- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (20)
5 result(s) found for: Fexofenadine hydrochloride.
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EudraCT Number: 2017-000239-15 | Sponsor Protocol Number: SFY10717 | Start Date*: 2017-03-20 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: An open-label, uncontrolled 4-week study to assess the safety, efficacy and pharmacokinetics of Allegra® (dry syrup formulation) 15 mg or 30 mg twice daily in pediatric patients with perennial all... | |||||||||||||
Medical condition: Rhinitis perennial | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004873-34 | Sponsor Protocol Number: FFU109047 | Start Date*: 2016-12-21 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A Comparison of Fluticasone Furoate Nasal Spray (FFNS) versus Oral Fexofenadine in the Treatment of Seasonal Allergic Rhinitis | ||
Medical condition: Seasonal Allergic Rhinitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2017-000251-74 | Sponsor Protocol Number: SFY10718 | Start Date*: 2017-03-20 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: An open-label, uncontrolled 4-week study to assess the safety, efficacy and pharmacokinetics of Allegra® (dry syrup formulation) 15 mg or 30 mg twice daily in pediatric patients with atopic dermat... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001284-27 | Sponsor Protocol Number: ENHANCE | Start Date*: 2022-09-07 |
Sponsor Name:Med. Univ. Wien, Klinik f. Innere Med I, Onkologie | ||
Full Title: H1-antihistaminE treatment in combiNation with immunotHerapy in pAtieNts with advanced non small cell lung canCEr: A single- center phase II trial | ||
Medical condition: NSCLC | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004158-33 | Sponsor Protocol Number: CYP3A4/5+PGPinRenalTx | Start Date*: 2008-09-17 | |||||||||||
Sponsor Name:Department of Nephrology and Renal Transplantation, KU Leuven | |||||||||||||
Full Title: CYP3A4/5 and PGP activity in renal transplantation. A study assessing in vivo hepatic and intestinal CYP3A4/5 and PGP activity in kidney transplant recipients and its relationship with genetic and... | |||||||||||||
Medical condition: Effect of genetic (single nucleotide polymorphisms of genes encoding drug metabolising enzymes and drug transporters) and non-genetic factors (e.g. age, time after transplantation, concommitant med... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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