- Trials with a EudraCT protocol (1,640)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,640 result(s) found for: Cancer syndrome.
Displaying page 1 of 82.
EudraCT Number: 2006-001815-30 | Sponsor Protocol Number: SGUL/SGH 001 | Start Date*: 2006-06-05 | |||||||||||
Sponsor Name:St George's, University of London (SGUL) [...] | |||||||||||||
Full Title: Prevention Of Endometrial Tumours (POET) | |||||||||||||
Medical condition: Endometrial cancer/tumours in women with Hereditary Non-polyposis Colorectal Cancer (HNPCC) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000411-14 | Sponsor Protocol Number: 6639 | Start Date*: 2014-07-17 | |||||||||||
Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: A randomised double blind dose non-inferiority trial of a daily dose of 600mg versus 300mg versus 100mg of enteric coated aspirin as a cancer preventive in carriers of a germline pathological misma... | |||||||||||||
Medical condition: Lynch Syndrome also known as HNPCC (non hereditary non polyposis colorectal cancer). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FI (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003548-35 | Sponsor Protocol Number: MesaCAPP | Start Date*: 2017-03-10 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: Mesalamine for Colorectal Cancer Prevention Program in Lynch syndrome | |||||||||||||
Medical condition: Colorectal Cancer Prevention in Lynch syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) NL (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002904-11 | Sponsor Protocol Number: GOC | Start Date*: 2021-09-23 |
Sponsor Name:GERMAN ONCOLOGY CENTER | ||
Full Title: Diagnostic comparison of 18F-FDG with 18F-FAPI-74 in Thyroid Cancer patients with TENIS Syndrome | ||
Medical condition: Imaging comparison of the drug under investigation on thyroid cancer patients with TENIS syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CY (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003011-55 | Sponsor Protocol Number: MesaCAPP | Start Date*: 2020-07-23 | ||||||||||||||||
Sponsor Name:Karolinska Institute | ||||||||||||||||||
Full Title: Mesalamine for Colorectal Cancer Prevention Program in Lynch Syndrome | ||||||||||||||||||
Medical condition: Lynch Syndrome, which is increasing the risk of developing colorectal cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Trial now transitioned) DK (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020451-32 | Sponsor Protocol Number: AMCmedonc010 | Start Date*: 2010-12-10 | |||||||||||||||||||||
Sponsor Name:Academic Medical Center Amsterdam | |||||||||||||||||||||||
Full Title: Pilot study of everolimus in the treatment of advanced malignancies in patients with Peutz-Jeghers syndrome | |||||||||||||||||||||||
Medical condition: Advanced malignancy of any tumor type, not suitable for surgery at the time of study enter in patients with known Peutz-Jeghers disease (with LKB1 mutation). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004839-23 | Sponsor Protocol Number: CA-4948-102 | Start Date*: 2023-02-09 | ||||||||||||||||
Sponsor Name:Curis, Inc | ||||||||||||||||||
Full Title: A Phase 1/2a, Open-Label Dose Escalation and Cohort Expansion Study of Orally Administered CA-4948(IRAK4i) as a Monotherapy in patients with Acute Myelogenous Leukemia or Myelodysplastic Syndrome a... | ||||||||||||||||||
Medical condition: Acute Myelogenous Leukemia (AML) or high risk Myelodysplastic Syndrome (MDS). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) PL (Completed) FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004899-18 | Sponsor Protocol Number: LUSPLUS | Start Date*: 2021-09-17 | |||||||||||||||||||||
Sponsor Name:GWT-TUD GmbH | |||||||||||||||||||||||
Full Title: A phase IIIb, open-label, single arm study to evaluate the efficacy and safety of luspatercept in patients with lower-risk MDS and ring-sideroblastic phenotype (MDS-RS) | |||||||||||||||||||||||
Medical condition: Lower-risk myelodysplastic syndrome with ring-sideroblastic phenotype (MDS-RS) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002815-20 | Sponsor Protocol Number: MET07 | Start Date*: 2007-10-09 | ||||||||||||||||
Sponsor Name:Royal Surrey County Hospital | ||||||||||||||||||
Full Title: A Prospective Randomised Pilot Study of Metformin and Lifestyle Intervention in the Prevention of Metabolic Syndrome due to Androgen Deprivation Therapy in Prostate Cancer | ||||||||||||||||||
Medical condition: Patients with prostate cancer on androgen deprivation therapy (ADT). Randomisation between standard treatment with ADT only, and the additional use of metformin with dietary and exercise advice. Ai... | ||||||||||||||||||
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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: 2008-006193-15 | Sponsor Protocol Number: CL0600-020 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:NPS Pharmaceuticals, Inc. | |||||||||||||
Full Title: A 24-Week Study of the Efficacy and Safety of Teduglutide in Subjects with Parenteral Nutrition-Dependent Short Bowel Syndrome | |||||||||||||
