Efficacy and Tolerability of a Topical Pigment-Correcting Serum in Melasma and Postinflammatory Hyperpigmentation

July 2026 | Volume 25 | Issue 7 | 596 | Copyright © July 2026


Published online June 29, 2026

Pearl Grimes MDa, Shanaya Dias BSa, Priscilla Huang BAb, Tsing Cheng PhDb, Elizabeth Makino BS MBAb

aVitiligo and Pigmentation Institute of Southern California, Los Angeles, CA
bAllergan Aesthetics, an AbbVie company, Irvine, CA

Abstract
Background: Melasma and postinflammatory hyperpigmentation (PIH) are common disorders of hyperpigmentation of key aesthetic concern. This study assessed the efficacy and tolerability of a serum formulated with lotus sprout extract, tranexamic acid, and niacinamide (LTN serum) for the treatment of melasma and PIH secondary to acne.
Methods: A 16-week, single-center, open-label study enrolled women (≥20 years of age) with mild to severe melasma or PIH. Participants applied LTN serum twice daily on the full face. Endpoints included assessments of overall hyperpigmentation, skin tone unevenness, and tactile roughness, modified Melasma Area Severity Index (mMASI), Mexameter measurements of melanin content in target lesions, Melasma Quality of Life Questionnaire (MelasQoL), participant self-assessment questionnaires, and tolerability.
Results: Of 30 female participants (n=15 per group), 57% self-identified as Black or African American, and 70% had Fitzpatrick skin types (FST) IV–VI. At week 16, significant decreases versus baseline were observed in both groups for overall hyperpigmentation (37% and 31% for the melasma and PIH groups, respectively; P<0.009 for both groups), skin tone unevenness (38% and 33%; P<0.008), and tactile roughness (67% and 52%; P≤0.005). mMASI and MelasQoL scores were significantly improved starting at week 4, with continuing significant improvement through week 16 (P≤0.05 and P>0.005, respectively). Mean change in melanin content was −36.5 at week 16 (melasma and PIH groups combined; P<0.0003). All tolerability parameters remained below mild.
Conclusions: The LTN serum is an effective treatment for improving melasma and PIH, particularly among participants with FST IV–VI.

 

INTRODUCTION

Hyperpigmentation is characterized by uneven skin tone, commonly due to excess melanin production.1 Hyperpigmentation is one of the most common dyschromias and is more prevalent in individuals with higher concentrations of melanin in the skin.1-3 Two common types of hyperpigmentation are melasma and postinflammatory hyperpigmentation (PIH).1,4 Melasma is characterized by tan-brown patches of pigmentation across the cheeks, nose, forehead, and other areas of the face.2 The development of melasma is caused by several factors, including genetics, UV and visible light radiation, and hormonal influences, including oral contraception, hormone replacement therapies, and pregnancy.5-7 PIH is an inflammatory hypermelanosis caused by a cutaneous inflammatory response, such as to acne, burns, picking of the skin, or certain cosmetic procedures.1,4 Melasma and PIH can have negative psychosocial impacts on individuals with either condition, including low self-esteem and emotional well-being.8,9

Both melasma and PIH are difficult to treat and often require a combination approach using topical agents and in-office procedures, including chemical peels, laser/light therapy, microneedling, and microdermabrasion.10,11 Despite the availability of treatments, achieving complete clearance in patients with melasma or PIH is challenging, particularly in individuals with skin of color, who naturally have higher concentrations of melanin in the skin. Thus, topical agents that are effective across a range of skin tones and capable of addressing multiple pigmentation conditions are warranted. To further these efforts, a serum formulated with lotus sprout extract, tranexamic acid, and niacinamide (LTN serum; Allergan Aesthetics, an AbbVie company, Irvine, CA) is now available for pigment correction.12 This study evaluated the safety and efficacy of the LTN serum over 16 weeks for the treatment of mild to severe melasma and acne-associated PIH.

MATERIALS AND METHODS

Study Design
A 16-week, single-center, open-label clinical study was conducted from February 2023 to September 2023. The study adhered to the Declaration of Helsinki and International Council for Harmonization Good Clinical Practice guidelines. An institutional review board reviewed and approved the study protocol at the center (Advarra IRB, Columbia, MD), and all participants provided informed consent prior to enrollment in the study.