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MRB 0.3% Serum Effectiveness on 2 Early Clinical Markers of Photoinduced Cutaneous Aging: Actinic Lentigo and Actinic Keratosis

N

NAOS

Status

Unknown

Conditions

Actinic Keratosis
Actinic Lentigo

Treatments

Other: Topical application of MRB 0.3% serum and placebo serum (hemi face or skull)

Study type

Interventional

Funder types

Industry

Identifiers

NCT05152407
ID RCB 2020-A02883-36 (Other Identifier)
3020_ILS-MIRORU20

Details and patient eligibility

About

The aim of this study is to evaluate effectiveness of a serum containing 0.3% of MRB, a cosmetic active ingredient, against actinic lentigo and actinic keratosis.

Full description

Skin aging is an extremely complex multifactorial process that disrupts the functions and structure of epidermal and dermal cells and extracellular matrix components and has multiple causes including extrinsic phenomena (UV radiation, exposure to pollution, etc.).

It has important effects on the skin and is particularly apparent on the face. Indeed, sunlight, in particular ultraviolet light, is an important factor that contributes to cutaneous photoaging by inducing the photo-chronic generation of reactive oxygen species (ROS). Although skin has its own antioxidant system against ROS, these antioxidant defenses are not fully effective during sun exposure and weaken over time. Photoaging of the skin is characterized by the development of pigmentary disorders, such as actinic lentigos (AL), as well as benign skin tumors such as actinic keratosis (AK), both of which are target pathologies for this study.

AL usually occur in the elderly. They are usually benign but can cause aesthetic problems. They are commonly seen on the hands but can appear on all areas of the body, especially on sun-exposed areas such as the face, back, arms, feet, shoulders and skull. There are different treatment approaches, including physical therapy such as laser therapy, pulsed light, chemical peeling, bleaching and cryotherapy or topical therapy such as hydroquinone (HQ). Although topical therapies are generally more time consuming compared to physical therapies, patients can control their own treatment and side effects can be decreased.

AK is a very common skin lesion caused by chronic sun damage that typically measure less than 1 cm in diameter. KA is considered a premalignant epithelial skin lesion that may progress to squamous cell carcinoma. For this reason, all KA should be treated and clinical follow-up is recommended. The goals of treatment are: (i) to clinically eradicate obvious and subclinical lesions, (ii) to prevent their progression to EC, and (iii) to reduce the number of relapses and consequently increase the quality of life of patients.

Medical treatment with antioxidant properties/actions that would allow the reduction of damaged cells seems to play a role in both the prevention and treatment of AL and KA (Nashan et al., 2013).

In addition, a paper published in early 2020 highlighted a major role for carbonylation in the progression of this type of skin lesion (Tramutola et al., 2020). Based on these elements, we hypothesize that our cosmetic active ingredient - MRB - which has antioxidant activity and a specific and original chaperone effect giving it a strong capacity to fight against protein carbonylation- will be effective in the treatment of photo-induced signs of aging: keratoses and actinic lentigo, by a mechanism that acts on the oxidative stress pathway and the maintenance of cellular proteostasis.

Enrollment

35 estimated patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Minimum of 5 actinic lentigos and 3 actinic keratoses of grade 1 or 2 on each hemi-face of the face and/or hemi-cranium (in men with baldness)
  • Phototype I to III
  • Patients with free, informed, written consent to participate in the study.
  • Women unable to conceive or women of childbearing potential with a negative urine pregnancy test and using contraception

Exclusion criteria

  • Subjects with less than 5 actinic lentigos or less than 3 actinic keratoses of grade 1 or 2 on each hemiface of the face and/or skull (for men with baldness)
  • Phototype IV to VI
  • Immunocompromised subject
  • Subjects with a history of skin carcinoma in the treated areas
  • Subjects using another active treatment for actinic keratoses or lentigos (or having used one in the past 3 months)
  • Subjects unable to understand the information (due to language or psychiatric reasons)
  • Subjects without social insurance
  • Pregnant women
  • Breastfeeding women
  • Women of childbearing age without contraception
  • Subjects under legal protection measures
  • Subjects unable to express their consent
  • Subjects under legal protection

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

35 participants in 2 patient groups

Active serum on right
Experimental group
Description:
Right hemi face or skull will receive active serum (containing 0.3% MRB) / Left hemi face or skull will receive placebo serum for 6 months
Treatment:
Other: Topical application of MRB 0.3% serum and placebo serum (hemi face or skull)
Active serum on left
Experimental group
Description:
Left hemi face or skull will receive active serum (containing 0.3% MRB) / Right hemi face or skull will receive placebo serum for 6 months
Treatment:
Other: Topical application of MRB 0.3% serum and placebo serum (hemi face or skull)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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