- Trials with a EudraCT protocol (409)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
409 result(s) found for: Menstrual cycle.
Displaying page 21 of 21.
EudraCT Number: 2009-013064-40 | Sponsor Protocol Number: HZC102970 | Start Date*: 2009-10-14 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development | |||||||||||||
Full Title: A 52-week efficacy and safety study to compare the effect of three dosage strengths of Fluticasone Furoate/GW642444 Inhalation Powder with GW642444 on the Annual Rate of Exacerbations in Subjects w... | |||||||||||||
Medical condition: Patients with Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) NL (Completed) DK (Completed) IT (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003333-42 | Sponsor Protocol Number: EZH-302 | Start Date*: 2020-11-09 | |||||||||||
Sponsor Name:Epizyme, Inc. | |||||||||||||
Full Title: A Phase 1b/3 double-blind, randomized, active-controlled, 3-stage, biomarker adaptive study of tazemetostat or placebo in combination with lenalidomide plus rituximab in subjects with relapsed/refr... | |||||||||||||
Medical condition: Relapsed/refractory follicular lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003206-25 | Sponsor Protocol Number: NRL001-01/2011(SEFI) | Start Date*: 2012-01-25 | |||||||||||
Sponsor Name:Norgine Ltd | |||||||||||||
Full Title: A multi-centre, phase II, double-blind, randomised, placebo-controlled, parallel group, dose-ranging study in patients with faecal incontinence; to evaluate the efficacy, safety and tolerability of... | |||||||||||||
Medical condition: Faecal incontinence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) DE (Completed) ES (Completed) GB (Completed) IT (Completed) HU (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2010-023419-33 | Sponsor Protocol Number: HZC112352 | Start Date*: 2011-03-17 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline S.A. | ||||||||||||||||||
Full Title: HZC112352:Estudio de 12 semanas de duración para evaluar la función pulmonar durante 24 horas de Furoato de Fluticasona /Vilanterol (FF/VI) 100/25 µg en polvo para inhalación, una vez al día, en co... | ||||||||||||||||||
Medical condition: Enfermedad Pulmonar Obstructiva Crónica (EPOC) Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) DE (Prematurely Ended) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-007107-32 | Sponsor Protocol Number: M10-301 | Start Date*: 2009-07-31 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Abbott GmbH & Co. KG | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 2 Randomized, Placebo-Controlled, Double-Blind Study of Carboplatin /Paclitaxel in Combination with ABT-869 Versus Carboplatin/Paclitaxel Alone in Subjects with Advanced or Metastatic Non-S... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Non small cell lung cancer. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: CZ (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000727-13 | Sponsor Protocol Number: MRG106-11-201 | Start Date*: 2018-12-17 | |||||||||||
Sponsor Name:miRagen Therapeutics, Inc. | |||||||||||||
Full Title: SOLAR: A Phase 2, Randomized, Open-label, Parallel-group, Active Comparator, Multi-center Study to Investigate the Efficacy and Safety of Cobomarsen (MRG-106) in Subjects with Cutaneous T-Cell Lymp... | |||||||||||||
Medical condition: Cutaneous T-Cell Lymphoma (CTCL), Mycosis Fungoides (MF) Subtype | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Completed) ES (Prematurely Ended) DE (Completed) AT (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021059-25 | Sponsor Protocol Number: HZC113107 | Start Date*: 2011-02-11 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | ||||||||||||||||||
Full Title: Estudio de 12 semanas de duración para evaluar la función pulmonar durante 24 horas de Furoato de Fluticasona (FF)/Vilanterol (VI) en polvo para inhalación (FF/VI en polvo para inhalación) una vez ... | ||||||||||||||||||
Medical condition: Enfermedad Pulmonar Obstructiva Crónica (EPOC) Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005393-32 | Sponsor Protocol Number: M13-101 | Start Date*: 2012-08-10 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: An Open-Label Study to Evaluate the Safety, Antiviral Activity and Pharmacokinetics of Direct-Acting Antiviral Agent (DAA) Treatment in Combination with Peginterferon α-2a and Ribavirin (pegIFN/RBV... | |||||||||||||
Medical condition: Chronic Hepatitis C infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) BE (Completed) HU (Completed) SE (Completed) AT (Completed) NL (Completed) IT (Completed) CZ (Prematurely Ended) IE (Completed) SK (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002219-25 | Sponsor Protocol Number: ITCA650-CLP-107 | Start Date*: 2014-09-16 | |||||||||||
Sponsor Name:Intarcia Therapeutics, Inc. | |||||||||||||
Full Title: A Randomized, Multicenter Study to Evaluate Cardiovascular Outcomes with ITCA 650 in Patients Treated with Standard of Care for Type 2 Diabetes | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) SK (Completed) EE (Completed) FI (Completed) DE (Completed) DK (Completed) ES (Completed) PL (Completed) BG (Completed) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
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