- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Qualitative methodology.
Displaying page 1 of 1.
| EudraCT Number: 2010-024026-38 | Sponsor Protocol Number: mex201011 | Start Date*: 2012-01-10 |
| Sponsor Name:Radboud University Nijmegen Medical Center | ||
| Full Title: Combining N-of-1 trials to estimate population clinical effectiveness of drugs using Bayesian hierarchical modeling. The case of Mexilitin for patients with Non-Dystrophic Myotonia. | ||
| Medical condition: Patients with non-dystrophic myotonic syndromes (NDMs). NDMs are caused by mutations in the gene encoding for the skeletal muscle sodium (SCN4A) or chloride (CLCN1) channel. In this study patient... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000311-98 | Sponsor Protocol Number: P2005V3 | Start Date*: 2005-11-09 |
| Sponsor Name:University of Nottingham | ||
| Full Title: A randomised controlled trial (pilot study) of the use of macerated garlic oil in patients with cystic fibrosis who have pulmonary infection with Pseudomonas aeruginosa | ||
| Medical condition: Chronic pulmonary infection with Pseudomonas aeruginosa in patients with cystic fibrosis | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-000345-12 | Sponsor Protocol Number: ABR-39476 | Start Date*: 2012-06-06 |
| Sponsor Name:VU Medical Center | ||
| Full Title: A phase II study of gefitinib and fulvestrant in patients with advanced, EGFR mutated non-small cell lung cancer pretreated with reversible EGFR tyrosine kinase inhibitors | ||
| Medical condition: Patients with pathologically documented NSCLC with an EGFR mutation, who failed previous treatment with reversible EGFR TKI’s (gefitinib or erlotinib). | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-005610-33 | Sponsor Protocol Number: IAB-CD8-203 | Start Date*: 2022-02-09 | |||||||||||
| Sponsor Name:ImaginAb, Inc. | |||||||||||||
| Full Title: iPREDICT Trial: A Phase IIB, Open Label, Study of 89Zr-Df-Crefmirlimab PET/CT in Subjects with Selected Advanced or Metastatic Malignancies including Melanoma, Merkel Cell, Renal Cell and Non-Small... | |||||||||||||
| Medical condition: To predict if patients with selected advanced or metastatic malignancies including Melanoma, Merkel Cell, Renal Cell and Non-Small Cell Lung Cancers, will respond to standard-of-care Immunotherapy ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004552-64 | Sponsor Protocol Number: 131016 | Start Date*: 2017-07-03 |
| Sponsor Name:Center for Digestive Diseases, Karolinska University Hospital | ||
| Full Title: MISTRAL - Mistletoe therapy in primary and recurrent inoperable pancreatic cancer - A phase III prospective, randomized, double blinded, multicenter, parallel group, placebo controlled clinical tr... | ||
| Medical condition: Primary or recurrent inoperable pancreatic cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-000973-69 | Sponsor Protocol Number: 0468H1-318-WW | Start Date*: 2005-04-21 |
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc | ||
| Full Title: A Randomized, Open-Label, Comparative Evaluation of the Safety and Efficacy of Sirolimus versus Cyclosporine when Combined in a Regimen Containing Basiliximab, Mycophenolate Mofetil, and Corticoste... | ||
| Medical condition: The rationale for the present study is to assess whether a CNI-free regimen including antibody induction, sirolimus, and mycophenolate mofetil (MMF) results in improved long-term renal function wit... | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) SE (Prematurely Ended) AT (Completed) GB (Completed) CZ (Prematurely Ended) ES (Completed) IT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004444-29 | Sponsor Protocol Number: RID-TB:Treat | Start Date*: 2020-11-25 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: An open-label, multi-centre, randomised controlled trial evaluating the effects of short-course rifapentine-based regimens and additional adherence support on LTBI treatment adherence and completio... | |||||||||||||
| Medical condition: Latent Tuberculosis infection (LTBI) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-005004-28 | Sponsor Protocol Number: 15SM3025 | Start Date*: 2015-12-31 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: Stratified Treatment OPtimisation for HCV-1 (STOPHCV-1) | |||||||||||||
| Medical condition: Hepatitis C Infection (HCV) (genotype 1a/1b/4) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002507-34 | Sponsor Protocol Number: GSN000200 | Start Date*: 2014-02-20 | |||||||||||||||||||||
| Sponsor Name:Genkyotex Innovation SAS | |||||||||||||||||||||||
| Full Title: A Double-Blind, Randomized, Placebo-Controlled, Phase 2 Study Evaluating the Safety and Efficacy of Oral GKT137831 in Patients with Type 2 Diabetes and Albuminuria | |||||||||||||||||||||||
| Medical condition: Patients with type 2 diabetes and albuminuria. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) PL (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
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