To determine the effect of investigational products on serum LDL cholesterol.

Inclusion Criteria:

• healthy mildly to moderate hypercholesterolemic (serum total cholesterol 5.2-8.5 mmol/l) adults
• signed written informed consent

Exclusion Criteria:

• participation in a clinical study within 30 days prior to screening visit and throughout the study
• severe obesity
• consumption of lipid/cholesterol lowering medication 1 month prior to the screening visit and throughout the study
• consumption of plant stanol or plant sterol containing food products such as Benecol or Becel pro active 1 month prior to visit 2