Medical condition: Short Bowel Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) ES (Completed) FR (Completed) IT (Completed) GB (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004137-91 | Sponsor Protocol Number: Gesida92016 | Start Date*: 2018-01-23 | |||||||||||
Sponsor Name:Fundacion SEIMC-GESIDA | |||||||||||||
Full Title: A single-arm, open-label, multicenter phase IV trial to evaluate the efficacy and safety of elvitegravir / cobicistat / emtricitabine / tenofovir alfa-namide as first-line treatment in naïve patien... | |||||||||||||
Medical condition: AIDS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003810-38 | Sponsor Protocol Number: KCP-8602-801 | Start Date*: 2021-12-01 | |||||||||||||||||||||||||||||||
Sponsor Name:Karyopharm Therapeutics Inc. | |||||||||||||||||||||||||||||||||
Full Title: Phase 1/2 Open-Label Study of the Safety, Tolerability and Efficacy of the Selective Inhibitor of Nuclear Export (SINE) Compound Eltanexor (KPT-8602) in Patients with Newly Diagnosed and Relapsed/R... | |||||||||||||||||||||||||||||||||
Medical condition: High-risk primary refractory MDS patients | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014768-21 | Sponsor Protocol Number: TUD-TEMDS1-042 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Dresden Technical University | |||||||||||||
Full Title: Treatment of MDS patients with single agent temsirolimus – a pilot study | |||||||||||||
Medical condition: Myelodysplastic Syndromes (MDS) (20 IPSS LOW+INT-1 and 20 IPSS INT-2+HIGH or proliferating CMML) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006865-17 | Sponsor Protocol Number: ML20559 | Start Date*: 2007-05-24 | |||||||||||
Sponsor Name:Roche Farma, S.A. | |||||||||||||
Full Title: Estudio multicéntrico, no aleatorizado, abierto, para valorar la eficacia y la seguridad de la combinación de micofenolato mofetilo (MMF), prednisona y eritropoyetina beta en pacientes con síndrome... | |||||||||||||
Medical condition: Síndromes mielodisplásicos (SMDs) de riesgo bajo o intermedio-1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002553-29 | Sponsor Protocol Number: kk-2013 | Start Date*: 2013-08-22 | ||||||||||||||||||||||||||
Sponsor Name:Jens Sønksen | ||||||||||||||||||||||||||||
Full Title: Metabolic changes due to iatrogenic hypogonadism in patients with prostate cancer: orchiectomy vs. triptorelin | ||||||||||||||||||||||||||||
Medical condition: Men with prostate cancer where lifelong castration is indicated | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002428-36 | Sponsor Protocol Number: RG_19-271 | Start Date*: 2020-12-02 | |||||||||||||||||||||
Sponsor Name:University of Birmingham | |||||||||||||||||||||||
Full Title: A phase II trial to assess the activity of Gemtuzumab Ozogamicin Therapy in Haemophagocytic lymphohistiocytosis (HLH) or Macrophage activation syndrome (MAS) or relapsed/refractory solid tumours | |||||||||||||||||||||||
Medical condition: Haemophagocytic lymphohistiocytosis (HLH) or Macrophage activation syndrome (MAS) and relapsed/refractory solid tumours | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000679-16 | Sponsor Protocol Number: EORTC 06023 | Start Date*: 2005-05-17 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Randomized phase II trial with infliximab (Remicade) in patients with myelodysplastic syndrome and a relatively low risk of developing acute leukemia | |||||||||||||
Medical condition: myelodysplastic syndrome (MDS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005535-90 | Sponsor Protocol Number: BHS-TC-10 | Start Date*: 2013-12-09 | ||||||||||||||||
Sponsor Name:CHU Mont-Godinne | ||||||||||||||||||
Full Title: Sequential administration of 5-azacytidine (AZA) and donor lymphocyte infusion (DLI) for patients with acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS) in relapse after allogenei... | ||||||||||||||||||
Medical condition: Acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS) in relapse after allogeneic stem cell transplantation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004559-38 | Sponsor Protocol Number: RG_12-101 | Start Date*: 2012-08-08 | ||||||||||||||||
Sponsor Name:University of Birmingham | ||||||||||||||||||
Full Title: A phase 2 study of the efficacy and safety of Deferasirox administered at early iron loading in patients with transfusion-dependent Myelodysplastic Syndromes. | ||||||||||||||||||
Medical condition: Iron overload in patients being treated for Myelodysplastic syndroms (MDS) by regular blood transfusions | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002195-10 | Sponsor Protocol Number: HO89 | Start Date*: 2009-05-06 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: A Phase II randomized multicenter study to assess the efficacy of lenalidomide with or without erythropoietin and granulocyte-colony stimulating factor in patients with low and intermediate-1 risk ... | |||||||||||||
Medical condition: myelodysplastic syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: View results |
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