- Trials with a EudraCT protocol (392)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
392 result(s) found for: Curative care.
Displaying page 1 of 20.
EudraCT Number: 2021-000872-13 | Sponsor Protocol Number: 202000865 | Start Date*: 2021-03-02 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Vaccination against cOvid In CancEr | ||
Medical condition: solid tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
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: 2009-011299-32 | Sponsor Protocol Number: 20060359 | Start Date*: 2010-08-06 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center Phase 3 Study of Denosumab as Adjuvant Treatment for Women with Early-Stage Breast Cancer at High Risk of Recurrence | |||||||||||||
Medical condition: Early-stage non-metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PT (Completed) HU (Completed) GB (Completed) ES (Prematurely Ended) CZ (Completed) LV (Completed) FR (Completed) BE (Completed) SK (Completed) NL (Completed) IE (Prematurely Ended) DK (Completed) SI (Completed) GR (Completed) IT (Completed) BG (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000080-85 | Sponsor Protocol Number: 17-245 | Start Date*: 2018-11-29 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Pilot study of the pharmacokinetic profile of paracetamol subcutaneously versus intravenously in patients receiving palliative care | |||||||||||||
Medical condition: Major patients in palliative care | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001087-36 | Sponsor Protocol Number: Bay43-9006/12414 | Start Date*: 2008-08-18 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: A Phase III randomized, double-blind, placebo-controlled study of sorafenib as adjuvant treatment for hepatocellular carcinoma after surgical resection or local ablation. | |||||||||||||
Medical condition: To evaluate the clinical benefit of sorafenib vs placebo as adjuvant treatment in subjects with HCC who received potentially curative treatment (surgical resection or local ablation). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) ES (Completed) AT (Completed) BE (Completed) FR (Completed) IT (Completed) PT (Completed) DE (Completed) GR (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001676-29 | Sponsor Protocol Number: MK3475_PROMO | Start Date*: 2016-10-27 |
Sponsor Name:Oslo University Hospital (OUS) | ||
Full Title: PROMO: A phase II study of Pembrolizumab in patients with Relapsed Or Metastatic Osteosarcoma not eligible for curative surgery | ||
Medical condition: Osteosarcoma, not eligible for curative surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004154-41 | Sponsor Protocol Number: ISO-CC-007 | Start Date*: 2018-11-07 | |||||||||||
Sponsor Name:Isofol Medical AB | |||||||||||||
Full Title: A randomized, multicenter, parallel-group, Phase III study to compare the efficacy of arfolitixorin versus leucovorin in combination with 5 fluorouracil, oxaliplatin, and bevacizumab in patients wi... | |||||||||||||
Medical condition: First line advanced Colorectal patients eligible for treatment with 5-FU, oxaliplatin, and bevacizumab. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) DE (Prematurely Ended) FR (Prematurely Ended) AT (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003596-35 | Sponsor Protocol Number: MEK116540 | Start Date*: 2015-12-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An Open-Label, Dose-Escalation, Phase I/II Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of the MEK Inhibitor Trametinib in Children and Adolescents Subj... | |||||||||||||
Medical condition: Children and Adolescents with Cancers Harboring V600 mutations | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005748-12 | Sponsor Protocol Number: 2012.761 | Start Date*: 2013-04-26 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: D2 Resection and HIPEC (Hyperthermic intraperitoneal chemoperfusion) in locally advanced gastric carcinoma. A national randomized and multicentric phase III study | |||||||||||||
Medical condition: Gastric adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003498-16 | Sponsor Protocol Number: LOXO-TRK-15003 | Start Date*: 2017-02-10 | ||||||||||||||||||||||||||
Sponsor Name:Loxo Oncology Inc. | ||||||||||||||||||||||||||||
Full Title: A Phase 1/2 Study of the Oral TRK Inhibitor LOXO-101 in Pediatric Patients with Advanced Solid or Primary Central Nervous System Tumors | ||||||||||||||||||||||||||||
Medical condition: Central Nervous System Neoplasms and advanced solid tumors | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) SE (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) IE (Trial now transitioned) PL (Completed) IT (Trial now transitioned) CZ (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000842-32 | Sponsor Protocol Number: GS-US-540-5774 | Start Date*: 2020-03-18 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants with Moderate COVID-19 Compared to Standard of Care Treatment | |||||||||||||
