- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Cardiovascular syphilis.
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EudraCT Number: 2016-003575-21 | Sponsor Protocol Number: | Start Date*: 2017-07-25 | |||||||||||
Sponsor Name:MRC Clinical Trials Unit at UCL | |||||||||||||
Full Title: A multicentre, 48 week randomised controlled factorial trial of adding maraviroc and/or metformin for hepatic steatosis in HIV-1-infected adults on combination antiretroviral therapy. | |||||||||||||
Medical condition: Hepatic steatosis in adults with chronic HIV-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003166-39 | Sponsor Protocol Number: ChImDLP-2 | Start Date*: 2022-08-08 | |||||||||||
Sponsor Name:UAB Froceth | |||||||||||||
Full Title: A study of the safety of chemoimmunotherapy with autologous Dendritic Cell Preparations in patients with stage III ovarian cancer | |||||||||||||
Medical condition: Stage III of high malignancy Ovarian serous adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002302-39 | Sponsor Protocol Number: RSV-M-301 | Start Date*: 2016-09-06 | |||||||||||
Sponsor Name:Novavax, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Observer-Blind, Placebo-Controlled, Group-Sequential Study to Determine the Immunogenicity and Safety of a Respiratory Syncytial Virus (RSV) F Nanoparticle Vaccine with Alumi... | |||||||||||||
Medical condition: Respiratory syncytial virus (RSV) is the leading viral cause of severe lower respiratory tract disease in infants and young children worldwide. In industrialized countries, nearly all children have... | |||||||||||||
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Population Age: In utero, Newborns, Infants and toddlers, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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