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Not yet recruitingNCT07583121COS-PBP-03Updated May 13, 2026

Impact of a Daily Application of an Omega-3 Monoglycerides Based Serum and Cream on the Skin Microbiota

An interventional study of Omega-3 monoglyceride based topical treatment in Eczema, sponsored by SCF Pharma. Not yet recruiting at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-13.

Sponsored by SCF Pharma · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

This exploratory study aims to investigate the prebiotic potential of daily application of an omega-3 serum and cream to skin affected by eczema. The study will also collect data on any potential adverse effects of the products. Ten subjects will be enrolled in the study and will receive the same treatment for fourteen days. Their baseline condition before treatment will serve as a control for the effects observed after treatment on the targeted eczema area. A second area of eczema treated with the patient's usual skincare routine will also serve as a control.

Read the detailed description

Omega-3 fatty acids, and Eicosapentaenoic acid (EPA) in particular, are known to promote the resolution of inflammation, unlike omega-6 fatty acids, which are pro-inflammatory. The skin, the largest organ in the human body, receives a high proportion of omega-6 fatty acids because skincare products are primarily composed of vegetable oils rich in omega-6. This imbalance could be one of the causes of inflammatory skin conditions such as eczema. Conventional omega-3s must pass through the digestive tract to be activated as monoglycerides. Therefore, their use in topical formulations is not practical. However, the recent development of pre-activated omega-3 monoglycerides finally opens the possibility of introducing active omega-3 fatty acids into moisturizing products.

All subjects will receive the same treatment for a similar duration. A skin area with eczema lesions will be identified during the screening visit. Subjects will be asked to apply the serum and cream to the clean, targeted area at least once daily for fourteen (14) days. The baseline condition before treatment will serve as a control for the effects observed after treatment on the targeted area. A second eczema area treated with the patient's usual care will also serve as a control.

Both targeted eczema areas will be used to measure the main study parameters:

  1. Quantify, by quantitative Polymerase Chain Reaction (qPCR), the four main bacteria of the skin microbiota (Staphylococcus aureus, Staphylococcus epidermis, Cutibacterium acnes, and Streptococcus pyogenes). Samples will be collected before the start of treatment (visit 1), as well as after one week (visit 2) and two weeks of treatment (visit 3).
  2. This study will also aim to collect data on any potential adverse effects of the products.
02

Conditions studied

  • Eczema

Keywords

  • Skin hydration
  • Skin inflammation
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Participant aged of at least 18 years old.
  2. Participant diagnosed with eczema who did not use corticosteroids in the 14 days prior to study day 1;
  3. Available for the entire duration of the study and willing to participate based on the information provided in the ICF duly read and signed by the latter.
  4. Participant without intellectual problems likely to limit the validity of consent to participate in the study and compliance with protocol requirements, having the ability to cooperate adequately, understand and observe the instructions of research staff

Exclusion criteria

Exclusion Criteria:

  • None
04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Experimental
    MagOX topic treatment

    Subjects will receive the daily treatment with MagOX serum and cream

    Other: Omega-3 monoglyceride based topical treatment

Interventions

  • OtherOmega-3 monoglyceride based topical treatment

    Successive daily application of omega-3 monoglyceride based serum and cream on skin with eczema.

05

What researchers measure

Primary outcomes

  1. To determine whether topical treatment with eicosapentaenoic acid monoglycerides can modulate the skin microbiota of eczema-affected skin

    Quantification of the skin microbiota by quantitative Polymerase Chain Reaction (qPCR) targeting the genome of four bacteria (Staphylococcus aureus, Staphylococcus epidermis, Cutibacterium acnes and Streptococcus pyogenes) on both treated and control skin area.

    Time frame: 2 weeks

Secondary outcomes

  1. Assessment of potential adverse effects of treatment

    An adverse event will be reported for any change observed by the research nurse or declared by the subject in the health of the treated skin area.

    Time frame: 2 weeks

06

Study locations

1 site
  • SCF Pharma
    Rimouski, Quebec G0K 1P0, Canada
07

References and documents

Individual participant data

Plan to share: No — The results of this research are the private property of SCF Pharma. If you are interested in the results of this study, you can contact Dr Samuel Fortin for a summary starting in summer 2027.

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07583121
Lead sponsor
SCF Pharma
Responsible party
Sponsor
First posted
May 13, 2026
Start date
May 4, 2026 (estimated)
Primary completion
Dec 4, 2026 (estimated)
Completion
Dec 18, 2026 (estimated)
Last update
May 13, 2026

Study contacts

Samuel Fortin, PhD, PhD
Contact
sfortin@scfpharma.com
418-750-8590
Anne-Julie Landry, M.Sc, M.Sc
Contact
ajlandry@ircl.ca
418-360-7480
Samuel Fortin, PhD
principal investigator · SCF Pharma

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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