- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Inguinal lymph node.
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EudraCT Number: 2015-001199-23 | Sponsor Protocol Number: ICR-CTSU/2014/10048 | Start Date*: 2016-10-11 | |||||||||||
Sponsor Name:The Institute of Cancer Research | |||||||||||||
Full Title: InPACT - International Penile Advanced Cancer Trial (International Rare Cancer Initiative) | |||||||||||||
Medical condition: Locally advanced squamous carcinoma of the penis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001974-10 | Sponsor Protocol Number: CA184-029 | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Adjuvant immunotherapy with anti-CTLA-4 monoclonal antibody (ipilimumab) versus placebo after complete resection of high-risk Stage III melanoma: A randomized, doubleblind Phase 3 trial of the EORT... | |||||||||||||
Medical condition: High Risk Stage III melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) IT (Completed) SE (Completed) FI (Completed) CZ (Completed) DK (Completed) DE (Completed) ES (Completed) FR (Completed) AT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001484-27 | Sponsor Protocol Number: NL67672.091.18 | Start Date*: 2023-01-24 |
Sponsor Name:radboudumc | ||
Full Title: B cell Activation in Sjögren's Syndrome, Cutaneous Lupus Erythematodus and Systemic Sclerosis Tissues Analysis 2 | ||
Medical condition: Systemic Sclerosis Sjögren's Syndrome Cutaneous Lupus Erythematodus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000707-28 | Sponsor Protocol Number: ICR-CTSU/2008/10016 | Start Date*: 2009-03-23 | |||||||||||
Sponsor Name:The Institute of Cancer Research
[...]
1. The Institute of Cancer Research
2. University Hospitals Bristol NHS Foundation Trust |
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Full Title: A Phase II Trial of docetaxel, cisplatin and 5FU chemotherapy in locally advanced and metastatic carcinoma of the penis | |||||||||||||
Medical condition: Locally advanced and metastatic carcinoma of the penis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006059-13 | Sponsor Protocol Number: Tacho01 | Start Date*: 2012-04-16 | |||||||||||
Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
Full Title: The use of Tachosil as sealant in the prevention of lymphorrea after groin lymphadenectomy for vulvar cancer: a clinical controlled prospective trial | |||||||||||||
Medical condition: lymphedema after groin lymphadenectomy in patients with vulvar cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000514-11 | Sponsor Protocol Number: SAKK01/18 | Start Date*: 2020-04-28 | |||||||||||
Sponsor Name:Swiss Group for Clinical Cancer Research (SAKK) | |||||||||||||
Full Title: Reduced intensity radio-chemotherapy for stage IIA/B seminoma. A multicenter, open label phase II trial with two cohorts | |||||||||||||
Medical condition: stage IIA/B seminoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002692-34 | Sponsor Protocol Number: GADinLADA | Start Date*: 2020-01-08 | |||||||||||
Sponsor Name:NTNU, Dept of Clinical and Molecular Medicine, Gastrosenteret | |||||||||||||
Full Title: A pilot study on safety, feasibility and insulin-promotion by intra-inguinal lymph node injections of glutamic acid decarboxylase (GAD) in patients with LADA type of diabetes. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005441-32 | Sponsor Protocol Number: DIAGNODE-B | Start Date*: 2021-12-28 | |||||||||||
Sponsor Name:Linköping University | |||||||||||||
Full Title: DIAGNODE-B, A Phase I/II Open Label Pilot Study to evaluate the safety and feasibility of an additional intralymphatic booster administration of GAD-alum (Diamyd®) in individuals with Type 1 diabetes | |||||||||||||
Medical condition: Type 1 diabetes mellitus | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002818-40 | Sponsor Protocol Number: EHVA_T02/ANRS_VRI07 | Start Date*: 2019-10-25 | |||||||||||
Sponsor Name:Inserm-ANRS | |||||||||||||
Full Title: A Phase II randomised, placebo-controlled trial of vedolizumab with or without therapeutic HIV MVA vaccine in individuals who started antiretrovirals during primary or chronic infection | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) GB (GB - no longer in EU/EEA) ES (Ongoing) DE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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