Pharmacodynamic and Clinical Evaluation of Dose and Taste-optimised Low Volume PEG-based Bowel Cleansing Solutions Using the Split-dosing Intake Regimen in Healthy Subjects and in Subjects Undergoing Screening Colonoscopy

Inclusion criteria

• The subject's written informed consent must be obtained prior to inclusion.
• Subjects age 40 to 70 years.
• Part B only: Subjects willing to undergoing a screening colonoscopy, where the subject:

• is between 40 and 70 years of age and has a known personal or familial risk of colon neoplasia,or
• is aged 55 to 70.
• Part A: Subjects need to be without any history of clinically significant gastrointestinal symptoms by clinical judgement and without the presence of acute abdominal discomfort or symptoms.
• Females of child bearing potential must be surgically sterile, post- menopausal, practicing true sexual abstinence or using an acceptable form of effective contraception throughout the study from the following list: contraceptive injections, implants, oral contraceptives, intrauterine system (IUS), some intrauterine devices (IUDs), vasectomised partner or barrier method (condom or occlusive cap) with spermicidal foam/gel/film/cream/suppository. Females using oral contraceptives must also use additional contraception. Hormonal and IUD methods of contraception must be established for a period of 3 months prior to dosing and cannot be changed or altered during the study. All females must have a negative pregnancy test at screening and check-in (unless post-menopausal).
• Willing, able and competent to complete the entire procedure and to comply with study instructions.
• Ferrous sulphate should be stopped at least one week prior to study medication.

Exclusion criteria

• Part A only: Subjects undergoing screening colonoscopy.
• Presence of current clinically significant functional gastrointestinal (GI) disorder (e.g. gastric emptying disorder, chronic constipation, irritable bowel syndrome [IBS]).
• Regular use of laxatives or colon motility altering drugs in the last month.
• Donation or loss of 500 mL or more of blood within 8 weeks prior to the first dose of investigational drug.
• Any history or current presence of ileus, gastrointestinal (GI) obstruction or perforation , GI tract cancer, inflammatory bowel disease (IBD) or colonic resection.
• Known glucose-6-phosphatase dehydrogenase deficiency.
• Known phenylketonuria.
• History or evidence of any clinical significant cardiovascular or neurological disease, cardiac, renal or hepatic insufficiency.
• Known hypersensitivity to polyethylene glycols and/or ascorbic acid.
• History or evidence of any clinically relevant electrocardiogram (ECG) abnormalities and/or uncontrolled hypertension.
• Evidence of dehydration.
• Any evidence for clinically significant abnormal sodium or potassium levels or other clinically significant plasma electrolyte disturbances.
• Females who are not post-menopausal with a positive pregnancy test. Females not using reliable methods of birth control if not post-menopausal.
• Clinically relevant findings on physical examination based on the Investigator's judgement.
• Clinically relevant deviations of laboratory parameters from reference ranges at screening or check-in evaluation.
• Positive serology for chronic viral hepatitis or human immunodeficiency virus (HIV) at screening.
• History of drug or alcohol abuse within the 12 months prior to dosing or evidence of such abuse as indicated by the laboratory assays conducted during the screening or check-in evaluations.
• Subjects who are unwilling to comply with the provisions of the study protocol.
• Concurrent participation in an investigational drug study or participation within 3 months of study entry.
• Subject has a condition or is in a situation, which in the Investigator's opinion may put the subject at significant risk, may confound the study results, or may interfere significantly.
• Previous participation in the study.
• Persons who are ordered to live in an institution on court or authority order