- Trials with a EudraCT protocol (40)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
40 result(s) found for: Precursors.
Displaying page 1 of 2.
EudraCT Number: 2014-002756-11 | Sponsor Protocol Number: 43739 | Start Date*: 2014-08-27 | |||||||||||
Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
Full Title: Photodynamic therapy with varying application times for treatment of actinic keratosis | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003003-29 | Sponsor Protocol Number: 49301 | Start Date*: 2015-08-31 | |||||||||||
Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
Full Title: 5-flourouracil treatment prior to photodynamic therapy of actinic keratosis on the hands | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004681-15 | Sponsor Protocol Number: KIMCL_TS_2011-09 | Start Date*: 2011-11-09 |
Sponsor Name:Medizinische Universität Graz | ||
Full Title: Effects of the activation of peroxisome proliferator-activated receptors in patients with primary biliary cirrhosis | ||
Medical condition: Up to 67% of PBC patients have an incomplete biochemical response to UDCA and remain at increased risk for progression to cirrhosis and liver-related death. In this study we will prospectively exam... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-003944-23 | Sponsor Protocol Number: UFK-HEF 5 | Start Date*: 2005-04-20 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Acetyl salicylic acid in the treatment of patients with positive margins after surgery for cervical dysplasia grade II-III: A phase II trial | ||
Medical condition: Cervical intraepithelial neoplasia grade II/III with positive margin after surgery | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-005761-23 | Sponsor Protocol Number: CTD-TCNPC-201 | Start Date*: 2016-09-26 | |||||||||||
Sponsor Name:Cyclo Therapeutics, Inc. | |||||||||||||
Full Title: A Phase I/II study to evaluate the safety and pharmacokinetics of intravenous Trappsol Cyclo (HP-β-CD) in patients with Niemann-Pick disease type C (NPC-1) and the pharmacodynamic effects of treatm... | |||||||||||||
Medical condition: Niemann-Pick disease type C | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Completed) IT (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005199-17 | Sponsor Protocol Number: IIBSP-TIM-2013-156 | Start Date*: 2014-07-16 |
Sponsor Name:Institut de Recerca HSCSP | ||
Full Title: Efficacy and safety of topical administration of timolol maleate 0.5% solution in the treatment of Child Proliferative Hemangioma Early Stage Surface. Randomized Controlled Study | ||
Medical condition: Children Superficial Hemangioma | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-000161-40 | Sponsor Protocol Number: AdrenalClock | Start Date*: 2022-07-18 |
Sponsor Name:Medical University of Vienna, Division of Endocrinology | ||
Full Title: Investigating cardiometabolic risk factors and changes in chronobiology patterns in patients with autonomous adrenal cortisol secretion | ||
Medical condition: Autonomous cortisol secretion in patients with adrenal adenoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005438-39 | Sponsor Protocol Number: 40736 | Start Date*: 2014-04-01 | |||||||||||
Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
Full Title: Pulse photodynamic therapy with methyl aminolevulinate activated by a halogen lamp | |||||||||||||
Medical condition: Actinic keratoses | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000945-29 | Sponsor Protocol Number: ASSTBS-ONCO-ABACUS-16 | Start Date*: 2016-06-16 | |||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: Activity of Abiraterone Acetate in the management of Cushing’s syndrome in patients with adrenocortical carcinoma (ABACUS) | |||||||||||||
Medical condition: Cushing’s syndrome in patients with adrenocortical carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001796-37 | Sponsor Protocol Number: ALENDRONATO | Start Date*: 2006-06-07 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
Full Title: Effect of alendronate on spontaneous osteoclastogenesis in postmenopausal osteoporosis | |||||||||||||
Medical condition: postmenopausal osteoporosis | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001701-33 | Sponsor Protocol Number: 58161 | Start Date*: 2017-05-19 | |||||||||||
Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
