- Trials with a EudraCT protocol (4,318)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (208)
4,318 result(s) found for: Toxicity.
Displaying page 1 of 216.
EudraCT Number: 2019-002635-28 | Sponsor Protocol Number: 69081 | Start Date*: 2019-10-14 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: The effect of hyperbaric oxygen therapy on breast cancer patients with late radiation toxicity | ||
Medical condition: Late radiation toxicity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022938-85 | Sponsor Protocol Number: AIO-LQ-0110 | Start Date*: 2011-04-27 |
Sponsor Name:AIO-Studien-gGmbH | ||
Full Title: Comparison of two preemptive treatment strategies of panitumumab mediated skin toxicity and assessment of quality of life in patients with Ras-wildtype colorectal cancer | ||
Medical condition: Panitumumab-mediated Skin toxicity in palliative treatment of Metastatic colorectal cancer with panitumumab | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004413-98 | Sponsor Protocol Number: DERMIA | Start Date*: 2018-03-27 | |||||||||||
Sponsor Name:Fundación CRIS | |||||||||||||
Full Title: “Phase II clinical trial of doxycycline 50 mg or 100 mg daily for the prevention of skin toxicity in patients with metastatic colorectal cancer treated with panitumumab and chemotherapy" | |||||||||||||
Medical condition: Cutaneous toxicity in patients with metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003617-18 | Sponsor Protocol Number: 1439A-028 | Start Date*: 2016-01-26 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: Phase IIb, Double-Blinded, Multicenter, Randomized Study to Assess the Effect on Central Nervous System (CNS) Toxicity of Switching from ATRIPLA™ (Efavirenz, Tenofovir, Emtricitabine) to MK-1439A ... | |||||||||||||
Medical condition: Human Immunodeficiency Virus-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000985-31 | Sponsor Protocol Number: RALAM-II | Start Date*: 2017-10-04 | |||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomédica | |||||||||||||
Full Title: Phase 3b, single arm, single site simplification study with dual therapy including 3TC (300 mg QD) plus Raltegravir (1200 mg QD) in virologically suppressed HIV-1 infected atients experiencing inco... | |||||||||||||
Medical condition: Virologically suppressed Human Immunodeficiency Virus-1 infected patients experiencing inconvenience, toxicity, negative impact on comorbidities or risk of drug-drug interactions with their current... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004003-12 | Sponsor Protocol Number: FluorouracilCapecitabine001 | Start Date*: 2020-01-14 |
Sponsor Name:Jessa Hospital | ||
Full Title: Implementation of pre-emptive geno- and phenotyping in 5-FU- or capecitabine-treated patients with the aim of reducing toxicity | ||
Medical condition: Gastro-intestinal cancers: stomach, pancreas, colon, rectum, anal tumors, esophagus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002258-60 | Sponsor Protocol Number: UMCN-ONCO-201302 | Start Date*: 2013-08-30 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: prediction of everolimus-induced interstitial lung disease in breast cancer patients; maximizing efficacy by reducing toxicity | |||||||||||||
Medical condition: breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001224-21 | Sponsor Protocol Number: MV18220 | Start Date*: 2005-01-14 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A 24 week, open label single arm study to evaluate the safety and efficacy of switching a toxicity causing antiretroviral (ARV) to enfuvirtide (ENF) and to assess resolution or improvement of ARV t... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003859-61 | Sponsor Protocol Number: PM0259CA232J1 | Start Date*: 2015-07-28 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Randomized Phase II study comparing single agent oral vinorelbine administered with two different schedules in patients with Advanced Non Small Cell Lung Cancer unfit for a platinum-based chemotherapy | |||||||||||||
Medical condition: Advanced Non Small Lung Cancer unfit for a platinium-based chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PL (Completed) HU (Completed) CZ (Completed) DE (Completed) AT (Completed) FR (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005116-28 | Sponsor Protocol Number: 38495 | Start Date*: 2012-09-10 |
Sponsor Name: | ||
Full Title: A phase I/II trial of Cabazitaxel +/- Rhenium-188 HEDP in patients with metastatic castration resistant prostate cancer who progressed on or after a docetaxel containing treatment. The ReCab trial | ||
