- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
5 result(s) found for: Methane.
Displaying page 1 of 1.
EudraCT Number: 2019-002856-18 | Sponsor Protocol Number: Mannitol_03-2018 | Start Date*: 2020-06-04 | |||||||||||
Sponsor Name:NTC s.r.l. | |||||||||||||
Full Title: Efficacy and Safety of mAnniTol in bowel preparation: assessment of adequacy and presence of Intestinal levelS of hydrogen and methane during elective colonoscopy aFter mAnnitol or standard split 2... | |||||||||||||
Medical condition: Subjects scheduled for elective colonoscopy to be prepared and performed according to ESGE (European Society of Gastrointestinal Endoscopy - ESGE) guidelines. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018091-34 | Sponsor Protocol Number: CICL670AGR02 | Start Date*: 2010-07-14 | |||||||||||
Sponsor Name:Novartis (Hellas) S.A.C.I | |||||||||||||
Full Title: A multicenter open label phase II study to evaluate the safety and efficacy of deferasirox in combination with deferioxamine followed by transitioning to deferasirox monotherapy in β-thalassemia pa... | |||||||||||||
Medical condition: Chronic iron overload in patients cardiac iron overload and β thalassemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000423-12 | Sponsor Protocol Number: CP506-001 | Start Date*: 2022-12-13 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Maastricht University | ||||||||||||||||||||||||||||||||||||||
Full Title: A modular, first time in human, open label, multiple dose, accelerated escalation with cohort expansion study of the safety and pharmacokinetics of intravenous infusion of CP-506, a tumor agnostic ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Tumour Agnostic treatment. ● Module differentiation: – Module 1 - monotherapy – solid tumour patients with cancer types that are enriched for HRD/FAD defects – Module 2 – combination with Carboplat... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001862-13 | Sponsor Protocol Number: AB19001 | Start Date*: 2020-03-12 | |||||||||||
Sponsor Name:ABScience | |||||||||||||
Full Title: A prospective, multicenter, randomised, double-blind, placebo-controlled, parallel groups, phase 3 study to compare the efficacy and safety of masitinib in combination with Riluzole versus placebo ... | |||||||||||||
Medical condition: patients suffering from Amyotrophic Lateral Sclerosis (ALS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Ongoing) SE (Restarted) GB (GB - no longer in EU/EEA) PT (Ongoing) ES (Restarted) PL (Ongoing) IE (Temporarily Halted) IT (Restarted) NO (Ongoing) GR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001447-39 | Sponsor Protocol Number: AB15003 | Start Date*: 2019-10-21 |
Sponsor Name:AB SCIENCE | ||
Full Title: A 24-week with possible extension, prospective, multicenter, randomized, double blind, placebo-controlled, 2-parallel group with a randomization 1:1, phase III study to compare efficacy and safety ... | ||
Medical condition: Smouldering or Indolent Severe Systemic mastocytosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) DE (Ongoing) PL (Ongoing) RO (Ongoing) LT (Completed) NL (Temporarily Halted) IT (Restarted) | ||
Trial results: (No results available) |
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