Full Title: Photodynamic therapy without curettage | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000376-41 | Sponsor Protocol Number: VORIGENIPHARM | Start Date*: 2019-06-18 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Fundación de Investigación del Hospital Universitario La Paz (FIBHULP) | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Randomized and multicenter clinical trial to evaluate the effectiveness and efficiency of a voriconazole preemptive genotyping strategy in patients with risk of aspergillosis. | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Invasive fungal disease in the hematologic patient. | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001166-13 | Sponsor Protocol Number: COU-AA-001 | Start Date*: 2005-09-21 | |||||||||||
Sponsor Name:Cougar Biotechnology, Inc | |||||||||||||
Full Title: A Phase I/II Open Label Study of the 17α-hydroxylase/ C17,20 lyase inhibitor, Abiraterone acetate, in Patients with Prostate Cancer who have failed hormone therapy | |||||||||||||
Medical condition: Hormone refractory prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006156-36 | Sponsor Protocol Number: EZEHIV06 | Start Date*: 2007-04-27 | |||||||||||
Sponsor Name:Hospital Clinic, Barcelona | |||||||||||||
Full Title: Papel de los niveles plasmáticos de fitosterol en la predicción del efecto hipolipemiante de la ezetimiba en sujetos infectados por VIH que reciben inhibidores de la proteasa. ROLE OF PHYTOSTEROL ... | |||||||||||||
Medical condition: Infección crónica por VIH Hipercolesterolemia Chronic HIV infection hypercholesterolemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005084-14 | Sponsor Protocol Number: 56297 | Start Date*: 2017-01-23 | |||||||||||
Sponsor Name:Deoartment of Dermatology D92, Bispbjerg Hospital | |||||||||||||
Full Title: PpIX in curetted and non-curetted skin after Metvix application | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001151-22 | Sponsor Protocol Number: Alesaa | Start Date*: 2007-06-06 | ||||||||||||||||||||||||||
Sponsor Name:UNIVERSITA` DEGLI STUDI DI NAPOLI FEDERICO II | ||||||||||||||||||||||||||||
Full Title: ALEMTUZUMAB AND LOW-DOSE CYCLOSPORINE-A AS ALTERNATIVE IMMUNOSUPPRESSIVE TREATMENT FOR SEVERE APLASTIC ANEMIA (SAA) AND SINGLE-LINEAGE APLASTIC PATIENTS. | ||||||||||||||||||||||||||||
Medical condition: Aplastic anemia and single-lineage bone marrow failure | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001169-34 | Sponsor Protocol Number: HPV_Elimination | Start Date*: 2021-03-24 | ||||||||||||||||
Sponsor Name:Region Stockholm [...] | ||||||||||||||||||
Full Title: Concomitant HPV vaccination and HPV screening for rapid elimination of HPV infection and cervical cancer in Sweden | ||||||||||||||||||
Medical condition: HPV infection and related diseases, such as cervical intraepithelial neoplasia grade 2 and 3 and cervical cancer. | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003760-30 | Sponsor Protocol Number: EMR63325-021 | Start Date*: 2014-04-30 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled phase III trial of tecemotide versus placebo in subjects with completed concurrent chemo-radiotherapy for unresectable stage III non-smal... | |||||||||||||
Medical condition: unresectable stage III non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) AT (Completed) BE (Completed) DE (Prematurely Ended) SE (Completed) PT (Completed) IT (Completed) IE (Completed) SK (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-018092-14 | Sponsor Protocol Number: CRAD001RDE35T | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Krankenhaus Nordwest GmbH | ||||||||||||||||||
Full Title: A randomized, double-blind, multi-center phase III study evaluating paclitaxel with and without RAD001 in patients with gastric carcinoma who have progressed after therapy with a fluoropyrimidine/p... | ||||||||||||||||||
Medical condition: advanced (i.e. inoperable, recurrent or metastatic) gastric cancer or adenocarcinoma of the esophagogastric junction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001280-13 | Sponsor Protocol Number: A536-05 | Start Date*: 2014-09-03 | ||||||||||||||||
Sponsor Name:Acceleron Pharma Inc. | ||||||||||||||||||
Full Title: An Open-Label Extension Study to Evaluate the Long-Term Effects of ACE-536 for the Treatment of Anemia in Patients with Low or Intermediate-1 Risk Myelodysplastic Syndromes (MDS) Previously Enrolle... | ||||||||||||||||||
Medical condition: Myelodysplastic Syndromes (MDS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
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