- Trials with a EudraCT protocol (2)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2 result(s) found for: Distributive shock.
Displaying page 1 of 1.
EudraCT Number: 2008-000504-92 | Sponsor Protocol Number: APX-PHP-07-008 | Start Date*: 2009-09-02 | |||||||||||
Sponsor Name:Apex Bioscience, Inc. | |||||||||||||
Full Title: PHP for the Treatment of Excess Nitric Oxide in Distributive Shock (PHOENIX) | |||||||||||||
Medical condition: Catecholamine-resistant distributive shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) BE (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005153-37 | Sponsor Protocol Number: LJ501-CRH04 | Start Date*: 2018-07-11 |
Sponsor Name:La Jolla Pharmaceutical Company | ||
Full Title: A Randomised, Placebo-controlled, Double-blind, Multicentre Efficacy and Safety Study of LJPC-501 in Paediatric Patients > 2 to 17 Years of Age with Catecholamine-Resistant Hypotension Associated w... | ||
Medical condition: Catecholamine-resistant hypotension associated with distributive shock | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) EE (Completed) LT (Prematurely Ended) FR (Completed) ES (Temporarily Halted) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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