A Study in Healthy Adults to Compare the Bioavailability of EPA + DHA From Two Microalgal Sources to One Fish Source and Placebo
NCT07241377 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 120
Last updated 2026-04-29
Summary
This is a randomised, double-blind, parallel, placebo-controlled study in healthy adults to compare the absorption of two microalgal formulations, to a fish oil and a placebo. Participant will take their assigned study product for 6 weeks and attend the clinic for 4 visits.
Conditions
- Absorption of Omega-3
- Omega-3 Supplementation
- Healthy Participants
Interventions
- DIETARY_SUPPLEMENT
-
life'sTM omega O1035DS nTG
All Omega-3 oils will be diluted with high oleic sunflower oil for a total (EPA + DHA) content of 300 mg/capsule. Each subject will consume three capsules for a total intake of 900 mg (EPA+DHA)/day for 6 weeks.
- DIETARY_SUPPLEMENT
-
life'sTM omega O3020DS nTG
All Omega-3 oils will be diluted with high oleic sunflower oil for a total (EPA + DHA) content of 300 mg/capsule. Each subject will consume three capsules for a total intake of 900 mg (EPA+DHA)/day.
- DIETARY_SUPPLEMENT
-
MEG-3 3323rTG
All Omega-3 oils will be diluted with high oleic sunflower oil for a total (EPA + DHA) content of 300 mg/capsule. Each subject will consume three capsules for a total intake of 900 mg (EPA+DHA)/day.
- OTHER
-
Placebo
The placebo capsules will be a mixture of corn and soybean oils. 515 mg corn oil and 515 mg soybean oil. Each subject will consume three capsules a day.
Sponsors & Collaborators
-
DSM-Firmenich AG
collaborator UNKNOWN -
RDC Clinical Pty Ltd
lead INDUSTRY
Principal Investigators
-
Anne Birkett · dsm-firmenich Switzerland AG
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 64 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-10-27
- Primary Completion
- 2026-12-31
- Completion
- 2026-12-31
Countries
- Australia
Study Locations
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