- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    10 result(s) found for: Water absorption.
                    
                
			
   			
		
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| EudraCT Number: 2013-002836-26 | Sponsor Protocol Number: DDD13POSA | Start Date*: 2014-01-09 | 
| Sponsor Name:KU Leuven - Drug Delivery & Disposition | ||
| Full Title: Gastrointestinal behavior of posaconazol in healthy human volunteers | ||
| Medical condition: Suspension: 105 mg posaconazol (2.6 ml Noxafil): 1)with 250 ml water 2)with 250 ml sparkling water 3)with 5 lumps of sugar, dissolved in 250 ml water 3)with 5 lumps of sugar, dissolved in 250 ml of... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-003248-28 | Sponsor Protocol Number: DDD22WATER | Start Date*: 2022-12-20 | 
| Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
| Full Title: The effect of sparkling water on the systemic pharmacokinetics of paracetamol in elderly | ||
| Medical condition: Healthy volunteers, 70+ years of age (administration of an antipyretic, analgesic drug) | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-001597-15 | Sponsor Protocol Number: MERLOT | Start Date*: 2016-12-19 | 
| Sponsor Name:Erasmus MC cancer institute | ||
| Full Title: Influence of a fatty beverage (Milk) on the absorption of erlotinib: a randomized, cross-over pharmacokinetic study (MERLOT-study) | ||
| Medical condition: Lung cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-003677-25 | Sponsor Protocol Number: 12I/T405 | Start Date*: 2013-01-27 | |||||||||||
| Sponsor Name:IBSA INSTITUT BIOCHIMIQUE SA | |||||||||||||
| Full Title: Safety and bioavailability of Tirosint (Levothyroxine Sodium) Oral Solution administered as single dose with or without water in hypothyroid patients. | |||||||||||||
| Medical condition: Both genders thyroidectomized patients, with thyroglobulin (Tg) circulating levels below 5 ng/mL and no evidence of Tg antibodies (Tg-Ab), at stable (at least 3 months) 100 μg/day levothyroxine ... | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004630-38 | Sponsor Protocol Number: HydroceleAlkScler | Start Date*: 2021-05-20 | ||||||||||||||||
| Sponsor Name:Region Jämtland/Härjedalen | ||||||||||||||||||
| Full Title: Sclerotherapy for hydro and spermatoceles with 99.5% Ethanol, an open clinical multicenter dose escalation study, phase 2 | ||||||||||||||||||
| Medical condition: Hydrocele and Spermatocele | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: SE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-003779-48 | Sponsor Protocol Number: D-CURE-IV-14-1 | Start Date*: 2014-10-13 | |||||||||||
| Sponsor Name:LABORATOIRES SMB S.A. | |||||||||||||
| Full Title: A phase IV, randomised, cross-over study to estimate the influence of food on the 25-hydroxyvitamin D3 serum level after vitamin D3 (D-CURE®) supplementation. | |||||||||||||
| Medical condition: Vitamin D deficiency (10-20 ng/ml) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003603-19 | Sponsor Protocol Number: Erlotinib_cola | Start Date*: 2014-03-11 | |||||||||||
| Sponsor Name:Erasmus University Medical Center | |||||||||||||
| Full Title: Influence of an acidic beverage on the absorption of erlotinib | |||||||||||||
| Medical condition: Lung cancer | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-005448-17 | Sponsor Protocol Number: TMC435HPC1010 | Start Date*: 2015-04-09 | |||||||||||
| Sponsor Name:Janssen Sciences Ireland UC | |||||||||||||
| Full Title: A Phase 1, open-label, randomized, 2-panel, 3-way crossover study in healthy adult subjects to assess the relative bioavailability of simeprevir following single dose administration of age-appropri... | |||||||||||||
| Medical condition: Chronic Hepatitus C Virus (HCV) Infection | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000438-35 | Sponsor Protocol Number: CL 0600-004 | Start Date*: 2004-09-30 | 
| Sponsor Name:NPS Allelix Corporation | ||
| Full Title: A study of the Efficacy and Safety of Teduglutide in subjects with Parenteral Nutritional Dependant Short Bowel Syndrome | ||
| Medical condition: Short Bowel Syndrome (SBS) refers to the clinical situation whereby a significant reduction in the absorptive capacity of the intestine results from inadequate anatomical or functional length of re... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-000176-11 | Sponsor Protocol Number: HM-GLP2-201 | Start Date*: 2021-12-20 | |||||||||||
| Sponsor Name:Hanmi Pharmaceutical Co., Ltd. | |||||||||||||
| Full Title: A Multicenter, Proof-of-concept, Phase 2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HM15912 in Adult Subjects with Short Bowel Syndrome-associated Intesti... | |||||||||||||
| Medical condition: Short Bowel Syndrome-associated Intestinal Failure (SBS-IF) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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