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Andarine (S4)

Aliases: S-4 · Andarine · GTx-007

Last verified: 2026-09-23

DiscontinuedLimited evidenceSARMsLow interest

The short version

An early SARM — moderate anabolic strength, popular for cutting. Known for its signature side effect: yellow-tinted vision and night-vision problems. Key fact: Human data are limited: small trials or case-series reports exist, without large randomized studies. Preclinical + Phase I; development discontinued. Status: discontinued. Not approved; WADA-banned (S1).

Identity & type

Molecular type
SARM
Origin
An early SARM — moderate anabolic strength, popular for cutting.

Mechanism of action

Partial AR agonist; also binds ocular receptors (side effect).

not confirmed in humans

Dosing & routes

Official / clinical context

Development was abandoned; no active regulatory document exists. There are no official indications.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

Community: 25–50 mg/day (5 days on/2 off). Definition/vascularity in deficit phases; the characteristic "yellow" tint and slower dark adaptation at higher doses — reversible after discontinuation.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

Definition/vascularity in deficit phases; the characteristic "yellow" tint and slower dark adaptation at higher doses — reversible after discontinuation.

Protocol — official vs community

Official / label

No approved product. Development discontinued (vision side effects).

Duration:

Its metabolites bind retinal androgen receptors — the only SARM with a signature visual side effect.

Community (anecdotal)

25–50 mg oral daily, split AM/PM.

Cycle:
6–8 weeks.
Break:
6+ weeks.

The yellow-tint vision side is the community's self-limiting brake on dosing.

Human evidence

Human data are limited: small trials or case-series reports exist, without large randomized studies. Preclinical + Phase I; development discontinued.

Preclinical evidence

Preclinical + Phase I; development discontinued.

Known risks

  • Visual disturbances (reversible), suppression, liver enzymes.characterized
  • WADA prohibition (S1 anabolic agents)characterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Long-term human safety
  • Optimal dose and pharmacokinetics

Frequently asked questions

References

Systematic references are being expanded; verify sources directly before any decision.