- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Aviptadil.
Displaying page 1 of 1.
EudraCT Number: 2006-002174-22 | Sponsor Protocol Number: Avifibro | Start Date*: 2006-11-08 |
Sponsor Name:Mondobiotech Laboratories Anstalt | ||
Full Title: Influence of inhaled Aviptadil on CCL18 serum concentrations in patients with pulmonary fibrosis | ||
Medical condition: Pulmonary Fibrosis categorized as UIP or NSIP | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004219-37 | Sponsor Protocol Number: P000554 | Start Date*: 2021-03-16 | |||||||||||
Sponsor Name:Universitätsklinikum Freiburg, Leitender Ärztlicher Direktor [...] | |||||||||||||
Full Title: A randomized, prospective, multicenter, controlled and double-blinded Phase II Clinical Trial to evaluate the influence of inhaled Aviptadil on Cough and Quality of Life in Sarcoidosis patients | |||||||||||||
Medical condition: Pulmonary sarcoidosis associated with cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003621-24 | Sponsor Protocol Number: MG-101-01 | Start Date*: 2008-05-29 | ||||||||||||||||||||||||||
Sponsor Name:MondoGEN AG | ||||||||||||||||||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, dose-finding, parallel-group study to assess the hemodynamic effects, clinical efficacy, tolerability and safety of Aviptadil (Vasoactive Intestinal Pe... | ||||||||||||||||||||||||||||
Medical condition: Pulmonary arterial hypertension (PAH) due to idiopathic pulmonary arterial hypertension (IPAH), familial PAH or PAH associated with connective tissue diseases (CTD) (e.g. systemic sclerosis, system... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) BE (Completed) NL (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) DE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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