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Melanotan-1 for Photoprotection: Dosing Comparison

Induction Phase (Clinical Trial Standard) 0.16mg/kg subcutaneous Every 48–72 hours for 10–14 days 10–14 days (visible pigment), 21–28 days (plateau) 30–45 days post-final dose Fastest pigmentation buildup; requires frequent dosing and strict adherence; standar

This comparison does not assign a generated winner or score.

  • Induction Phase (Clinical Trial Standard)
  • 0.16mg/kg subcutaneous
  • Every 48–72 hours for 10–14 days
  • 10–14 days (visible pigment), 21–28 days (plateau)
  • 30–45 days post-final dose
  • Fastest pigmentation buildup; requires frequent dosing and strict adherence; standard for research settings
  • Maintenance Protocol (Extended Use)
  • 0.08–0.12mg/kg subcutaneous
  • Once every 7–10 days
  • Assumes induction phase completed; maintains existing pigmentation
  • Sustained as long as dosing continues
  • Lower per-dose burden after induction; pigmentation fades within 30–60 days if discontinued
  • Controlled-Release Implant (Afamelanotide)
  • 16mg implant subcutaneous
  • Once every 60 days
  • 10–14 days (visible pigment), sustained release over 60 days
  • 60–90 days per implant
  • Eliminates frequent dosing; not available via compounding; used in clinical trials for EPP and PLE
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