Medical condition: Coronavirus disease 2019 (COVID-19) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (Completed) IT (Completed) NL (Completed) GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001938-42 | Sponsor Protocol Number: UCL-ONCO2011-01 | Start Date*: 2012-01-24 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: Randomized Phase II Study of CABAZITAXEL versus METHOTREXATE in patients with recurrent or metastatic squamous cell carcinoma of the head and neck previously treated with platinum-based therapy | ||
Medical condition: To evaluate the efficacy of cabazitaxel in patients with palliative head and neck previously treated with platinum-based therapy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000393-76 | Sponsor Protocol Number: ZKI-SCT-HAPLO-0106 | Start Date*: 2006-10-25 |
Sponsor Name:Johann Wolfgang Goethe-Universität Frankfurt am Main | ||
Full Title: Allogenic stem cell transplantation with CD3/CD19 depleted stem cells from haploidentical related and non-related donators in pediatric patients with and without malignant systemic diseases. | ||
Medical condition: Pediatric patients with malignant and non-malignant high-risk diseases, where the allogeneic stem cell transplantation represents the only option for a curative therapy and where an adequate HLA-id... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-000135-40 | Sponsor Protocol Number: 260585 | Start Date*: 2016-05-12 | ||||||||||||||||||||||||||
Sponsor Name:Zealand University Hospital, Department of Surgery | ||||||||||||||||||||||||||||
Full Title: Endoscopic assisted electrochemotherapy in addition to neoadjuvant treatment of locally advanced rectal cancer: a randomized clinical phase II trial. | ||||||||||||||||||||||||||||
Medical condition: Locally advanced rectal cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003925-42 | Sponsor Protocol Number: ESR-19-14451 | Start Date*: 2021-10-14 | |||||||||||
Sponsor Name:Clinics of Munich University LMU | |||||||||||||
Full Title: A randomized open-label phase II study on the effect of durvalumab and tremelimumab combined with personalized SIRT (p-SIRT), standard-dose SIRT (sd-SIRT) or immunotherapy followed by on-demand loc... | |||||||||||||
Medical condition: Patients with hepatocellular cancer, not amenable to curative surgical or ablation 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: 2020-000835-33 | Sponsor Protocol Number: 300513 | Start Date*: 2020-04-15 | |||||||||||
Sponsor Name:Zealand University Hospital | |||||||||||||
Full Title: Neoadjuvant electrochemotherapy for colorectal cancer – a randomized controlled trial | |||||||||||||
Medical condition: Colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003141-25 | Sponsor Protocol Number: 1643/2015 | Start Date*: 2015-10-06 |
Sponsor Name:Medical University Vienna, Department of Anesthesia, Intensive Care Medicine and Pain Management | ||
Full Title: Determination of the minimal alveolar concentrations of sevoflurane in patients with end stage kidney disease | ||
Medical condition: Renal transplantation is the curative treatment in patients with end stage kidney disease. These patients have altered intraoperative anesthetic requirements compared with patients with maintained ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-003676-39 | Sponsor Protocol Number: 109147 | Start Date*: 2021-07-20 |
Sponsor Name: | ||
Full Title: Effects of sodium lactate infusion in patients with glucose transporter 1 deficiency syndrome (GLUT1DS) | ||
Medical condition: In glucose transporter 1 deficiency syndrome (GLUT1DS) cerebral glucose uptake from the systemic blood circulation is limited, because of deficient transport of glucose across the blood-brain barri... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002478-29 | Sponsor Protocol Number: CA224-063 | Start Date*: 2019-11-27 | |||||||||||
Sponsor Name:University Hospital Essen | |||||||||||||
Full Title: Neoadjuvant nivolumab combination treatment in resectable non-small cell lung cancer patients: Defining optimal combinations and determinants of immunological response (NEOpredict-Lung) | |||||||||||||
Medical condition: non-small cell lung cancer (NSCLC) of clinical stages IB, II and selected stage III A | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000189-45 | Sponsor Protocol Number: | Start Date*: 2018-03-26 |
Sponsor Name:University of Padova | ||
Full Title: Adjuvant treatment for high-risk triple negative breast cancer patients with the anti-pd-l1 antibody Avelumab: A phase III randomized trial | ||
Medical condition: High risk triple negative (ER negative, PR negative, HER2 negative) breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) IT (Trial now transitioned) | ||
Trial results: (No results available) |
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