NCT01251822 Comparator Study of PEG 3350 Versus Prucalopride in Females With Chronic Constipation Status COMPLETED Phase PHASE3
NCT01251237 Study to Assess the Tolerability, Safety and Efficacy of an Adapted Gut Cleansing Solution in Routine Colon Cleansing Prior to Colonoscopies Status COMPLETED Phase PHASE2
NCT01175941 Effect of 7 Days of Dosing With a 10 mg Rectal Suppository of NRL001in Patients With Faecal Incontinence Status COMPLETED Phase PHASE1
NCT01164332 Sensitivity of Alternative NRL972 Detection Methods in Healthy Subjects Status COMPLETED Phase PHASE1
NCT01099683 Safety, Tolerability, Pharmacodynamic and Pharmacokinetics of a Single Rectal Application of 10 mg NRL001 in Elderly Subjects Status COMPLETED Phase PHASE1
NCT01099670 Safety, Tolerability, Pharmacodynamic and Pharmacokinetics of 7.5, 10, 12.5 or 15 mg NRL001 in a 2 g Suppository for 14 Days Status COMPLETED Phase PHASE1
NCT00915057 Effect of Chronic Viral Hepatitis on the Pharmacokinetics of NRL972. Status COMPLETED Phase PHASE2
NCT00896597 Reproducibility of Child-Turcotte-Pugh (CTP) Rating and NRL972 Pharmacokinetics in Patients With Cirrhosis Status COMPLETED Phase PHASE1
NCT00896246 Scintigraphic Assessment Following Klean-Prep® or Moviprep® Status COMPLETED Phase PHASE1
NCT00893607 Effect of Single Doses of 10 mg NRL001 Applied as a Suppository to the Anal Canal or Rectum Status COMPLETED Phase PHASE1
NCT00857480 Evaluation of the PK of NRL972 Following Pre- and co-Administration of Ursodeoxycholic Acid and Cloxacillin Status COMPLETED Phase PHASE1
NCT00857467 Study to Investigate Safety and Response to 1 or 2 g Rectal Suppositories Containing 5 or 10 mg NRL001. Status COMPLETED Phase PHASE1
NCT00856869 Clearance of NRL972 in Patients With Cirrhosis, Nonalcoholic Steatohepatitis (NASH) and in Healthy Volunteers Status COMPLETED Phase PHASE1/PHASE2
NCT00856752 Evaluation of the Pharmacokinetics of NRL972 Following Pre-Administration of Rifampicin and Cyclosporine Status COMPLETED Phase PHASE1
NCT00856713 Clearance of NRL972 in Patients With Cirrhosis and in Healthy Volunteers Status COMPLETED Phase PHASE1
NCT00850590 Study of Escalating Doses of NRL001 Given in Slow-release Rectal Suppositories of Different Weights Status COMPLETED Phase PHASE1
NCT00796354 Constipation Associated With Irritable Bowel Syndrome (IBS-C) Status COMPLETED Phase PHASE3
NCT00794716 PK of NRL972 in Patients with Nonalcoholic Steatohepatitis (NASH) and Non-Alcoholic Fatty Liver Disease (NAFLD) Status COMPLETED Phase PHASE2
NCT00794482 Multi-national Cirrhosis Study to Characterise the Association Between the Pharmacokinetics of NRL972 and Disease Severity. Status COMPLETED Phase PHASE3