Medical condition: Metastatic prostate cancer/bone metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004576-22 | Sponsor Protocol Number: IRI28 | Start Date*: 2017-07-14 |
Sponsor Name:Catharina Hospital Eindhoven | ||
Full Title: SAFETY, FEASIBILITY AND COST-ANALYSIS OF UGT1A1 GENOTYPE-GUIDED DOSING OF IRINOTECAN | ||
Medical condition: Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018878-21 | Sponsor Protocol Number: SSAT036 | Start Date*: 2010-08-16 |
Sponsor Name:St Stephen's AIDS Trust | ||
Full Title: A phase III, open-label, single centre, single-arm, pilot study to assess the feasibility of switching, individuals receiving efavirenz with continuing Central Nervous System (CNS) toxicity, to ral... | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022425-15 | Sponsor Protocol Number: MK07 | Start Date*: 2011-02-28 | |||||||||||
Sponsor Name:Universitätsklinikum Heidelberg | |||||||||||||
Full Title: ACCEPT - (ACC, Erbitux® and particle therapy) - Combined treatment of adenoid cystic carcinoma with cetuximab and IMRT plus C12 heavy ion boost (Phase I/II feasibility study) | |||||||||||||
Medical condition: Adenoid-cystic carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005540-99 | Sponsor Protocol Number: AGMT_HNO2 | Start Date*: 2013-03-05 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:AGMT – Arbeitsgemeinschaft medikamentöse Tumortherapie gemeinnützige GmbH | ||||||||||||||||||||||||||||||||||||||
Full Title: Randomised Phase II Pilot Studiy: Induction Chemotherapy with Docetaxel, Cisplatin und Cetuximab versus Docetaxel, Cisplatin und 5 FU followed by Radiotherapy with Cetuximab for locally advanced o... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Locally advanced or not resectable Carcinoma of the Head and Neck | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021382-78 | Sponsor Protocol Number: RXT-MISO-10 | Start Date*: 2011-11-14 |
Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut MAR) | ||
Full Title: Dose radiotherapy for lung cancer treatment. | ||
Medical condition: Lung cancer. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002886-20 | Sponsor Protocol Number: DHNS2013-01/MOHN01 | Start Date*: 2014-01-30 |
Sponsor Name:UMC St Radboud | ||
Full Title: A phase Ib-II study of the combination of cetuximab and methotrexate in recurrent or metastatic squamous cell carcinoma of the head and neck. A study of the Dutch Head and Neck Society. | ||
Medical condition: Recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001795-38 | Sponsor Protocol Number: ALLTogether1 | Start Date*: 2020-05-15 | |||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||
Full Title: ALLTogether1– A Treatment study protocol of the ALLTogether Consortium for children and young adults (0-45 years of age) with newly diagnosed acute lymphoblastic leukaemia (ALL) | |||||||||||||
Medical condition: Acute lymphoblastic leukaemia (ALL) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) FI (Trial now transitioned) SE (Trial now transitioned) DK (Trial now transitioned) IE (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) PT (Trial now transitioned) LT (Trial now transitioned) NO (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) IS (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005357-21 | Sponsor Protocol Number: L-9918 | Start Date*: 2006-04-24 |
Sponsor Name:ACROSS | ||
Full Title: Estudio aleatorizado fase III multicéntrico sobre la eficacia de las infusiones de calcio y magnesio en la prevención de la neurotoxicidad inducida por el tratamiento adyuvante del cáncer de colon | ||
Medical condition: COLON ADENOCARCINOMA | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001031-22 | Sponsor Protocol Number: CCR2749 | Start Date*: 2007-12-18 |
Sponsor Name:Institute of Cancer Research | ||
Full Title: The Potentiation of Efficacy of Radiotherapy in Non-Small-Cell Lung Cancer (NSCLC) by Inhibition of Akt Activation | ||
Medical condition: Non-small-cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004029-24 | Sponsor Protocol Number: TOGA 0501 | Start Date*: 2007-08-17 |
Sponsor Name:Thoracale Oncologie Groep Antwerpen TOGA | ||
Full Title: Randomized Phase II Study Evaluating The Tolerability Of Adjuvant Docetaxel-based Chemotherapy For Completely Resected Stage IB-II Non-Small Cell Lumg Cancer (NSCLC) | ||
Medical condition: Non-Small Cell Lung Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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