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Dydrogesterone

孕激素 C

Dydrogesterone

Dydrogesterone

Oral

Dydrogesterone is a retro-isomer of progesterone with significantly higher oral bioavailability than micronized progesterone. Used as an alternative progestogen option in transfeminine HRT, though clinical evidence specific to transgender care remains limited [1] .

Dydrogesterone is a structural analog of natural progesterone with highly selective progestogenic receptor activity:

  • High oral bioavailability: ~28% (vs ~10% for micronized progesterone)
  • No anti-androgenic activity: Unlike CPA or spironolactone, does not directly affect androgens
  • No glucocorticoid or mineralocorticoid activity
  • Half-life: ~14-17 hours
FeatureDydrogesteroneMicronized Progesterone
TypeRetro-isomer (synthetic)Natural/bioidentical
Oral bioavailability~28%~10%
Sedative effectMinimalSignificant (hence bedtime dosing)
RoutesOral onlyOral/rectal/vaginal
VTE riskInsufficient dataNeutral or very low
Evidence levelCC
IndicationDoseNotes
HRT progestogen supplementation 10-20 mg/day Usually 1-2 times daily
Cyclic regimen 10 mg/day x 14 days/month Mimics luteal phase of menstrual cycle
BrandStrengthRegion
Duphaston10 mgWidely available globally (including mainland China)
Generics10 mgSelect regions
  • PRL (prolactin): Every 6 months. Progestogens may mildly elevate prolactin
  • No additional liver monitoring needed (dydrogesterone has very low hepatotoxicity)
  • Dydrogesterone allergy
  • Unexplained vaginal bleeding (cisgender indication — rarely applicable in trans context)
  • Acute hepatic porphyria