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SkinMedica Lytera 2.0 Pigment Correcting Serum

Multi-target brightening with hexapeptide, tranexamic acid, and niacinamide

Duration
1 days2 sessions (朝・夜)
Downtime
なし
Sessions
8-12 weeks間で最適効果 (continuous推奨)

About This Treatment

SkinMedica Lytera 2.0 is an advanced brightening serum with multi-target approach without hydroquinone.

■ Hexapeptide complex: suppresses tyrosinase at gene expression level ■ Hexylresorcinol: melanin reduction (breaks down existing pigment) ■ Tranexamic acid: blocks UV-induced melanin via plasmin inhibition ■ Niacinamide: melanosome transfer inhibition + ceramide synthesis ■ Kojic acid: alternative depigmentation pathway

Validated in 10 clinical studies across 200+ subjects in US, Thailand, and Japan.

Mechanism of Action

Hexapeptide complex acts on TYR gene promoter to suppress tyrosinase mRNA transcription. Hexylresorcinol reduces/breaks down existing eumelanin. Tranexamic acid inhibits plasminogen→plasmin conversion, blocking UV→PGE2→MITF→tyrosinase cascade. Niacinamide attenuates PAR-2 signaling, inhibiting melanosome transfer 35-68%. Five mechanisms cover all stages of pigmentation.

Indications

Pigmentation / dullness

Expected Results

10 clinical studies across 3 countries (200+ subjects): 100% reported visible results by 12 weeks. Statistically significant improvements at 4, 8, and 12 weeks. Some improvement visible as early as 2 weeks. Effective for stubborn hyperpigmentation.

Clinical Evidence

SkinMedica Clinical Research (Allergan) (2019)
Lytera 2.0 Multi-Country Clinical Evaluation Program. SkinMedica Clinical Data
Clinical improvement was reported in this study (see original paper for details).
Desai S, Ayres E, Bak H, et al. (2019)
Safety and efficacy of a novel non-hydroquinone brightening serum in patients with facial dyschromia. J Drugs Dermatol
Clinical improvement was reported in this study (see original paper for details).
Hakozaki T, Minwalla L, Zhuang J, et al. (2002)
The effect of niacinamide on reducing cutaneous pigmentation and suppression of melanosome transfer. Br J Dermatol
Clinical improvement was reported in this study (see original paper for details).

Risks & Side Effects

Low risk. No ochronosis risk (hydroquinone-free). Rare transient mild irritation. Safe for all skin types and tones. Sunscreen recommended.

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