||
| Medical condition: advanced stage hepatocellular carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002683-31 | Sponsor Protocol Number: TUD-ALPINE-077 | Start Date*: 2021-06-24 | ||||||||||||||||
| Sponsor Name:Technische Universität Dresden | ||||||||||||||||||
| Full Title: A Phase II, single-arm trial of Atezolizumab/Platinum/Etoposide for the treatment of advanced large-cell neuroendocrine cancer of the lung | ||||||||||||||||||
| Medical condition: locally advanced or metastatic large-cell neuroendocrine carcinoma of the lung (LCNEC) not eligible for curative treatment | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-004411-11 | Sponsor Protocol Number: NeoTreme | Start Date*: 2023-05-03 | |||||||||||
| Sponsor Name: University Hospital Schleswig-Holstein, Campus Lübeck | |||||||||||||
| Full Title: Phase 2 Study of Preoperative Gemcitabine Plus Cisplatin with Durvalumab (MEDI4736) and Tremelimumab in intrahepatic cholangiocarcinoma (NeoTreme) | |||||||||||||
| Medical condition: Intrahepatic cholangiocarcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004132-22 | Sponsor Protocol Number: NPH-01 | Start Date*: 2021-01-20 | |||||||||||
| Sponsor Name:Uppsala University Hospital | |||||||||||||
| Full Title: Double-blind randomized acetazolamide trial in normal pressure hydrocephalus | |||||||||||||
| Medical condition: Normal pressure hydrocephalus | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-006674-22 | Sponsor Protocol Number: 56021927PCR2046 | Start Date*: 2022-12-12 | |||||||||||
| Sponsor Name:VÝCHODOSLOVENSKÝ ONKOLOGICKÝ ÚSTAV, a.s. | |||||||||||||
| Full Title: AD ASTRA (Androgen Deprivation with Apalutamide and STereotactic RAdiotherapy) Prospective institutional phase II study of efficacy and safety of androgen deprivation with apalutamide in high-risk ... | |||||||||||||
| Medical condition: Localized or a locally advanced high-risk prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: SK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001188-58 | Sponsor Protocol Number: IDIT001 | Start Date*: 2022-02-16 |
| Sponsor Name:Göteborgs Universitet | ||
| Full Title: The effect of anti-IL17 in new-onset type 1 diabetes: a randomized, double-blind, placebo-controlled trial | ||
| Medical condition: Type 1 diabetes | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000374-39 | Sponsor Protocol Number: ORARIALS-02 | Start Date*: 2019-07-15 | |||||||||||
| Sponsor Name:Orphazyme A/S | |||||||||||||
| Full Title: Open-label, Non-randomised Extension Trial to Assess the Long-Term Safety and Efficacy of 1200 mg/day Arimoclomol 400 mg Three Times a Day (t.i.d.) in Subjects with Amyotrophic Lateral Sclerosis (A... | |||||||||||||
| Medical condition: Amyotrophic Lateral Sclerosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) SE (Completed) BE (Completed) PL (Completed) DE (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004614-35 | Sponsor Protocol Number: ECO-02 | Start Date*: 2021-11-23 | |||||||||||
| Sponsor Name:Ismail Gögenur | |||||||||||||
| Full Title: Treatment with SGLT-2 inhibitor for postoperative hyperglycemia in acute abdominal surgery – a randomized trial | |||||||||||||
| Medical condition: Postoperative (stress) hyperglycemia in patients with no known diabetes after acute abdominal surgery | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002437-21 | Sponsor Protocol Number: GEICAM/2014-12 | Start Date*: 2015-11-09 | |||||||||||
| Sponsor Name:GEICAM (Spanish Breast Cancer Research Group Foundation) | |||||||||||||
| Full Title: A randomized, double-blind, parallel-group, multicentre, phase II study to compare the efficacy and tolerability of fulvestrant (FaslodexTM) 500mg with placebo and fulvestrant (FaslodexTM) 500mg in... | |||||||||||||
| Medical condition: Postmenopausal women presenting with HR-positive/HER2-negative metastatic breast cancer who have received at least 5 years of endocrine therapy in the adjuvant setting as treatment for early diseas... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) IE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000244-10 | Sponsor Protocol Number: EGBAB | Start Date*: 2019-12-13 |
| Sponsor Name:Region Uppsala | ||
| Full Title: Influence of antibiotic treatment on the normal flora and the presence of resistance genes in known carriers of ESBL and VRE | ||
| Medical condition: Carriage of genes coding for vancomycin resistant enterococci (VRE) and extended spectrum betalactamase producing enterobacteriales (EPE) phenotypes. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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