Bioavailability of Omega-3 Food Supplement in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

August 31, 2014

Primary Completion Date

September 30, 2014

Study Completion Date

September 30, 2014

Conditions
Biological Availability
Interventions
DIETARY_SUPPLEMENT

Pronova Pure 150:500 EE EU

Each subject will participate in 4 treatment periods. The subjects are randomized to one of the following treatment sequences ABCD, BDAC, CADB, DCBA. 4 treatment free days between each treatment period

DIETARY_SUPPLEMENT

Pronovum PRF-037

Each subject will participate in 4 treatment periods. The subjects are randomized to one of the following treatment sequences ABCD, BDAC, CADB, DCBA. 4 treatment free days between each treatment period

DIETARY_SUPPLEMENT

Pronovum PRF-041

Each subject will participate in 4 treatment periods. The subjects are randomized to one of the following treatment sequences ABCD, BDAC, CADB, DCBA. 4 treatment free days between each treatment period

DIETARY_SUPPLEMENT

Eskimo-3

Each subject will participate in 4 treatment periods. The subjects are randomized to one of the following treatment sequences ABCD, BDAC, CADB, DCBA. 4 treatment free days between each treatment period

Trial Locations (1)

LS2 9LH

Covance Clinical research Unit (CRU) Ltd,Springfield House, Hyde street, Leeds

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pronova BioPharma

INDUSTRY