- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Cyclic Amp.
Displaying page 1 of 1.
EudraCT Number: 2009-010208-27 | Sponsor Protocol Number: CLCZ696B2214 | Start Date*: 2009-06-29 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A | |||||||||||||
Full Title: Estudio aleatorizado, doble ciego, multicéntrico, de grupos paralelos, controlado con tratamiento activo de doce semanas de seguimiento para evaluar la eficacia, seguridad y tolerabilidad de LCZ696... | |||||||||||||
Medical condition: Insuficiencia Cardiaca crónica | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) NL (Completed) IT (Completed) PL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002624-16 | Sponsor Protocol Number: P170907J | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANC-PUBLIQUE-HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Validation of respiratory epithelial functional assessment to predict clinical efficacy of Orkambi®. Pathway to personalized therapy in Cystic Fibrosis PREDICT-CF | |||||||||||||
Medical condition: Homozygous F508del patient aged 12 years or older | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005625-11 | Sponsor Protocol Number: DC00050/91781 | Start Date*: 2009-09-08 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: A multi-center, double-blind, double-dummy, randomized, controlled, parallel-group study to assess efficacy and safety of SH T00658ID compared to SH D593B in the treatment of primary dysmenorrhea | |||||||||||||
Medical condition: Primary dysmenorrhea in women requesting oral contraception | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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